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A PSYCHOGRAPHIC SEGMENTATION ANALYSIS OF PRESCRIPTION DRUG USERS A Thesis Presented to The Faculty of Graduate Studies of The University of Guelph by JULIE C . HORNE In partial fulfilment of requirements for the degree of Master of Science September, 1997 O Julie C. Home, 1997 National Library Bibliothéque nationale du Canada Acquisitions and Bibliographie Services Acquisitions et services bibliographiques 395 Wellington Street OttawaON K I A O N 4 Canada 395, rue Wellington OttawaON K1A ON4 Canada The author has granted a nonexclusive licence allowing the National Librxy of Canada to reproduce, Loan, distribute or selI copies of this thesis in microform, paper or electronic formats. L'auteur a accordé une licence non exclusive permettant à la Bibliothèque nationale du Canada de reproduire, prêter, distribuer ou vendre des copies de cette thèse sous la fome de microfiche/film, de reproduction sur papier ou sur format électronique. The author retains ownership of the copyright in this thesis. Neither the thesis nor substantial extracts fiom it may be printed or otherwise reproduced without the author's permission. L'auteur conserve la propriété du droit d'auteur qui protège cette thèse. Ni la thèse ni des extraits substantiels de celle-ci ne doivent être imprimés ou autrement reproduits sans son autorisation. ABSTRACT A PSYCHOGRAPHIC SEGMENTATION ANALYSIS OF PRESCRIPTlON DRUG USERS Julie C. Home University of Guelph, 1997 Advisor: Dr. J. Liefeld This thesis is an investigation of the information search activities of adult consumers of prescription dmgs. It identified distinct groups of consumers based on different patterns of attitudes regarding information search and prescription dnigs. Data were collected using a self-administered mail questionnaire in a s w e y of 456 prescription h g users, who indicated they had taken a prescription medication over the last 12 months. Eight underlying attitudinal dimensions were derived through Principal Axis Factoring of 32 attitudinal variables and were narned: information involvement, information avoidance. self-assured knowledge, self-care orientation, manufacturer-oriented information. doctororiented infonnation, pharmacist-onented information, and patient decision making. Using cluster analysis, the prescription dnig users were classified into different types according to the similarity of their scores on each of these eight attitudinal dimensions. The resulting typology formed three groups, each having a diffeferentonentation to infonnation search and prescription drugs. These were labelled the System Skeptics, the Confident Decision Makers, and the Uninformed Followers. Significant differences were found across the cluster groupings on a nurnber of behavioural. demographic and situational descriptors. Many thanks go out to my advisor, Dr. John Liefeld, my cornmittee members. Dr. KaRn Finlay and Dr. Dick Vosburgh. and my chairperson, Dr. Vinay Kanetkar for their guidance, patience and persistence with me - even after leaving graduate school to pursue full-tirne work in the field of market research. I would also Like to thank Market Facts of Canada Ltd. and Hoffinann-La Roche Ltd. for providing me with generous hnding for my research. My heartfelt appreciation goes out to my friends and farnily who never ceased to provide encouragement when it was need most. 1 would like to thank my father. Dr. John Home. in pa-rticular. for always finding time in his busy schedule io listen. to send a flurry of articles. e-mails or faxes,and for dways believing in me. Finally, 1would like to single out a very special person in my life. Pien Steel. who not only provided his love and encouragement, but laughter. a critical eye, statistical sawy. and even. exceptional writing skills. I know this has b e n a difficulijoumey. but 1do believe we have finally reached the end. Al! of my love goes out to you. TABLE OF CONTENTS I. INTRODUCTION 5 1.1 Problem Statement 1.2 Raîionaie 6 - - 7 II. LITERATURE REVTEW 8 2.1 Theoretical Foundations 8 2.2 Review of Previous Information Search Literature 2.2.1 Factors Influencing Extemal Information Search 2.2.2 Sumrnary 2.2.3 Typologies of Extemal Information Search 2.2.4 Summary 2.2.5 Review of Studies Related to Information Search for Drugs 2.2.6 Summary 10 II 16 16 20 20 26 2 3 Measures of External Search Behaviour 26 2.4 Methodologies Used in the Information Search Literature 28 3.1 Research Purpose and Objectives 31 3.2 Research Design 31 3 3 Questionnaire Development 33 3.4 Statisticai Anaiysis 34 3.4.1 Factor Analysis 3.4.2 Cluster Analysis 3.4.3 Cross-Tabulations 3.4.4 Discriminant Analysis 3.4.5 Multinominal Logistic Regession 34 36 38 39 40 3 5 Reseanih Assumptions 41 3.6 Research Limitations 41 IV.RESULTS 43 4.1 Introduction 43 4 2 Sample 43 4.2.1 Response Rate 4.2.2 Sample Characteristics 43 44 4 3 Factor Analysis 45 4.4 Cluster Anaiysis 56 4.4.1 System S keptics 4.4.2 Confident Decision Makers 4.4.3 Uninfomed Followers 4.5 Cross Tabulations 62 62 63 64 ... 111 4.6 Discriminant Analysis 4.6.1 Behavioural Measures as Predictors 4.6.2 Demographic Measures as Predictors 4.6.3 Situational Measures as Predictors 65 66 72 76 4.7 Logistic Regression 81 4.8 Muftinominal Logit 84 E DISCUSSION 5.1 Introduction 88 88 5.2 Attitudinal Dimensions 89 5.3 Psychographic Segments 5.3.1 Cluster # 1 - System Skeptics 91 - 5.3.2 Cluster #2 Confident Decision Makers 5.3-3 Cluster #3 - Uninformed Followers 5.4 Implications and Recommendations 5.5 Recommendations For Future Research 91 92 93 94 100 RFFERENCES 103 APPENDICES 108 APPENDIX 1: RESULTS FROM PRINCIPAL COMPONENTS ANALYSIS 108 APPENDIX II: RESULTS FROM PRINCIPAL AXIS FACTORING 114 APPENDIX III: RESULTS FROM HIERARCHICAL CLUSTER ANALYSIS 131 APPENDIX IV: RESULTS FROM NON-HIERARCHICAL CLUSTER ANALYSIS 142 APPENDIX V: RESULTS FROM DISCRIMINANT ANALYSIS 146 APPENDIX VI: RESULTS FROM LOGISTIC REGRESSION 168 APPENDIX VII: QUESTIONNAIRE 181 LIST OF TABLES Table 1: Principal Component., Analysis Factor Solution .............................................. 48 Table 2: Suggested Names For Principal Components Analysis Factoring Method Resulb ........................................................................................................... 49 Table 3: Principal Axis Factor Solution .8 Factor Solution............................................. 53 Table 4: Suggested Factor Names For Principal Axis Factoring Method Results ............54 Table 5: Reliability Coefficients for Composite Variables .............................................. 56 Table 6: Analysis of Agglomeration Coefficient for Hierarchical Cluster Analysis........ 57 Table 7: Mean Scores On Composite Attitudinal Scales For AI1 Prescription Dmg Users .................................................................................................................. 57 Table 8: Results of Non-hierarchical Cluster Analysis with Initial Seed Points frorn Hierarchical Results .................................................................................................. 59 Table 9: Mean Scores on Attitudinal Variables Used in Cluster Analysis....................... 60 Table 10: Ever Asked Doctor to Prescribe Specific Medication...................................... 64 Table 11: Ever Asked Phamacist For Genenc Substitution............................................ 65 Table 12: Canonical Discriminant Functions For Behavioural Variables........................ 66 Table 13: Canonical Discriminant Functions Evaluated At Group Means ...................... 67 Table 14: Results of Discriminant Function Analysis of Information Search Behaviour 68 Table 15: Group Means by Redictor Variables............................................................... 69 Table 16: Classification Results for Behavioural Predictors............................................ 70 Table 17: Classification Results for Cases Selected for Use in the Analysis ................... 71 Table 18: Classification Results for Cases Not Selected for Use in the Analysis ............ 71 Table 19: Classification Results for Demographic Predictors ......................................... 72 Table 20: Canonical Discriminant Fumions ................................................................... 73 Table 2 1: Canonical Discriminant Functions Evaluated At Group Means ...................... 73 Table 22: Results of Discriminant Function Analysis of Demographic Variables .......... 75 Table 23: Group Means by Demographic Predictor Variables ........................................ 76 Table 24: Canonical Discriminant Functions For Situational Variables .......................... 77 Table 25: Canonical Discriminant Functions Evaluated At Group Means ...................... 77 Table 26: Results of Discriminant Function Analysis of Health Characteristics ............. 79 Table 27: Group Means by Predictor Vanables ............................................................... 80 Table 28: Classification Results for Situational Predictors ..............................................80 Table 29: Classification Results for Cases Selected for Use in the Analysis ...................81 Table 30: Classification Results for Cases Not Selected for Use in the Analysis ............ 81 Table 3 1: Classification Matrix Using Demographic Indicators to Predict Group Mem bership ............................................................................................................... 83 Table 32: Classification Mauix Using Demographic Indicators to Predict Group Mem bership ............................................................................................................... 83 Table 33: Classification Matrix Using Dernographic Indicators to Predict Group Membership...............................................................................................................84 Table 34: Predicted Percentages Based on Coefficients from LIMDEP Output..............87 I. INTRODUCTION As part of the process of consumer decision-making, consumers generally recognize a problern or unmet need and may undertake an information search. prior to purchase, to resolve these problems (Stemthal & Craig, 1982). During the information searching stage, both intemal and extemal search can take place. Interna1 searching occun when information is accessed from an individual's long-term memory, whereas externai seanih occurs when information is actively puaued from extemal sources (Bettman, 1978). While prior studies have lacked a consistent definition of what behaviours constitute extemal information search. such definitions as the nurnber of informational sources from which information was sought the arnount and types of information sought, the time allotted to searching for information, as well as the number of brands for which information was sought, have been used to charactenze consumers' extemal information seeking behaviour (Kiel & Layton. 1981). For the most part. the literature on consumer information search has suggested that there are rather distinct patterns of searching behaviour, but has largely focused on the information searching behaviours of purchasers of durable goods (Newman & Staelin, 1972; Claxton. Fry & Portis, 1974; Westbrook & Fomell, 1979; Kiel & Layton, 198 1 ; Furse, Punj & Stewart. 1984). This study, however, will extend the existing literature into the information search behaviours for prescription dmgs by adult consumes. Although the literature in the area of information search patterns for prescription dmgs is limited, the few studies that have been conducted to date have tended to focus on consumers' experiences with various health professionals and the information provided by these professionals. Little emphasis has been given to the information sought out by consumers themselves, and the underlying reasons why these consumers may, or may not, search for drug information. Morris, Grossman. Barkdoll, & Gordon (1987), however. examined the information search behaviours of recent purchasers of prescription drugs. Four distinct groups of consumers were categorized according to their search behaviours: physician reliant, pharmacist reliant, questioners and the uninfonned. Another study examined the information search motives of elderly users of hypertension medication (Moms, Tabak & Olins, 1992). Four segments of information seekers were identified as: ambivalent learners, uncertain patients, ris k avoiders, and the assertively self-reliant. 1.1 Problem Statement Understanding the search activities of prescription dnig consumers requires examining how these consumers, if at dl, go about gathering information about their prescription medications. Of particular interest is from where the information is obtained (Le. physicians, pharmacists, interpersonal contacts with frienddrelatives. or extemal resources such as reference books, magazines, TV etc.), and consumers' motives for seeking out dmg information (e.g. self-care. desire to communicate better with physician, inability to obtain enough information irom health professionals, etc.). In addition to the absence of descriptions about consumen' information search behaviours for dmg information, no Canadian published nor publicly-held studies have been conducted on consumers' search activities for drug purchases. The few studies that have been reported were done in the United States. 1.2 Rationale At present, the Ministry of Health in Ontario, as well as other provincial ministries, are undertaking reform of drug programs with the airn of "enabling consumers to get al1 the information they need about their drugs and to undentand how to get that information" (Ministry of Health, 1994. p. 20). Therefore, a study related to consumers' search patterns for drug information appears to be needed in order to most effectively target informational materials and educational prograrns to these consumers. In addition. this study will potentially offer guidance to marketing practitioners in their efforts to se11 dnig products. Dmg information may be targeted and disseminated to consumen who are receptive and who are actively involved in their prescription medication decisions. Also, the identification of such information search patterns could potentially assist retailers (e.g. chain drug stores, independent pharmacies) in providing better customer service. By offenng drug information to receptive consumers, they may give themselves an advantage over cornpetitors who lack such a service. Finally, this study will contribute to the existing information search literature by expanding beyond durable goods into consumers' search for information about prescription dnigs. The information search activities of prescription drug users will be analyzed to identify a typology of information search behaviours. This typology will be profiled using behavioural, demographic. and situational descriptors in order to aid in the identification and understanding of the groups. II. LK'ERATURE REVIEW 2.1 Theoretical Foundations As part of the conceptual models of consumer decision-making. information search is conceptualized as a sub-cornponent of the decision process. Most decision models postdate a sequence of steps that involve identifying a problem to be solved; gathenng information about alternative courses of action; evaluating and weighing the opaons; choosing an alternative; and taking action to solve the problem. The notion that consumers may undertake an extemal search for information prior to a purchase decision has been widely popularized by conceptual models such as those of Engel, Kollat and Blackwell (1973) and Bettman (1979). A discussion of these two conceptual models will be provided in order to contextualize the information search component within the overall consumer decision-making process. One of the most widely-used models for understanding consumer behaviour was developed by Engel, Kollat and Blackwell(1973). This mode1 provides a general representation of consumer behaviour, which encompasses the information search component. In particular. this mode1 hypothesizes a five-stage decision process which includes: problem recognition, search, alternative evaluation, choice and outcorne. In the context of information acquisition. the EKB mode1 defines search as a "motivated exposure to information with regard to a given alternative resulting when existing information, beliefs and attitudes are found to be inadequate" (Engel. Kollat & Blackwell, 1982. p. 321). As stated by Engel, Kollat and Blackwell (1973), the factors that most often motivate a consumer to undertake an external search for information occur when the quantity and quality of existing information is insufficient. when information is not readily recalled frorn rnemory, when perceived risk is high (price, social or physiological risk). or when the consumer experiences uncertainty about their own ability to make a correct choice. While this mode1 is useful in identifying variables that inff uence the consumption process and in providing a framework for examining anas of consumer behaviour, the EKB model has not been ernpirically tested. Therefore. the EKB model is only useful for suggesting relationships among variables, rather than for providing conclusive evidence about these relationships (Horton, 1984). In addition to the EKB (1973) model, one of the most comprehensive theones of information search, based on an information processing perspective. is provided by Bettman (1979). In Bettman's model, intemal and extemal search processes are outlined and are further distinguished by the direction and degree of information search taken by consumers. Direction of external search refers to the type and source of information sought by consumers. while degree of extemal search refers to the amount of information sought (Bettrnan, 1978). The factors influencing the direction of extemal information search are noted by Bettman as: the current goals of the consumer (Le. what information is useful for the choice at hand). prior experience/stored knowledge (i.e. what is already known) and the structure of the environment (i.e. what is available in the extemal environment). On the other hand, the influences upon the degree of search are outlined as: the costhenefit of searching for information, choice environment factors (Le. information availability, difficulty of the choice, time pressure). individuals differences. and the level of conflict or uncertainty about the decision (Bettman. 1978). The first section of the literature review covers the factors influencing the degree of extemal infomation search undertaken by consumers. while the second section reviews the studies that have developed typologies for understanding infomation search patterns. The third section coven research related io the area of information search behavioun for prrscnption drug information. The fourth. and fifth sections address the measures that have been used in previous studies to represent extemal information search. and the various methodologies that have been used in the examination of information search. 2.2 Review of Previous Information Search Literature For the most part, existing studies on search behaviour have tended to focus on developing typologies of search strategies, or on the explanatory factors that influence search behaviour. A problem in the literature, however, is in the diversity of the determinants exarnined and in the analytical methods used throughout the research, which makes it difficult to draw cornparisons among the studies. Some researchers have examined predictoa of various kinds of search behaviour, while other approaches have used cluster analysis to determine distinct pattems of search behaviour (Claxton. Fry & Portis, 1974; Newman & Staelin, 1972; Westbrook & Fornell, 1979; Kiel & Layton, 1981; Furse, Punj & Stewart, 1984). 2.2.1 Factors influencing Extemal information Search A number of determinants of external search have been examined in the information search literature, which centre primarily on the search activities undertaken for durable goods. In their review of the literature, Beatty & Smith (1987) outlined seven categones of variables that affect search: market environment; situational variables, potential payoff, knowledge and experience: individual differences; conflict and conflict resolution; and cost of search. Approxirnately 60 variables have been studied empirically as determinants of search (Beatty & Smith, 1987; S ~ i v a s a n& Ratchford. 1991). Newman (1977). in his review of the literature, outlined a number of determinants of search that have been examined. Previous purchase history, demographic background, buyer personality. perceived risk, and perceived costs of search are the major categones of deterrninants that have been shown to be related to external information search. Other studies have examined a host of variables that are related to the tendency for consumers to engage in search. Using an involvement-based perspective, Beatty and Smith (1987) studied the relationship between external search effort and a number of motivating antecedent variables, such as ego involvement, product class knowledge, time availability. purchase involvement and attitudes toward shopping. Extemal search effort, on the other hand. was represented by a total search index based on four major dimensions of search: media search, retailer search, interpersonal seamh and neutral sources. Using self-report measures from recent purchasers of televisions, VCRs. and home cornputers, the results indicated that greater retailer and media search were both associated with higher purchase irivoivementlshopping attitudes, greater time availability and lower product class knowledge. For the interpersonal search component (Le. seeking the opinions of others), product class knowledge appeared to be the primary motivator. Purchase involvement/shopping attitudes also had a significant influence on interpersonal search. For neutral sources, time availability and ego involvement were the only two variables associated with this fonn of extemal information search. Newman and Staelin (1972), on the other hand, examined the amount of information search undertaken by buyers of new cars and major household appliances. Using a combined score of in-store and out-of-store activities into an overall search index, Newman and Staelin (1972) found that the number of brands initially considered. whether the same brand was bought as before. the identity of the household member exercising the most influence on the decision. the consumer's ability to judge the product. education. and stage in the life cycle to be significant predictors of search at the .O5 level. Three others variables were significant at the .IO level, location of the household by city size, the occupation of the head of household. and the number of times the product was purchased in the last ten years. Using self-reported rneasures. Duncan and Olshavsky ( 1982) studied the relationship between consumer beliefs about the marketplace (e.g. "1 need to look at al1 the available choices if I am to tell which is the best one") and the pre-purchase extemal search behaviours of recent purchasers of colour televisions. Similar to the measures used by Newman & Staelin (1972). an index of in-store activities such as the number of stores visited and number of brands examined, and out-store activities such as the number of times infomation was sought from personal sources. unsponsored sources and marketing dominated sources were used to charactenze extemal search. The results of the study indicated that beliefs about the marketplace and an individual's view about their capabilities as consumers accounted for 50 percent of the variance in extent of extemal search. Duncan and Olshavsky (1982) concluded that the large percentage of variance explained by the beliefs suggest that they are an important determinant of external prepurchase information seeking. Using a behavioural process methodology. Moore and Lehmann (1980) conducted an information acquisition experiment on the purchase of bread, a low-involvement good. Moore and Lehmann ( 1980) classified the deterrninants of external search into six categories: market environment, situational variables. potential payoff/product importance, knowledge and experience. individual differences and conflict and conflictresolution strategies. Extemal search was charactenzed in terms of total number of acquisitions, number of brands searched, and the number of amibutes searched. Regression analysis showed that only time pressure (situational), knowledge/expenence and ability (individual) were significantly related to total search. Swan (1969) studied the relationship between consumer learning and the extent of information search using a senes of choice situations involving hypothetical brands of shirts. He proposed that infomation seeking would decline with repeated choice of the same brand, and with the choice of a satisfactory rather than an optimal choice. The results frorn Swan's study indicate that expenence with the brand and a satisfactory choice as the decision objective leads to lower information seeking behaviour. Schaninger and Sciglimpaglia ( 198 1) examined the relationship between cognitive peaonality traits and demographics on depth of search (the number of cues drawn and number of dimensions exarnined) using a behavioural process methodology. Six traits were used to represent individual differences in information processing: tolerance for ambiguity. rigidity, cognitive style, need for cognitive clarity, self-esteem and trait anxiety. Age, family life cycle, and socio-economic factors were used as demographic variables. The findings suggest that individuals who were younger. earlier in the farnily life cycle. educated, and of higher social class examined more cues and alternatives under the hypothetical buying decisions. Furthemore. those individuals who were tolerant of ambiguity, had clarifier cognitive styles (i.e. seek additional information to clarify understanding), and had higher self-esteem exarnined more cues and alternatives in the hypothetical buying decisions. Bnicks (1985) studied the effects of prior knowledge about a product class on pre- purchase information search. Brucks (1985) concluded that knowledgeability encornpassed both objective and subjective dimensions. Objective knowledge referred to what an individuai actually knows. while subjective knowledge referred to an individual's degree of confidence in hisher knowledge. A number of studies, however, have found a negative relationship between amount of product experience and arnount of extemal search (Moore and Lehmann, 1980; Newman and Staelin, 1972; Swan. 1969). A common explanation for the negative relationship between knowledge and search is that expenenced consumers have existing knowledge about the various attributes of various alternatives, and consequently do not need to acquire such information from external sources. However, another cornmonly held explanation asserts that expenenced consumes perform more efficient searches for information because pnor knowledge may aliow the individual to distinguish, formulate and evduate information more efficiently. A number of studies have postulated that prior knowledge encourages information search by making it easier to process information (Punj & Staelin, 1983). Although the results are ofien contradictory. the findings from Brucks' study indicate that pnor knowledge facilitates the acquisition of new information. A study by Urbany, Dickson and Wilkie (1989) examined the relationship between consumer uncertainty and the extent of infonnation search behaviour using purchasers of major household appliances. Extemal search was charactenzed according to measures of the amount of time spent shopping, the number of different stores shopped at, the number of brands considered, and the use and reactions to various sources of information. Urbany et al. classified uncertainty into two dimensions: knowledge uncertainty (i.e. what is known about the alternatives) and choice uncertainty (Le. which alternative to choose). From the results, it was found that choice uncertainty tended to increase search, whereas knowledge uncertainty had a negative effect on search. It was hypothesized that greater knowledge uncertainty was associated with a reduced ability to eficiently use new information making infonnation search a more difficult process. For choice uncertainty, it was argued that this type of uncertainty produced conflict and. subsequentiy, the motivation to resolve that conflict. Therefore, more extensive search was undertaken by those experiencing choice uncertainty than those experiencing knowledge uncertain ty. While it is usehl to examine the explanatory variables that are related to consumers' information search activities, these results are limiting as they tend to examine a few determinants of search behaviour against a diversity of measures used to characterize extemal search. Measures such as the counts of retail shopping activity, sources and types of information used, alternatives considered, time spent in the purchase decision process. and a total search index have al1 been used to rcpresent external search (Newman, 1977). Therefore, a lack of consistency in the definitions of search makes it difficult to draw conclusions about which variables affect the external search undertaken by consumers. Furthemore, the variables found to be significantly related to search in bivanate tables frequently fade into insignificance when multivariate techniques are used, and the amount of variance explained by any one variable has typically been small. In his review of the literature, Newman (1977) stated, "The relationship between arnount of search and any one determinant seldom has been drarnatic. Differences in group means typically are small and the diversity of behaviour within groupings of buyers is the rule, reflecting the complexity of influences on behaviour". (p.32) 2.2.3 Typologies of Extemal Information Search While researchers have typically sou& to detemine the amount of search conducted by consumen, as well as to identify the major influences on search. other studies in the area of information search have sought to develop distinct segments or clusters of consumers based on their information search patterns. Early efforts to identify distinct groups of consumers characterized by differing information search patterns used unidimensional measures of aggregate search activity. These aggregate measures. however, have been cnticized for failing to adequately define differences in patterns of information gathering. Recent studies have distinguished information search patterns according to the type of sources used, such as retailer, media and interpenonal search. while others have distinguished search patterns according to information. brand and time dimensions. Using canonical correlation analysis, Westbrook and Fomell ( 1972) studied the degree of information seeking by consumers of new cars and major household appliances. Measures of retail, neutral and personal sources were used as criterion vanables and six explanatory measures as predictor variables (age. education. satisfaction. working order of previously purchased product, joint decision making and number of brand alternatives). The first canonical variate was interpreted as the extent of physical shopping search, and was associated with the number of brand alternatives considered. higher education. and the absence of an urgent need to replace the product. On the other hand, the second canonical variate was interpreted as the tendency to seek out objective (neutral) versus subjective (personal) pre-purchase information, and was negatively associated with buyer age and education. Following this, four segments of consumers were denved according to the types and intensity of usage of different information sources during their recent purchase expenence: "objective shoppers" (reliance on neutral sources to the exclusion of persona1 sources), "store intense shoppers" (high degree of retail search and greater consultation with penonal sources. " personal advice seekers" (visit few retail outlets and rely on friends, neighbours and relatives) and "moderate shoppers" (visit the fewest retail outlets and do not rely on neutral or personal sources). Kiel and Layton (198 1). on the other hand, conducted a study of the behaviours and correlates of information search activities for new automobile buyers. Measures such as the number of dealers visited. the number of ads recalled, the amount of time spent searching for information, and the number of phone calls made were used as measures of search behaviour. Using principal factor analysis. four factors emerged as the dimensions representing various search behaviours: retail search. media search, interpersonal search and a time dimension. To develop a taxonomy, cluster analysis produced three major search groups: high information seekers, low information seekers, and selective information seckers. Using rank order correlation and t-tests, the examination of the correlates of search behaviour siiggested that only certain predictors of search behaviour were related to the search dimensions. Relationships emerging from this research suggest that continuing exposure to product information via low-involvement learning leads to greater information search dunng the decision period; consumen with the Ieast selfconfidence in decision-making undertake the greatest search activity; and search activity tends to decrease with age. A snidy conducted by Furse, Punj and Stewart (1984) identified distinctive extemal information search patterns among purchasers of new automobiles. Extemal information search behaviour was measured according to: the number of dealers visited, the activities at the dealerships visited. and out-of-store information search behaviour (talking to friends, reading magazines). Other variables included the number of previous cars owned, satisfaction with the car purchased, and selected demographic information. Using principal cornponents analysis, five factors emerged as the dimensions representing extemal search behaviour: retailer visits, out-of-store search. interpersonal search, instore search, and the involvement of others. Using the factor scores as the basis for the cluster analysis, six clusters were denved: a low-search group, a purchase-pal assisted group. a high search group, a high self-search group, a retailer shopper group and a moderate search group. Claxton, Fry and Portis (1974) classified consumers of fumiture and major appliances in ternis of their information gathenng activities. According to Claxton et al., three classes of variables were viewed as potential causes of search pattern differences individual, situational and product characteristics. Similar to other studies researching extemal search, information search was measured by: the type and range of alternatives considered, information sources used, features considered, stores visited and time spent considering the purchase (Newman & Staelin, 1972). From the resulü, three mesures were found to generate distinctive clusten: number of information sources used, total visits to stores and deliberation time. The three clusters obtained in both the furniture and appliance samples were labelled thorough (store intense), thorough (balanced) and nonthorough. income, education and concem with selecting the right product were positively associated with thoroughness, whereas situational characteristics such as immediacy of need and financial constraints were negatively and positively nlated to search. 2.2.4 Summary By developing typologies of information seanih patterns, different groups of consumers can be identified according to the search behaviours exhibited by them. A shortcoming in this research, however, is that the studies conducted have focused pnmarily on the information search behaviours in which consumers engage in. without examining the underlying reasons why these consumers seek out information fiom external sources. Furthemore, the information search patterns that have emerged have tended to examine only the search behaviours for purchasers of durable goods. Information search patterns for other product classes have received considerably less attention in the research. 2.2.5 Review of Studies Related to Information Search for Dmgs Although a substantial amount of research has been conducted on the prepurchase search activities employed by consumers of durable goods. little ernpincal research has been conducted on the information sought by consumers in decisions involving their health. While engaging in information search is acknowledged to be one mechanism by which consumers cope cognitively with uncertainiy surrounding healthrelated events. then is evidence to suggest that consumers ofien perceive that they are unsuccessful in obtaining the necessary information, particularly from health professionals. despite their desire to acquire health-related information (Lenz, 1984). Thus, greater attention needs to be given to attitudinal dimensions that may inhibit or facilitate consumers to engage in a search for information about their drugs. A study conducted by Morris. Grossman, Barkdoll and Gordon ( 1987) examined the source and nature of drug information received and sought by consumers in conjunction with a prescription obtained within the previous four weeks. Experiences at the pharmacy, such as what was said about the medication (i-e. how much medication to take or use; how ~ f t e nto take or use the medicine; whether or not the medication could be refilled; any precautions to take while using the medication; as well as any possible side effects). whether this information was provided by the phamacist or if the consumer had to ask about it. as well as the printed or audio-visual materials available were used to represent the sources and nature of dmg information obtained at the pharmacy. Similar measures were used to represent the consumer's experiences at the physician's office. with the inclusion of a measure to indicate the various individuals who may have provided information to the consumer (i.e. doctor. nurse. secretary or technician). In addition to the experiences at the pharmacy and at the doctor's office, consumers were asked to indicate which self-initiated information search activities they engaged in. such as reading reference books, magazines. newspapen, or taiking to fnends or family. As an attitudinal component, consumers were also solicited about their attitudes towards various barriers (e.g. "It is difficult to get information because the doctor uses technical terrns) or facilitators (e.g. "It would be easier to ask questions if you thought of some questions and wrote them down before your appointment) in obtaining information from the doctor and phamacist. Factor analytic and clustering techniques were used to segment consumers according to the sources and nature of drug information obtained by thcm. Using principal components analysis, four factors represented the sources of information, and were interPretable': 1) non-health professional sources, 2) spontaneous counselling activities of physicians, 3) spontaneous counselling activities of pharmacists and. 4) question asking activities directed to both the doctor and pharmacist Factors scores were used as input into the cluster andysis, and the four clusters retained were: physician reliant, pharmacist reliant, questioners and the uninfomed2. In order to provide a descriptive portrayal of who these consumers were, the four groups were compared for demographic. situational and attitudinal differences. The uninformed segment were the least likely to actively pursue information. were likely to perceive several informationseeking barriers. and were most apt to see trust in the physician as negating the need to obtain information. The physician-reliant group, on the other hand. were apt to be passive recipienü of physician-supplied information. who responded favourably to counselling, perceived few baniers to obtaining infornation from the physician, and reported self-initiated search made them feel better. The questioners were most likely to consult reference books and magazines and perceived multiple barriers to obtaining information from health professionals; whereas the pharmacist-reliant group were the least likely to obtain information from references books or magazines. The pharmacist- I e" Arnount of variance explained by each factor was not reported. structure was viewed to be stable as the sarnple was randomly split and the four-cluster soiution was similar for each of the haIves. reliant group, however. were the most responsive to both counselling from the doctor and the pharmacist, but tended to receive counselling at the pharmacy to a greater extent While this study provides a description of the information seeking behaviours of consumen of drugs based on the activities at the pharmacy. physician's office and at a self-initiated level, Moms et al. (1987) suggested that future studies could potentially include lifestyle. health beliefs, and psychographic variables in order to provide a more thorough description of the clusten. Another study conducted by Moms, Tabak & Olins (1992) studied the infonnation seeking motivations of elderly users of hypertension medication. Information conceming health beliefs, motivations and preferences for infomationseeking and active participation in healthcare were addressed in the research, along with perceptions of knowledge, and demographic information. Using exploratory factor analysis, six factors best described the rnoûvational bases for information searsh. These were 1) information involvement. 2) self-care, 3) regimen barriers, 4) information avoidance, 5) risk aversion, and 6) question-asking. The factor scores served as input into the cluster analysis. The results indicated four distinct segments of infonnation seekers: ambivalent leamen, who viewed themselves as vulnerable to negative health infonnation. not particularly healthy, but receptive to drug information; uncertain patients, who perceived dificulty adhenng to the drug regimen and reported low levels of information receipt from health professionals; nsk avoiden, who viewed infmnation-seeking as a risk-coping strategy; and the assertively self-reliant. who were the least receptive to information about their medication. While distinct market segments have been identified by Moms et al. (1987) according to their information-seeking strategies and their underlying motivations. age has also been shown to be a significant predictor of the amount. and type. of information obtained by consumers. A study by Morris, Grossman. Barkdoll. Gordon and Chun (1987) has shown that the elderly seek less information from health professionals about their drugs than their younger counterparts. despite the fact that the elderly are most in need of such information. Morris et ai (1987), however, suggested that this may be due to the type of condition being treated among the eldedy. For the most part. elderly patients consume medications for chronic rather than acute illnesses. Thus, the nature of the information provided rnay Vary depending upon the condition being treated. Moms et al. (1987) suggested that the elderly may obtain information over a longer period of time than their younger counterparts due to the nature of their illnesses. However, this explanation is only speculative as the respondents included in this study were only eligible to participate if they had obtained one or more new (e.g. non-refill) prescriptions in the last four weeks. Thus, those consumers taking prescription drugs for chronic illness were excluded from the analysis. In terms of the nature of the information provided. younger consumers were more likely to receive information about the side effects of their drug purchases than the elderly (Moore, Kalu, Yavaprabbas, 1983; Moms et al., 1987). A statistically significant difference (p < .0001) also existed between self-initiated searches for information among elderly and non-elderly subjects. Younger subjects were more likely to consult friends and relatives about their prescription. while the elderly were more likely to report that ?heyobtained information about their prescription from mass media sources such as magazines. newspapers. television and radio. While not specifically related to prescription dmg usen. a study conducted by Stnitton & Lumpkin (1992) examined the differences in information search behaviour among eldedy adoptes and non-adopters of healthcare innovations. Of particular interest in this study was the product category of generic dmgs. Innovativeness was measured on two dimensions: the innovation's perceived effect on one's daily routines, and the respondent's usage of the product. Information search, on the other hand. was characterized by marketer-dominated sources (e.g. point-of-sale information). interpersonal sources (e.g. spouse, fnends, neighbours), medical expert sources (e-g. docton, pharmacists), independent expert sources (television programs. magazine and newspaper articles) and mass media sources (e.g. television. magazine and newspaper advertisernents). Compared to nonadopters, the results suggested that adopters placed more importance on interpersonal sources, independent expert sources and medical expert sources as potential sources of information for genenc dmgs. However, the relative importance of each information source type for both adopters and nonadopters were: medical experts, interpersonal, marketing-dominated, independent expert sources, and the mass media. Strunon & Lumpkin (1992) noted, however, ihat the nurnber of sources evaluated as "important" among both adopters and non-adopters were relatively small, which suggested that information search. even for a health-reiated purchase, is a relatively limited activity. 2.2.6 Summary While typologies of the information search behaviours, and motives of prescription drug users have been developed, greater emphasis needs to be given to the attitudinal or psychographic dimensions inhibiting or facilitating information search for prescription dmg information. If unique groups of prescription drug users exist. this will aid in the development of informational materials and educational programs targeted to these consumers. 2.3 Measures of External Search Behaviour A variety of rneasures have been used to define extemal search behaviour (Beatty & Smith, 1987; Kiel & Layton, 198 1; Moore & Lehmann, 1980; Newman & Staelin. 1972). However. a consistent definition of what behaviours constitute extemal information search is lacking. Past studies from the examination of extemal search for durable goods have included the number of informational sources frorn which information was sought, the amount and types of information soughk the time dimension over which infomztion was sought, the number of brands for which information was sought, and the manner in which the information was sought, as constituting extemal information search (Kiel & Layton, 198 1). In order to detemine which behaviours constitute external search, however. a consistent definition of what is meant by external search is required. For the purposes of this research. the general definition of extemal search used by Beatty & Smith (1987) will be employed: "External search is the degree of attention, perception. and effort directed toward obtaining environmental data or information related to the specific purchase under consideration" (Beatty & Smith. 1987. p. 85). Most studies on consumer information search have tended to focus on prepurchase events, with little. if any, emphasis given to information collected on an ongoing basis. It is proposed that an orientation focusing solely on pre-purchase search is deficient and unable to account for search activity that occurs without a recognized consumption need. More specifically, a study conducted by Bloch, Sherrell & Ridgway (1986) examined search activity outside of a purchase context. These researchers viewed the emphasis in the existing literature on pre-purchase information search as a conceptual shortcoming. and concluded that by limiting the study of search to prepurchase settings allowed only a subset of consumers' total search activity to be assessed. In their frarnework, search was conceptualized as involving two cornponents: pre-purchase search and ongoing search. It was hypothesized that consurners engaged in on-going search for two reasons: to build a useful bank of product information for future use, and for recreational activity. The results demonstrated that recreational motives were an effective predictor of the frequency of ongoing search engaged in and helped to explain a high proportion of the variance in search behaviour when combined with informational motives. The study also provided a strong relationship between a consumer's involvement in a product class and the propensity ro engage in ongoing search. This study is particuiarly useful in understanding situations where product information is obtained. yet the plan to purchase may be temporally removed, or in some cases. non- existent (Bloch, Shemll& Ridgway, 1986). To highlight the lack of attention paid to the activities undertaken after purchase, Hoyer argued that the traditional decision-making models (Engel, Kollat & Blackwell, 1973; Bettman; 1979) focus on the cognitive processing that occurs immediately prior to the act of purchase to the exclusion of other types of processing that may occur outside of the immediate choice context. While this theory (Hoyer, 1984) does not directly address the information search process per se, it has implications for those products that do not require a considerable degree of cognitive processing prior to purchase. These products, however, may require mote cognitive effort over repeated use of the product, rather than at the initial purchasing stage. This may occur in the case of a prescription dmg purchase due to side effects from taking the medication. curiosity, or educational efforts directed to the consumer via advertisements in the media or pamphlets provided in retail outlets. 2.4 Methodologies Used in the Information Search Literature Previous studies of consumer information search have employed different methods to obtain measures of extemal information search. The two methodologies most cornmonly employed in the literature are self-report, survey-based information, and those using a behavioural process methodology. Conflicting opinions in the literature, however, do not provide definitive answers as to which method of data collection is most appropriate. Studies conducted by Beatty & Smith ( 1987). Kiel & Layton ( 1981 ), Newman & Staelin (1972) have used self-reported responses to obtain measures of external information search. However. a problem associated with the retrospective studies of information seeking has been the low reliability and questionable validity of the measures used. Recall of the information search activities undertaken by consumers has been reported to be low (Newman & Lockeman, 1975). The study conducted by Newman & Lockeman (1975) compared survey-based and observation-based measures of information search. The results found little or no correlation between the observation-based and survey-based scores. The findings also suggest that consumen tend to undemport the arnount of in-store information search they engage in. The researchers raised concem over the accuracy of survey methods in accounting for the search undertaken by consumen, and they suggesr that better measures are needed to examine the extent to which various information sources are used by consumen. However, to support the use of survey-based methods. Beatty & Smith (1987) state that, "until a superior methodology appears. self-report measures seem to be the most reasonable measures of extemal search acûvity available for "real" purchase decisions" (p.93). Due to the inherent problems with self-reported measures of search. behavioural process methodologies using an information display board have been used to moniior extemal search (Moore and Lehmann; lacoby, Chestnut. Wei@& Fisher, 1976). This rnethodology employs a board that displays product information arranged in a brand-byattnbute matrix, and has allowed researchers to obtain more specific measures of search (lacoby et al.. 1976; Bmcks, 1985) However, the information display board methodology has some significant limitations. Most importantly, information display boards impose a well defined. comprehensive structure on what is often perceived to be an il1 structured problem. As well, information display boards also delirnit the size of the brand choice problem by defining the number of available alternatives and attributes (Brucks. 1985). Alternatives to retrospective self-report and behavioural process methodologies in the research have utilized direct observation of search activities, as well as verbal protocols from purchasers while they are shopping (Newman & Lockeman, 1975; Bettman, 1970). Direct observation is problematic, however, because the incidence of information seeking tends to be higher when consumers are being observed (Newman & Lockeman. 1975). Verbal protocols, on the other hand, are problematic because there is only a weak relationship between intended and actual information seeking (Lenz. 1984). III. METHODOLOGY 3.1 Research Purpose and Objectives The primary purposes of this study were: To identib segments of prescription dmg users by classiQing consumers according to similarîties on attitudinal dimensions related to health, prescription dmgs, and the conditions frorn which they suffer, if' attitude groups exist, to profile each segment in tems of demographic, situational and behavioural dimensions; If attitude groups exist, to suggest implications for various stakeholders, such as govemment agencies, health professionals, phamiaceutical manufacnirers. and retailers. Classifying prescription drug users into groups according to their similarity on attitudinal dimensions is useful for marketing practitioners. The technique is primarily descriptive in nature. No formalized hypotheses are required. Since the resulting groups or segments cannot be specified a priori, no hypotheses of the relationship between the groups (if they exist) and various demographic, situational and behavioural dimensions can be specified. 3.2 Research Design A survey research design was used. A self administered questionnaire was mailed to memben of a consumer mail panel who previously indicated that they had taken a prescription medication over the last 12 months. A mail questionnaire, using a consumer panel, was chosen for a variety of reasons: O Consumer panels are representative of the general population across many sociodemographic charactcristics; A sample representative of the population using a different methodology. such as through telephone interviewing. would be difficult and more expensive to obtain; Panel response rates are higher. with an average response rate of roughly 75% (Aaker & Day. 1983). Given that a large sample size was needed for this study, a mail panel provided greater assurance that a large sampie size would be achieved. in summary. a consumer mail panel provided a high response rate and a lower cost. though it is recognized that a trade-off may have been made in terms of the generalizability of the survey results to the Canadian prescription drug population as a whole. The survey was conducted using the Market Facts of Canada Ltd. Consumer Mail Panel. Questionnaires were sent to either the male or fernale head of household belonging to the Market Facts of Canada consumer panel. who in the 1995 Sumrner Flexibus conducted by Market Facts. indicated that they had taken a prescription medication over the last 12 months. The questionnaires were distributed to panel members early in the fa11 of 1995. 3.3 Questionnaire Development The questionnaire was developed using ideas obtained from the literature review, consultation with stakeholders in the phannaceutical industry, discussions with Market Facts of Canada Ltd., and the MSc. advisory committee. Questionnaire content was drawn extensively from past research conducted by Morris et al. (1987, 1992). Specific question areas drawn from this research related to the patient's experiences with the doctor and pharmacist in terms of receiving verbal and written information. the patient's question asking ability, the patient's use of other sources (other than the doctor and pharmacist) to obtain information, and 19 out of the 32 anjtudinal variables that were used as the basis of segmentation. The other attitudinal variables were borrowed h m propnetary studies supplied by representatives from the pharmaceutical indusûy. These variables were also used as part of the segmentation. The questionnaire was pretested with a sample of 20 graduate students. in addition to three relatives of the graduate student and advisory committee . The pre-test sample read through and completed the question critiquing question wording/comprehension. questionnaire flow, and survey length. The questionnaire was also reviewed by representatives of Market Facts of Canada Ltd. to ensure the language used was consistent with Company practices. 3.4 Statistical Analysis 3.4.1 Factor Analysis A factor analysis was conducted with a total of 32 different attitudinal items (24a- 24ff ;see Questionnaire in Appendix VTI) to identify psychographic dimensions which might underlie information search behaviour. The purpose of the analysis was to reduce the number of attitudinal items to a smaller number of dimensions which would be used as the basis for clustering. The data set was factor analyzed first by Rincipal Components Analysis and then by Principal Axis Factoring. This was done in accordance with Tabachnick and Fidell's (1989) recommendation of using PCA as the fust step in any factor analysis. which gives the researcher insight into the number and nature of factors. However, as Tabachnick & Fidell indicate. Principal Components Analysis is often not a sufficient factor analysis procedure because it analyzes al1 the variance in the observed variables. including error variance. Consequently, Principal Axis Factoring was used as the final bais for factor extraction. This method was deemed to be more suitable because it only analyzes the shared variance, and ignores variance due to error. This solution yielded the same number of factors as in the PCA analysis, and was interpretable. This solution was used to compute factor scores that could be used in the cluster analysis. Varimax rotation was used in order to increase the interpretability of the factors- It is an orthogonal method, used when the factors are expected to be uncorrelated. Varimax rotation was used in the factor procedure because there was no assumption made that the dimensions would be related to one another (Tabachnick & Fidell, 1989). The number of factors to be retained were determined using four guidelines: eigenvalues of the facton. the scrw test. the amount of variance accounted for by each factor and group of factors. and the interpretability of each factor. Fint, an examination of the eigenvalues was undertaken. Only factors having an eigenvaiue of one or more were considered since those with lesser values are not as important, from a variance perspective. as an observed variable (Tabachnick & Fidell. 1989). Second. the scree plot of the eigenvalues associated with each factor was examined empincally to detemine at which point there was a noticeable drop in the values from one factor to the next Most commonly. those facton with an eigenvalue of one or more are retained for further consideration. Third. the 5 factor through to 9 factor solutions were exarnined to determine the cumulative amount of variance for which each solution accounted. Those soiutions which had a significant increase in total variance explained from the previous solution were retained for further consideration. Fourth, within each solution. the factors were examined for their interpretability. The nature and meaning of each factor was judged according to the grouping of the original variables which were most highly associated with that factor. After a final factor solution was chosen, a decision was made regarding whether to use factor scores or composite variables as the basis for clustering. There were both advantages and disadvantages associated with each approach. Factor SCORS are advantageous because they take into account each of the item's reliability. which means that items receive different weights depending on their reliability. The drawback, however, is that the creation of factor scores capitalizes on chance relationships among variables so that factor-score estimates are biased (Tabachnick and Fidell, 1989). Tabachnick and Fidell also cite that factor scores suffer from indeterminacy because there is an infinite number of possible factor scores that can be denved, and that there is no definitive way to decide among them. Regarding the use of composite variables, they are best used when the scale is untested and exploratory, with little or no evidence of reliability or validity. The drawback to the use of composite variables is that each of the items that compose a factor may receive equd weight, despite the fact that their variance conûibutions may differ. Composite variables were used as the basis for ciustering due to their greater predictive ability, interpretability, and given that the scales were untested and exploratory. These composite variables were created using the variables which loaded highly on each of the factors from the Principal Axis Factoring method. The raw score values of al1 of the variables with loadings of .3 or more for a factor were totalled to produce a single composite variable or scale. Eight summated scales were created. These scales were reduced to a comrnon metric by averaging their total values by the number of variables that they were composed of. These averaged scales were used as input for the cluster analysis. 3.4.2 Cluster Analysis Cluster analysis was used to identify naturally occurring psychographic segments among the sample of prescription drug users. The segmentation was based on the eight attitudinal dimensions created through Principal Axis Factoring method and scale summation. The clustering method used was Ward's method. This clustering method uses a hierarchical method, and is considered to be one of the better clustering methods available (Hair, Anderson. Tatham & Black. i987). The advantage of a hierarchical method over a non-hierarchical method is that it does not require the specification of a starting seed which has to be specified based on a non-empirical critenon. Hair et al. (1987) state that the use of non-hierarchical techniques with random seed points is markedly inferior to hierarchical techniques. Ward's method starts the process of clustering by treating each case or respondent in the sample as a cluster. In each successive stage, one cluster is combined with one other cluster to which it is the closest. This process continues until at the last stage dl the cases have been combined into one large cluster. The agglomeration schedule output of this analysis summarizes what has occumd at each stage of the clustering process. The agglomeration schedule was used to judge the nurnber of clusters chosen. It presents which sub-chers are being combined at each particular stage and the distance between the most dissimilar points of those clusters. The stage at which a relatively large clustering coefficient appears indicates that two very different clusters are being combined. Following convention. the number of clusters chosen is the number associated with the stage immediately preceding the stage at which this large coefficient is noted. It seemed aso on able to expect that between 3 and 5 clusters would be identified among the sample of prescription drug users examined. Previous research had identified an average of about four types. With this in mind. the number of clusten to be accepted was detennined empirically by examining the agglomeration coefficients, assuciated with the different cluster solutions. Having chosen the number of clusters generated from the hierarchical model. the second step was to use a non-hierarchical procedure to confirm the results. Cluster means generated from the hierarchical method were input into the Quick Cluster method. a nonhierarchical method in order to confirm the results. In performing this type of cluster analysis, the initial seed points are the cluster centroids on the eight cluster variables. According to Hair et al. (1987). the advantages of the hierarchical rnethod are complemented by the ability of the non-hierarchical method to confinn the results by allowing the switching of cluster membership. If the non-hierarchical results agree with the results frorn the hierarchical approach, it provides support that it is a suitable cluster solution for the data set. 3.4.3 Cross-Tabulations Cross-tabulations are used to examine the relationship between two or more categorical variables. A chi-square statistic c m be used to test the nul1 hypothesis of no relationship between the two variables (Hair et al.. 1987). In this case. cross-tabulations were perfonned to determine if tespondent membenhip in a cluster was confmed by two reported behaviours. These variables were: asking a doctor to prescnbe a specific drug. and asking a pharmacist to dispense a generic drug over a brand name prescription medication. 3.4.4 Discriminant Analysis Discriminant analysis was used for each of three separate sets of predictor variables, demographics. situationai. and behavioural measures of information search. The goal of discriminant anaiysis was to find the dimension or dimensions dong which the cluster groupings differed and to find classification functions to predict group membership. Each discriminant analysis used the direct method. With the direct method, al1 predictors enter the equations at once and each predictor is assigned only the unique association it has with the groups (Tabachnick & Fidell, 1989). Other methods. such as hieranihical and step-wise methods were not used because there was no theoretical reason to suggest that certain variables should be entered into the equation prior to the entry of other variables. In order to determine the number of discriminant functions that best separate the cluster groupings. the eigenvalues. percents of variance, and canonical correlations were used to assess the significance of each discriminant function extracted. Following this. the plots of centroids were assessed to determine how the cluster groups were separated by the discriminant functions. The meaning of the functions are inferred from the pattern of correlations between the function and the predictors. Though consensus is lacking regarding how high correlations in a loading matrix must be in order to be interpreted. by convention. correlations in excess of .30 (9%of variance) may be considered eligible (Tabachnick & Fidell, 1989). Finally,classification functions were used to predict group mem bership and to check the adequacy of classifications for cases in the same sample through crossvalidation. Cross-validation involves dividing the sample randomly into two parts, and denving classification functions on one part, and testhg them on the other (Tabachnick & Fidell, 1989). The stability of the classification procedure was checked by crossvalidation. Approximately 25% of the cases were withheld from calculation of the classification functions. 3.4.5 Multinominal Logistic Regression A second approach used for undentandhg and predicting group membership was logistic regression. Logistic regression was used to identify the demographic variables that discnminated among cluster groups. This procedure allows for the examination of a dichotomous dependent variable and both continuous and categorical independent variables. According to Hair et al. (1987), logistic regression or logit analysis is preferred over discriminant analysis in certain circumstances because discriminant analysis relies on multivariate nonnality and equal variancecovariance matrices across groups. Logistic regression or logit analysis does not face these strict assumptions, thus making it a more appropriate technique when these assumptions are violated. Similarly. OGonnan & Woolson (1991) recommend using logistic regression for estimation when the underlying distribution is nonnomal since the estimates of the coefficients will be biased if discriminant analysis is used. In order to detemine the assessrnent of the fit of the model in logistic regression, the likelihood value (-2LL). which is sirnilar to R~ in multiple regression. was used. in interpreting the likelihood value, a weU fitting model should have a small value for -2LL. The model c m also be assessed by the classification table which compares actual events versus the predicted values. (Hair et al, 1987). 3.5 Research Assumptions First, subjects in the study were adults who had obtained at least one prescription medication for themselves in the past 12 months. It was assumed that respondents were able to recall relevant information that was received or sought about their prescription medication(s) or about the condition for which they suffer over the course of this tirnefiame; Second, it was assumed that the appropriate household member, who had responded to the screener questionnaire, completed the follow-up questionnaire: 3.6 Research Limitations The sample used in this research may not be representative of the Canadian prescription drug user population overall due to the fact that the sample was drawn from a defined population of panel members. which are self-selected rather than randomly selected. However, the fact that the demographic profile of this sample is sirnilar to the Canadian population of prescription dmgs users overall (See page 45 for more detail) suggests that the two groups are not widely divergent. An order bias, and consequently, an increase in response error may have occurred because of the consecutive arrangement of the thirty-two attitudinal scales from which the cluster solution was derived. Participants may have experienced response fatigue, which may have affected the answea they gave to the attitudinal items appearing at the end of the attitude battery. To mitigate the effects of orderbias, selected statements were worded in the negative to ensure that participants were reading and responding to the statements appropriately. IV. RESULTS 4.1 Introduction The research findings are presented in five main sections. The first section presents the response rate and composition of the sample. The second section presents the results of the factor analysis, which were used as the basis for conducting the cluster analysis. The third section presents the results of the cluster analysis, which sought to identify a typology of prescription drug users. The fourth section presents the findings of the cross-tabulations which were conducted in order to determine if the derived cluster membenhip could be confirmed by reported behaviours. Finally. the fifth section presents the fmdings of the discriminant and logishc regression analyses which sought to profile the resulting clusters in tems of demographic, situational and behavioural variables. 4.2 Sarnple 4.2.1 Response Rate A total of 600 questionnaires were sent to either the male or fernale head of household belonging to the Market Facts of Canada Consumer Mail Panel, who in the 1995 Summer Flexibus conducted by Market Facts, indicated that they had taken a prescription medication over the last 12 months. Of these, 456 prescription drug usen retumed completed questionnaires. This represents a response rate of approximately 7 6 2 -- consistent with similar studies of this nature. According to Aaker et al. (1983). consumer mai1 panels typically achieve an average response rate of 75% . 4.2.2 Sample Characteristics Roughly eighty percent of the sample were women (78%)and just under one-half of the sample were 55 years of age or older (45%). The largest proportion of the sample was represented by the elderly (28% were 65 years of age or older). Almost one-half of the sample had some education beyond high school. Nearly one-quarter (24%) of respondents were university educated. while another 18% had some other type of postsecondary education. The income level of approximately 60% of the sample was less than $60,000 per annum; 39% reported an annual household income of less than $30,000; 39% reported an income of between $30,000-$59,999 per year. Just under onequarter of the sarnple (224) eamed $60,000 or more on an annual basis. The sample was represented primarily by residents of Ontario (representing roughly 40% of the sarnple) and Quebec (24%). These provincial proportions are roughly equivalent to 1991 Census data population counts (i.e., Ontario 37%. Quebec 268). Two-thirds of the sample (67%) reported having filled a prescription medication within four weeks of receiving the questionnaire. Most of the sarnple received refills of an existing prescription medication (72%) cornpared to those who received a new prescription medication (28%). Three-quarters of the sample (758) were still taking the medication at the time they received the questionnaire; over one-half (53%) had been taking the medication for more than one year. Seventy percent (70%)of the sample reported that the prescription medication that they had filled most recently was for the treatment of a chronic illness, predominantly respiratory disease (i.e. asthma) (13%) and cardiovascular disease (i.e. hypertension) (19%). At the time of completing the questionnaire, onequarter (27%) of ihe sample reportcd that they were taking only one medication, 19% were taking two prescnption medications. 15% were taking three prescnption medications and 19% were taking more than three. This sarnpie is deerned to be representative of the population of prescnption drug users in ternis of age and gender because these characteristics are aligned with statistics given in the Annual Statistical Report of the Prescription Dnig Services Branch (19951996). This report cites that the highest percent of prescriptions used in 1995-1996 was in the 65 years or older group. receiving 44.1% of al1 prescriptions. By gender, females accounted for 60.8% of al1 prescriptions and received more prescriptions across al1 groups (beyond age 14) than males. Consequently, the sample is represented by the heaviest users of prescnption medications, and is therefore, appropriate for research into the information search activities of prescription drug users. 4.3 Factor Analysis The purpose of the factor analysis was to reduce the number of attitudinal items to a smaller set of dimensions. and to understand the underlying motivations of prescnption drug usen that may be related to information search behaviour. After removing univariate and multivariate outliers. a total of 433 cases were analyzed for the factor analysis procedure. The criterion given by Tabachnick & Fidell (1989) of having at least 5 cases per variable was achieved -- with approximateiy 13.5 cases per observed variable. Missing data was handled by rnean substitution in order to ensure an adequate sarnple size for analysis. Frequencies weR nin on the 32 variables and examined for skewness in their distributions. Though a few variables were skewed, factor solutions are useful even when observed variables are not normally distributed (Tabachnick & Fidell, 1989). To assess Iinearity. scatterplots were examined. Nonlinearity was not a concern, and therefore variable transformation was not considered necessary. Four different indicaton, generated through the factor procedure, were examined which confirrned that these attitudinal items were suitable for factoring. These included the correlation matrix, Bartlett's Test of Sphericity, the Kaiser-Meyer-Olkin measure of sampling adequacy, and the anti-image correlation matrix. Most of the correlations in the matrix were low (Appendix 1). Large sample sizes. however, tend to produce low correlations and since there were correlations of 0.3 and over. factor analysis may still be used (Tabachnick & Fidell. 1989). Bartleit's Test of Sphencity had a value of 345 1.7599 and a significance of less than 0.0001, though its sensitivity and dependence on sarnple size is likely to be significant given a large size even if correlations are low (Tabachnick & Fidell, 1989). The Kaiser-Meyer-Olkin measure of sarnpling adequacy had a value of 0.80416, indicating that the matrix is factorable. According to Tabachnick & Fidell (1989). values of .6 and above are required for good factor analysis. Further, most of the offdiagonal elements of the anti-image correlation matrix were low. This low proportion of large anti-image coefficients denotes that there are likely no correlations between the unique parts of the variables being factored. and therefore factor analysis may be used. To aid in the interpretation of the factor analysis, Principal Components Analysis was conducted to provide insight into the number and nature of factors. Using the accepted mle that factors with eigenvalues greater than one should be extracted (Tabachnick & Fidell. 1989). a nine factor solution was identified. These factors had eigenvalues of 5.14, 3.52. 2.15, 1.68. 1-46, 1.25. 1.19, 1-14, 1.O7 respectively. The underlying attitudes were labelled as Information Involvement. Self-Assured Knowledge. Doctor-Oriented Information. Information Avoidance, ManufacturerOriented Information, Self Care Orientation. Phamacist-Orientcd Information and Patient Decision Making. The identity of each the factors was infened from the group of attitudinal items loading the highest on that factor. A cut-off of -3 for inclusion of a variable in the interpretation of a factor was utilized. The item Ioadings for each factor are presented in Table 1. Based on the factor loadings. the ninth factor was deemed to be uninterpretable as only one item loaded highly on this factor. Other items loading on this factor just barely met the .3 cut-off for inclusion. Table 1: Principal Components Andysis Factor Solution 9.Rotated Factor Mavix Like-to know as much about my 0.68 medication... 24M Feel better about taking when knowledgeable... 24A Usually ask Dr. questions at tirne of medical 057 visit.. 241 Get information h m books and written ... 0.42 24DD Helpful if Dr.gave written information... OAS 24F Should be told about medication options... OR7 24FF Think of questions before medical OAl appointment... 24N Information is too hard for me to -0.05 understand... 24CC Dr. uses words 1don't understand... 0.06 24U Don't know enough to make informed -0.04 medication choices... 24EE Phanpacist is too far away to ask 0.09 questions... 24K Not cnough privacy at phannacy counter... 0.16 24J Don't think Drs. know enough about drugs... 0.13 0.10 24X Know more about my condition than orheS... 24L Know more about my medication than 0.24 ohers... 24Y Know where to find a11 the information 1 0.14 need ... 24AA Would.rather have Dr. make decisions than -0.09 to be given choice... 24V Aiways better t seek professional help than 030 to mat yourseik.. 24H Better to rely less on doctors and more on -0.05 your own common sense... 24BB Should be abIe to choose medication ... 0.15 24P No need to ask questions if trust doctor... -0.26 24B Helpfid to ask friends or family about 0.19 dnig ... 24s h g companies ought û~inform 0.15 consumers... 24D h g Company should tell me about cimg.,. 0.03 24E Doctor is open to questions ... 0.34 0.10 24R Doctor provides information about h g . . . 24C Phmacist provides info about the d m g ... 0.06 030 24G Usually ask pharmacist questions about dnig... 24T Want to be able to detemine if medication 032 1s working ... 242 Wmt info to decide if dnig should be 0.20 taken.. . 240 Rgmembering to take medication is -0.07 dtfficult... 24Q More concemed about my health than -0.04 othem... Loadings of .3and above are indicated in bord 0.27 0.09 -0.08 0.09 -0.09 0.21 0.20 0.01 0.23 0.46 -0.07 0.07 0.16 0.01 -0.0- -0.06 0 3 2 4.12 4.15 -0.02 4.26 0.18 -0.08 0.10 0.03 0.24 0.28 0.42 -0.04 0.01 0.14 0.07 4-19 0.03 -0.W 0.05 0.15 037 - 0 3 0.14 -0.21 -0.10 030 4.1 1 0.15 -0.03 0.00 0.75 -0.06 0.07 0.04 0.14 0.05 0.00 -0.23 0.64 43-15 -0.19 OS5 -0.09 0.10 -0.15 0.01 -0.05 0.26 -0.01 -0.06 0.14 0.17 0.14 0.07 0.27 036 -0.19 0 3 0.29 -0.46 0.23 0.16 -030 0.24 0.78 0.03 0.01 0.02 0.09 -052 -0.02 0.19 0.02 4.01 -0.12 -0.07 0.23 0.05 0.41 0.21 0.05 0.28 0.15 0.07 0.06 0.19 -0.E 0.75 4.10 -0.03 -0.01 0.24 0.04 0.06 0.00 0.61 031 -0.28 0.03 4.05 0.34 0.44 0.14 -0.42 0.06 -030 -0.M -0.02 0.12 0.06 -0.64 0.08 -0.08 O. L 7 0.14 -0.00 0.07 0.01 0.60 -0.05 4.09 0.03 0.48 0.44) 0.03 0.12 0.25 0.02 035 -0.07 0.66 -0.05 -0.03 -0.19 -0.15 -0.16 0.06 0.29 059 0.10 -0.08 -0.OC 0.09 0.01 -0.01 0.79 0.10 0.05 0.15 0.14 0.05 4.13 -0.03 0.79 0.65 -0.16 0.03 0.70 4.12 -0.16 0.17 -0.05 0.02 -0.03 0.04 O.I Z O.12 -0.02 0.05 0.05 -0.16 -0.02 0.02 0.19 O. 18 0.00 -0.00 0.12 0.02 O.1 O 0.02 -0.11 4.05 0.1 7 0.14 0.10 -0.04 0.14 -0.00 -0.08 0.12 -0.01 0.08 0.77 0.00 0.06 0.71 -0.03 0.10 0.08 -0.08 0.09 039 4.08 O.1 1 0.23 4.00 0.12 0.29 0.19 -0.02 057 0.24 -0.09 -0.03 0.03 -0.01 0.05 0.07 0.08 0.79 0.42 0.12 0.08 0.23 0.46 031 -0.14 0.04 0.47 -0.02 Table 2 presents the attitudinal items that make up each factor with their suggested factor narnes. 'able 2: S u w t e d N a m s For Principal Components Anaiysis Factoring Method Results Que. # Factor 1: 24W+ 24M+ 24A+ 24DD+ 24F+ 241+ 24FF+ 24V+ 24E+ 24G+ 24T+ Factor 2: 24X+ 24L+ 24Y+ 24Q+ 241+ Factor 3: 24R+ 24E+ 24P+ 24A+ 24K24124Y+ 24AA+ Intormatlon Involvement 1 like to know as much as 1 can about the medication the doctor prescribes for me. 1 feel better taking drugs when 1 am knowledgeablc about them. 1 usually ask the doctor questions about the cimg prescribed at the time of my medical visit. It would be helpful if the dcctor provided wntten information about the drug he/she prescribes. When there is more than one medication to treat rny condition. 1 should be told about each one. 1 often like to get information about my medication from books and other written materials. t some questions and wrote them down It would be easier to ask the doctor questions if 1 ~ o u g hof before my appointment. It's always bener to seek professional help than to try to m a t yourself My doctor is generally open to questions about the dmg(s) he or she prescribes 1 usually ask the phmacist questions about the dru@) when 1 am having the prescription filled 1 want infornation about prescription drug(s) so 1 can determine if the medication is working or not. Seif-Assured Knowledge 1 feel 1 know more about my condition than do other people experiencing the sarne heaith condition as me. 1 feel 1 know more about my medication than do other people who take the sarne medication as me 1 feel I know where to find al1 the information 1 need on my medication. I feel 1 am more concerned about my health than are otfier people my age. 1 often like to get information about my rnedication(s) from books and other written materials. Doctor-Oriented Information The doctor always provides me with information about the medication he or she prescribes for me. My doctor is generally open to questions about the drugs he or she prescribes. There is no need to ask questions about prescription dmgs if you m s t your doctor. 1 usually ask the doctor questions about the drug prescribed at the time of my medical visit. There is not enough privacy at the pharmacy counter to ask questions about the medication 1 have been prescribed. 1 don't think doctors know enough about the drugs they prescribe 1 feel 1 know where [O find al1 the information 1 need on my medication 1 would rather have the doctor make the decision about my treatrnent than for him or her to give me a whole lot of choices. Factor 4: 24N+ 24CC+ 24U+ 24AA+ 24P+ 24EE+ Factor 5: 24!3+ 24D+ 24T+ 24DD-t Factor 6: 24V24H+ 24B+ 24AA- 24I+ 243+ 24BB+ Factor 7: 24C+ 24G+ 24EE- Idormation Avoidanœ Information about rny medication is too hard for me to undentand. The doctor uses words 1 don't understand when tefling me about the drug hetshe is prescribing. 1 feel 1 don't know enough about my medication to make informed choices about which medication 1 should take. 1 would raiher have the doctor make ihe decision about my mament than for him or her to give me a whole lot of choices. There is no need to ask questions about prescription dmgs if you trust the doctor. The pharmacist is too far away behind the pharmacy counter for me to ask questions about the drug(s) prescribed Manufacturer-OrientedInformation Drug cornpanies ought to inform consumers about health issues and medications. The cornpany who makes the drug should tell me what i need to know about my medication. 1 want information about my prescription dmg(s) so 1 can detemine if the medication is workhg or not it would be helpful if the doctor provi&d writren information about the drug(s) helshe prescribes. Seit-CareOrientation It's dways better to seek professional help than to try to ueat yowself. It is better to rely less on doctors and more on your own cornmon sense when it comes to carhg for your body. It is helpful to ask my fnends or family questions about the drugs 1 am taking. 1 would rather have the doctor make the decision about my treatment than for him or her to give me a whole lot of choices. 1 often Iike to get information about my rnedication(s) From books and other written matenals. 1 don't think doctors know enough about the drugs they prescribe. When there is more than one medication to treat my condition. 1should be allowed to choose which medication I want to cake. Pharmacist-Oriented Infornation The phmacist always provides me with infornation about the medication he or she gives me. 1 usually ask the pharmacist questions about the drugs when I am having the prescription fillesi The pharmacist is too far away behind the counter for me to ask questions about the h g prescribed. Factor 8: Patient Decision Making 24BB+ When there is more than one medication to mat my condition. 1 should be allowed to choose which medication 1 want to take. 1 want information about my prescription h g so 1 can decide if 1 should take the medication. 1 feel 1am more concemed about my health than are other people my age. 1 want information about rny prescription drug so 1can determine if the medication is working or not. When there is more than one medication to treat my condition. I should be iold about e x h one. 1 would rather have the doctor make the decision about my marnent han for him or her to give me a whole lot of choices 24Z+ 24Q+ 24T+ 24F+ 24AA- Factor 9: 224Tc Incondosive 24F24FF+ When there is more than one medication to ueat my condition. 1 should be told about each one. It would be easier to ask the doctor questions if 1 thought o f some questions and wrote hem down before my appointment Remernbering to take my medication is often difficult for me. I want information about prescription dmg(s) so 1 can determine if the medication is working or not The PCA solution was used to provide guidance into the number and nature of the factors. However, it was not chosen because this method analyses al1 the variance in the observed variables, including error variance. A Principal Axis Factoring was used as the final b a i s for factor extraction. This method was deemed to be rnost suitable because it only analyzes the shared variance, and eliminates variance due to error (Tabachnick & Fidell, 1989). This solution yielded the sarne nurnber of factors as in the PCA analysis, and was interpretable. An eight factor solution was most interpretable. and as a result, was selected from the Principal Axis Factoring results to represent the psychographic dimensions which might underlie information search behaviour. In addition. compared to the nine factor solution, which emerged for both PCA and PAF procedures. the eight factor solution accounted for 40.4% of the variance, compared to 42.28 of the variance in the nine factor solution. Four out of the eight factors generated had eigenvalues greater than one. The comsponding eigenvalues for each of the factors were as follows: 4.62.2.94. 1.56, 1.13. .86, .67, .64. .52 respectively. Though eigenvalues of less than one represent less variance than a single observed variable (Tabachnick & Fidell, 1989). the remaining 4 out of the eight factors were retained because they were consistent with the results obtained through the Principal Components factoring method, and were interpretable. The underlying attitudes were labelled as Information Involvement. Self-Assured Knowledge, SelfCare Orientation. Information Avoidance, Manufacturer-ûriented Information. Doctor-Oriented Information, Pharmacist-Onented Information, and Patient Decision Making. The identity of each the factors was inferred from the group of attitudinal items loading the highest on that factor. A cut-off of .3 for inclusion of a variable in the inierpretation of a factor was utilized. The item loadings for each factor are presented in Table 3. - able 3: Principal Axis Factor Solution 8 Factor Solution Rotated Factor Matrix m l k e to know as much about my rnedicauon... 24M Feel better about taking when knowledgeable... 24A Usually ask Dr. questions at tirne of rnedical visit... 241 Get information from books and written... !4DDHelpful if Dr.gave wriuen information... 24F Should be told about medication options... Z4FF Think of questions before medical appointment.. 24N Information is too hard for me to understand... Z4CCDr. uses words 1 don't understand.. 24U Doq't know enough to make informed medication choces... 14EEPhaxmacist is t w far away to ask questions... 24K Not enough privacy at pharmacy counter... 241 Don? think Drs. know enough about dmgs... 24X Know more about my condition than others... 24L Know more about my medication than others... 24Y Know where to find ail the information 1 need... !4AAWould ra@erhave Dr. make decisions than to be given choice... 24V Always bener to seek professional help than to treat yourself. .. 24H Better to rely Iess on doctors and more on your own common sense... !4BBShould be able to choose medication... 24P No need to ask questions if trust doctor... 24B Helphl to ask friends or family about drug ... 245 h g companies ought to inform consumers... 24D Drug Company should tell me about drug... 24E Doctor is open to questions... 24R Doctor pmvides information about drug... 24C Pharmacist provides info about the drug ... 24G Usually ask pharmacist questions about drug... 24T Wantto be able to determine if medicarion is working... 242 Want info to decide if dmg should be taken... 240 Remernbering to take medication is dificult... 244 More concemed about rny health than others... Factor Factor tactor Factor Factor Factor Factor Facto] 1 2 3 4 5 6 7 8 65 -.[O -26 -.O2 -10 .18 .19 -20 Table 4 presents the attitudinal items that make up each factor with their suggested factor narnes. *able 4: Suggested Factor Names For Principal Axis Factoring Method Resdts Facfor 1: Inionnation Involvement 24W+ 24M+ 24A+ 24DD+ 241+ 24F+ 24T+ Factor 2: 24N+ 24CC+ 24U+ 1 like to know as much as 1 can about the medication the doctor prescribes for me. 1 feel bener taking drugs when 1 am knowledgeable about them. 1 usually ask the docmr questions about the drug prescribed at the time of my medical visitIt would be helphd if the doctor provided written information about the drug helshe prescribes. 1 often Iike to get information about my medication from books and other written materids. When there is more than one medication to treat my condition. 1 should be toId about each one. 1want information about my prescription drug so 1can determine if the medication is working or not 24J+ Information Avoiâance Information about my medication is too hard for me to understand. The doctor uses words I don't understand when telling me about the drug he/she is prescribing. 1 feel I don't know enough about my medication to make infomed choices about which medication 1 should take. The phannacist is too far away behind the counter for me to ask questions about the drug(s) helshe prescribes. There is not enough pnvacy at the pharrnacy counter for me to ask questions about the medication 1 have been prescribed. 1 don't think doctors know enough about the drugs they prescribe. Factor 3: 24X+ SeK- Assured Knowledge 1 feel1 know more about my condition than do oiher people experiencing the same health condition as 24L+ 24Y+ me. 1 feel 1 know more about my medication than do other people who take the same medication as me. 1 feel 1 know where to find al1 the information 1 need on my medication. 24EE+ 24K+ Factor 4: 24A.A24V24H+ 24B+ 241+ 24J+ 24BB+ 24P- Self-Care Orientation 1 would rather have the doctor make the decision about my maunent than for him or her to give me a whole lot of choices. It's always better to seek professional help than m uy to m a t yourself. It is better to rely less on doctors and more on your own common sense when it cornes to caring for your body. It is helpful to ask my fnends or farnily questions about the dmgs 1 am taking. 1 often like to get information about my medication(s) from books and other wrinen rnaterials. I don? think doctors know enough about the h g s they prescribe. When there is more than one medication to mat my condition. 1 should be allowed to choose which medication 1 want to take. There is no need to ask questions about prescription drugs if you trust the doctor. Factor 5: 24S+ 24D-t 24DPc 24T+ Manufacturer-OrientedInformatioa g cumpanies ought to inform consumers about health issues and rnedications. The company who makes the h g should tell me what I need to know about my medication. It would be helphl if the doctor provided written information about the dmgs helshe prescribes. 1 want information about my prescription dnig so 1 can determine if the medication is worlcing or not Factor 6: 24E+ 24R+ 24A+ Doctor-Oriented I n f o ~ t i o n My doctor is generally open to questions about the dnigs he or she prescnbes. The doctor aiways provides me with information about the medication he or she prescribes for me. [ usuaily ask the doctor questions about the dnig prescribed at the tirne of my medicd visit. Factor 7: 24C+ 24G+ 24EE- Pharmacist-ChienteciInformation Factor 8: 242+ 24T+ 24BB+ h The phmacist dways provides me with information about the medication he or she gives me. I usually ask the pharmacist questions about the drugs when 1 am having the prescription filIed. The pharmacist is too far away behind the counter for me to ask questions about the dmg prescribed. Patient Decision Making 1 want information about my prescription dmg so [ can decide if 1 should take the medication. 1 want information about my prescription h g so 1 can detemine if the medication is working or not When there is more than one medication to m a t my condition. 1 should be allowed to choose which medication 1 want to take. After reviewing which variables loaded highly on each of the factors, composite variables were created by surnming the items with loadings of .3 or more, and averaging the score over the total number of variables in the equation. Composite variables were used as the b a i s for clustering because of their predictive ability and interpretability. Hair et al. (1987) suggest that when the scde is untested and exploratory, with little or no evidence of reliability or validity. composite variables should probably be used. The reliability procedure indicated that almost al1 of the items included in the scale were reliable measures of each of the underlying anitudinal dimensions (Table 5). Though Murphy & Davidshofer (1994) cite that there is considerable variability in reported levels of reliability, estimates of 0.7 and over are deemed to be acceptable for iating scales. Reiiability estirnates lower than 0.60 are usually thought to indicate low levels of reiiability (Murphy & Davidshofer. 1994). It is important to note. however. that reliability estimates are denved as a function of the number of items. and the average interconelations among those items. Only Scale-7, the scaie related to information from the pharmacist, fell below the 0.6 reliability coefficient critenon. This item, however, consisted of only three variables. which may contribute to its comparativeiy lower reliability level. Al1 eight scdes were used as the basis for the clustering procedure. Table 5: Reüability Coeflicients for Composite Variables Standardized Item Alpha 4.4 Scale-1 Scale-2 Scale-3 Scale-4 Scde-5 Scale-6 Scale-7 Scale-8 -7431 .63U .7099 .6705 .67 13 .7 172 5487 .fi464 Cluster Analysis Reliminary cluster analysis, using Ward's method, indicated that there were likely three distinct groups of prescription drug users. The agglomeration schedule produced was visually inspected. Appendix III presents the last seven stages of the agglomeration schedule. Table 6 presents the agglomeration coefficient for the first 1 through 7 cluster groupings. Following convention, the nurnber of clusters to be chosen is the number associated with the stage immediately preceding the stage at which a significant drop in this coefficient is noted. Since the largest drop was seen in going from three to four clusters, the three-cluster solution was selected. Tabie 6: Analysis of Aplomeration Coeflicient for Hierarehicai Cluster Analysis Number of Clusten Percentage Change in Agglomeration Coeffiaent to Next Level Al1 the prescription d m g users were then classified according to the similarity of their scores on each of the underlying attitudinal dimensions. The three segments were narned according to their score on each of the attitudinal dimensions (Table 7). Together. these scores indicate the nature of the patterns of attitudes about each of the three consumer segments. 1 Cluster Groups 1 Confident Decision Maken (N=433) 1 Uninformed (N=131: 30%) Scale-l=Infomation Involvement; Scale-Z=Information Avoidance; Scde-3=Self-Assured Knowledge: Scale_4=Self Care Orientation: Scale-S=Manufacturer-Oriented Information; Scale-6=Doctor-Onented Information: Scale-7=Pharmacist-Oi7ented Infornation; Scale-8=Patient Decision Making. The next step was to use a non-hierarchical procedure to confirm the results. Cluster means generated from the hierarchical method were input into the Quick Cluster method, a non-hierarchical method in order to confinn the ~ s u l t s .In performing this type of cluster andysis, the initial seed points are the cluster centroids for each of the eight variables as determined from the hierarchical procedure. As part of the non-hierarchicd results from the Quick Cluster approach is an analysis of variance which tests the effects of the attitudinal dimensions upon cluster membership (Table 8). In this case, the analysis indicated that the effects of each of the attitudinal dimensions on group membership were significant. This meant that the differences between the three segments, on each of the amtudinal dimensions, were likely not due to chance. Table 8: Results of Non-hierarchicalCluster Analysis with initial Seed Points fmrn merarchical aesults Cluster Scale-1 Scale-2 Scale-3 Scale-4 Scale-5 Scale-6 Scale-7 Scale-8 Cluster Size Classification cluster centres r 1 1 5.6 3.83 3.73 3.90 5.65 5.17 4.14 5.1 O t 33 2 6.3 3.O4 532 4.44 6.O3 6.14 5.92 5-99 166 3 5.04 2.5 1 3.9 1 3.17 4.1 1 6.09 5.44 3.27 131 Finai cluster centres Variable Cluster M.S. E m r M.S. F Ratio Scale- 1 75.4239 .546 I38.0439 Scale-2 74.8729 399 83-2752 Scale-3 134.4076 1 570 85.6034 Scale-4 69.0083 -797 86.4849 Scale-S 154.1052 .969 159.OO36 ScaIe-6 80.0545 1 .O50 76.192 1 Scale-7 1 145909 1 -273 90.0 151 Scale-8 276.7452 1.014 772.8252 The mean scores the clusters had on al1 of the variables input into the cluster analysis are presented in Table 9. 'able 9: Mean Scores on Attitudinal Variables Used in Clusi Information InvoIvement 24W+ 1 like to know as much as I can about the medication the doctor prescribes for me. 1 feel better taking h g s when 1 am knowledgeable about 24M+ them. 24A+ 1 usually ask the doctor questions about the h g prescnbed at the tirne of my medical visit. 24DDI It would be helpful if the doctor provided written information about the dmg hdshe prescribes. 1often like to get information about my medication h m 24I+ books and other M n e n materials. When there is more than one medication to mat my 24F+ condition, 1 should be told about each one. 24T+ 1 want information about my prescription h g so 1 can determine if the medication is working or not Information Avoidance 24N+ 24CC+ 24U+ 24EE+ 24K+ 243+ Information about my medication is too hard for me to understand. The doctor uses words 1 don't understand when telling me about the drug helshe is prescribing. 1 feel 1 don't know enough about my medication to make informed choices about which medication 1 should taJce, The pharmacist is too far away behind the counter for me to ask questions about the dmg(s) helshe prescribes. There is not enough privacy at the phannacy counter for me KI ask questions about the medication 1 have been prescnbed. 1 don't think doctors know enough about the dmgs they prescri bc. Self-kured Knowledge 24X+ 24L+ 24Y+ 1 feel 1 know more about my condition than do other people expexiencing the same heaith condition as me. 1 feel 1 know more about my medication [han do other people who cake the same medication as me. 1 feel 1 know where to find ail the information 1 need on my medication. SeK-Cam OrientaLion 24AA- 24V24H+ 248+ 24I+ 1 wouId rather have the doctor make the decision about my matment than for him or her to give me a whole lot of choices. It's always better to seek professional help than to try to mat yourself. It is bener to rely less on doctors and more on your own rommon sense when it cornes to caring for your body. It is helpfui to ask my friends or family questions about the dmgs 1 am taking 1 often like to get infonnation about rny medication(s) from books and other written materials. Self-Glue Orientation (cont'd) 24J+ 1 don't think doctors know enough about the dmgs they prescribe. 24BB+ When there is more than one medication to treat my condition, 1 should be allowed to choose which medication 1 want to take. 24PThere is no need to ask questions about pmcription h g if you trust the doctor. ManufacturerOriented Information 24S+ h g companies ought to infom consumers about hedth issues and medications. 24ib The Company who makes the dmg shouId tell me what 1 need to know about my medication. 2 4 D b It would be helpful if the doctor provided written information about the dmgs hdshe prescribes. 24T+ 1 want information about my prescription h g so 1 can detemine if the medication is working or not. Doctor-Orienteci information 24E+ My docior is generally open to questions about the dmgs he or she prescribes. 24R+ The doctor always provides me with infoxmation about the medication he or she prescribes for me. 24A+ 1 usually ask the doctor questions about the dmg prescribed at the time of my medical visit. Pbarmacist-Orienteô information The p h m a c i s t always provides me with information about the medication he or she gives me 24G-e 1 usually ask the phamacist questions about the dmgs when I am having the prescription filled. 24EEThe pharmacist is too far away behind the counter for me IO ask questions about the dmg prescribed. Patient ûecision Making 24C+ 242+ 24T+ 24BB+ 1 want information about rny prescription dnig so 1 can decide if 1 should take the medication. 1 want information about rny prescription dnig so 1 cm detemine if the medication is working or not When there is more than one medication to treat my condition. I should be allowed IOchoose which medication 1 want to take. A description of the three cluster segments is presented below: 4.4.1 System Skeptics This group was composed of 133 prescription drug users or approxirnately 3 1% of the sample. Consumers in Cluster #1 (System Skeptics) tended to exhibit a higher level of information avoidance than those in the other two clusters. They tended to perceive barriers to receiving information from health professionals. and lacked confidence in their ability to make informed health care decisions. They were most likely to feeI the information was too hard for them to understand, to claim that doctors used words they didn't understand, or that pharmacists were too far away to ask questions about the drugs they had been prescribed (Table 9). In addition, the System Skeptics tended to be less positive about the role of doctors and pharmacists in educating patients about medications compared to the other two clusters. They were the least likely to feel that both docton and pharmacists provided them with information about their medication. and they were the least likely to ask questions about their medication of these professionals. 4.4.2 Confident Decision Makers This group was composed of 166 prescription drug users or approximately 38% of the sample. Consumers in Cluster #2 (Confident Decision Makers) tended to be more proactive when it came to decisions about their health. They tended to want to know as much as they could about their rnedications and felt more cornfortable taking their rnedications when they were knowledgeable. They also tended to be confident in what they knew. They were more likely to perceive themselves to be more knowledgeable about their medication and health compared to the rest of the population. Confident Decision Makers appeared to be more empowered when it came to decisions about their health. They tended to want to take the responsibility on thernselves. radier than have someone else make the decisions for them. They were more likely to find ii helpful to ask their fiiends and family questions about their medications, and liked to read books and other written materials to get as much infonnation as they could. They also appeared to be receptive to information from a variety of infonnation sources -- d i ~ c t l yfrom the manufacturer, as well as from traditional sources, like doctors and pharmacists. Most irnportantly, they more often wanted to have the final Say; they wanted to decide whether they should take the medication, to determine whether ir was working or not, and to decide which medication they should take among the available alternatives. 4.4.3 Uninformed Followers This group was composed of 131 prescription drug usea or approximately 30% of the sample. Consumers in Cluster #3 (Uninformed Followers) did not perceive barriers to receiving information about medications and their health, nor did they want to bear the responsibility of making medication decisions themselves. They were the most likely to feel that it was better to seek professional help than to try to treat themselves. and felt that there was no need to ask questions if you ûusted your doctor. This group of consumers was most confident in placing this in the hands of traditional healthcare providers docton, and to a lesser extent. pharmacists. They appeared to be less interested in receiving any infonnation directly from drug manufacturers. 4.5 Cross Tabulations Cross-tabulations were performed to determine if respondent membership in a cluster was supported by each of two reported behaviours. The variables used were related to the propensity to ask a doctor to prescnbe a specific dmg, a s well as to ask a pharmacist to dispense a generic dmg over a brand name prescription medication. The results indicate that the Confident Decision Makers (5 1%) were more likely to ask a doctor to prescnbe a specific medication over System Skeptics (37%) and Uninformed Followers (40%), which is consistent with their propensity to be involved in decisions related to their health. Table I O presents the results from this cross tabulation. The chi-square was statistically significant, with a value of 7.18. 2 df and a significance level of .O3 Table 10: Ever Asked Doctor to Prescribe Specific Medication System Skeptics Confident Decision Makers Uninfomed Followers Row Toul 1 Yes No Count Row Pct Col PCC Total Pct 49 26.3 36.8 11.4 85 45.7 51.2 19.8 52 28 .O 39.7 12.1 Count Row Pct Col Pct Total Pct 84 34.4 19.5 81 33.2 48.8 18.8 79 32.4 603 18.4 133 30.9 166 38.6 30.5 Column Total 63.2 131 186 13.3 234 56.7 430 100.0 Consistent with their greater likelihood of asking a doctor to prescnbe a specific medication, the results also indicated that Confident Decision Makers (59%) were more likely to ask a pharmacist to dispense a genenc medication than System Skeptics (43%) and Uninformed Followers (43%). Table 1 ï presents the results from this cross tabulation. The chi-square was statistically significant. with a value of 10.59, 2 df and a significance level of .01. Table 11: Ever Asked Pharmacist For Ceneric Substitution Yes No Systern Skeptics Confident ûecision Makers Uninformed Followers Count Row Pct Col Pct Total Pct 56 26.7 42.7 13.1 97 46.2 59.1 22.7 57 27.1 33.2 13.3 Count Row Pct Col Pct Total Pct 75 34.6 573 17.6 67 30.9 40.9 15.7 34.6 56.8 17.6 2 17 50.8 Column Toial 30.7 131 1 64 38.4 132 30.9 427 100.0 75 Row Total 2 IO 49.2 The differences among the groups are statistically significant and in the expected direction (e.g., a Confident Decision Maker is more likely to ask for a generic drug than an Uninfomed Follower), but these differences are not as large as might be expected. However, since the self-reported behavioural data supports the attitudinal data (i.e.. Confident Decision Makers are more likely to be deciding on their medication), the attitudinal data has at least some validity. 4.6 Discriminant Analysis Overail, the results from the three discriminant analyses indicated that thex were significant differences across the cluster groups in tems of their reported information search behaviour. demographics, and characteristics d a t e d to their health. 4.6.1 Behaviourai Measures as Predictors The 12 behavioural measures used in the discriminant procedure were as follows: 1. 2. 3. 4. 5. 6. 7. 8. 9. 1O. II. 12. counselled by pharmacist about drug; counselled by doctor about drug; counselled by doctor about condition; counselled by phamacist about condition; asked questions of pharmacist about condition; asked questions of doctor about condition; number of sources used for information about condition; searched for information on condition; number of sources used for information about dmg; asked questions of pharmacist about drug; asked questions of doctor about drug; searched for information on dmg. For the first discriminant procedure which used behavioural measures to predict group membership, two discriminant functions were calculated, with a combined x2(24)=87.28,p c.01. After rcrnoval of the first function, there was still a strong association between groups and predictors, x2(11)=28.39, p c.01. The two discriminant function accounted for 68% and 3296, respectively, of the between-group variability (Table 12). Table 12: Canonical Discriminant Functions For Behavioural Variables Chi-Square Function Pe-nt of CurnuIative Wilks' Vanance Percentof Lambda Variance df Signi ficance Level 1 68.3 1 68.3 1 0.8 1 87.28 24 .O0 2 3 1.69 100.00 0.93 28.39 1I -00 Examination of the group centroids shows the first discriminant function rnaximally separates Cluster 1, the System Skeptics. from the other two cluster groups. The second discriminant function discriminates cluster 3, the Uninforrned Followers, fiom cluster group 1 and group 2. Table 13: Canonical Discriminant Functions Evaluated At Croup Means Cluster Croups Function 1 Fwiction 2 I -56624 .O805 1 The loading ma& of correlations between predictors and discriminant hnctions, as shown in Table 14, suggests that the best predictors for distinguishing between cluster 1, the System Skeptics and the other two groups (first function) are counselling activities conducted by the phannacist about the drug (COUNLPH)and about the condition (CNSLPHCN),and counselling activities by the doctor about the dmg (COUNSLDR) and condition (CNSLDRCN).Cluster 1, the System Skeptics are less Iikely to report that they were counselled by their phannacist about the drug they were prescribed (mean=3.12) than Confident Decision Makers (mean=5.54) or Uninformed Followers (mean=5.06), as well as their doctor (mean=4.37) versus Confident Decision Makers (mean=5.55) and Uninformed Followers (mean=5.77). They are also Iess likely to report being counselled by their phannacist (mean=. 16) or doctor (mean= 1.83) about the condition for which they are being treated. (Table 15). Table 14: Results of Discriminant Function Analysis of Information Search Behav Univariate Correlations of predictor variables F(2.409 ) with discyiminant functtons Predictor Variables 1 2 Counselled b Pharmacist abouibu (COUNLP~) 91 -.M 26.6530 Counselled bv Doctor about DiIl (coUNSL&> 55 -.29 10.9716 1 1 1 Counselled by Doctor about Condition (CNSLDRCN) 1 Counselled by Pharmacist about Condition (CNSLPHCNI Asked Pharmacist about Condition (ASKPHCN) -15 -16 1.0633 Asked Doctor about Condition (ASKDRCN) -.I7 .O 1 -9507 No. of.Sources Used for Information about Condition (SRCHCON#) .15 .62 63755 Searched for Information on Condition (SRCHCOND) -14 .60 5.9682 No. of Sources Used for Information about Drug (ANYINF#) .19 .45 4.1859 - .O2 36 4.6298 -1 I 38 2.5403 Asked Phmacist about h (QUESTPH 1 Searched for Information about Dru ~YINF& ~ s k e dDoctorabout h g (QUESTDR) g 1 -.O8 ( -46 1 3.3248 Table 15: Croup Meam by Predictor Variables. Cluster Groupings Predictor Variables 1 2 3 Counselled b Pharmacist abou<L 3.12 554 5 .O6 Counselled by Doctor about Dru (coUNSL~~) 4.37 555 5.77 Counselled b y J?octor about Conditton (CNSLDRCN) 1.83 2.4 1 2.43 Counselled b y P m a c i s t about Condition (CNSLPHCN) -16 -50 -44 No. of.Sources Used for Information about Conhtion (SRCHCON#) -73 -97 .54 Searched for .formation on Condition -40 -5 1 .3 1 No. of Sources Used for Information about Drug (ANYIM;#) -62 .86 -55 Asked Pharmacist about Dnrg 50 .56 27 Searched for Information about 39 -47 .34 .74 .74 -44 (COUNLPA) L 4 (SRCHCOND) (QIIESTPH) ~~0~ L Asked Doctor about Drug (QUESmR) r On the second discriminant function. which separates cluster 3, the Uninfomed Followers from cluster 1 and 2. predictors related to information search behaviour. such as whether or not search was conducted for either the drug prescnbed or the condition being treated (ANYINFO: SRCHCOND.respectively), as well as the number of sources sought for information were the best predictors for distinguishing between Cluster 3 venus the other two groups (ANYINF#; SRCHCON#, respectively). As shown in Table 15, the Uninfomed Followen were less likely to search for information about the condition for which they were being treated (mean = . 3 l ) than Systern Skeptics (mean = -40)and Confident Decision Makers (mean = -5 1). and cited fewer sources when they conducted information search about their condition (mean = 254) than the other two groups (mean = .73; mean = .97. respectively). This group is also less iikely to engage in search for information about the dmg they were prescribed (mean=.34) than System Skeptics (mean = .39) and Confident Decision Makers (mean = .47), and cited fewer sources when they conducted information search about the drug (mean = -55vs. Cluster 1=.62 and Cluster 2=.86). Cluster 3, the Uninformed Followers were also less likely to ask questions of their pharmacist (QUESTPH) (mean=.27) or doctor about the dmg they were prescribed (QUESTDR) (mean=.44) than the other two ciusters (mean=.50; mean = .56 respectively for pharrnacist; mean=.74; mean=.74 respectively for doctor). The classification results indicate that a total of 52.2% of the cases were correctly classified, compared to 37.6 % that would be correctly classified if al1 respondents belonged to the largest cluster grouping, or 33.6% with a classification accuracy achieved by random or chance grouping. Table 16: Classification Results for Behavioural Predictors Actual Groups Group Predicted Croup Membership No. of Cases 1 2 3 I 131 71 54.2% 37 28.28 1 7.6% 2 155 34 21.9% 89 57.4% 32 20.6% 3 126 27 21.4% 44 34.9% 55 43.7% 23 1 Percent of "grouped"cases comcctly classified: 52.18% The stability of the classification procedure was checked by a cross-validation mn. Approximately 25% of the cases were withheld from calculation of the classification functions. For the 75% of the cases from whom the ~Iassificationswere derived, there was a 52.4%correct classification rate. For the cross-validation cases, 42.4%were correctly classified, compared to 33.6% that would be achieved by chance or random grouping. Table 17: Classification Results for Cases Selectec for Use in the Analysis 1 Actual Groups I 1 I Croup I 1 M i c t e d Group Membership No. ofCases 94 Percent of "grouped"cases correctly dassified: 5238% Table 18: Classification Results for Cases Not Selected for Use in the Analysis Group 1 1 Actual Groups 1 Predicted Group Membership No. of Cases I 2 3 I 37 18 48.696 13 35.18 6 16.2% 2 41 24.4% 10 16 39.0% 36.6% 3 40 14 35 .O% 1O 25.0% 16 40.046 Percent of "grouped"cases correctly classified: 4237% 15 4.6.2 Demographic Measures as Predictors The 13 demographic measures used in the discriminant procedure were as follows: employment status (white collar vs. blue collar): household size; gainfully employed in the workforce or not; gender; education; Iive in British Columbia; live in Quebec; live in Atlantic provinces; live in Prairie provinces; live in Ontario; age; marital status; household income; in the second run of the discriminant procedure. demographic variables were used to see if demographic indicators could be useful in predicting cluster membership. Though the two discriminant functions generated were not significant at the 95% confidence interval, a greater proportion of prescription dnig users were conectly classified than could have been expected by chance (47.7% correctly classified versus 33.7% by chance). Tabie 19: Classification Results for Demographic Predictors 1 Group 1 Percent 1 1 Actual Croups 1 Predicted Group Membership No.of Cases 1 2 3 I 133 44 33.1 % 60 45.1% 29 2 1.8% 2 165 29 17.6% 1 07 64.8% 29 17.6% 3 130 16 12.3% 46.9% - - of "gmupdmcases correctly classificd 47.66% 61 53 40.8% Using the demographic indicators. two discriminant functions were calculated. with a combined x2(24)=35.56. p C. 10. After removai of the first function. there was no strong association between groups and predictors. The Tint discriminant function itself accounted for 64% of the between-group variability (Table 20). Table 2û: Canonical Discriminant Functions Function Pe-nt of Vmance Cumulative Percent of Variance WilksO Lambda Chi-Square df Significance tevel 1 64.09 64.09 0.92 3556 24 .O6 2 35.9 1 100.00 0.97 12.87 1i 30 Examination of the group centroids shows the first discriminant function maxirnally separates Cluster 3, the Uninformed Followers. from the other two cluster groups. Table 21: Canonical Discriminant Functiom Evaluated At Croup Means Cluster Croups I Funcuon t I Function 2 The loading matrix of comlations between predictors and discriminant functions. as seen in Table 22, suggests that the best predictors for distinguishing between cluster 3. the Uninformed Followers and the other two groups (fust function) are employment status (STATUS-N) (i.e. white collar vs. blue collar). household sire ( H H S I E ) . whether respondent is gainfully employed, unemployed or retired (EMPLOY-N). age I (RESP-AGE) and gender (VAR40). As shown in Table 23. Clusrer 3, the Uninformed Followen are more iikely to be retired (rnean=3.24) than the System Skeptics (mean=2.95) and Confident Decision Makers (mean=2.74), tend to live in smaller sized households (mean=2.24), and are less likely to be employed in the workforce (mean= 1-42 vs. 1.47 for System Skeptics and 1.56 for Confident Decision Makers). Uninfomed Followen also tend to be slightly older than the other two cluster groups. bom in 1939 venus 1945 for System Skeptics and 1944 for Confident Decision Makea, and are less likely to be female (mean=1.72). The other discriminant function was not interpreted because it did not approach statistical significance at either the 95% or 90% confidence interval. Table 22: Results of Discriminant Function Analysis of Demographic Variables 1 1 Predictor Variables I (HHSIZE) Houehoid Sue 1 Correlations of mdictor variables I l 1 1 -53 1 1 Univariate R2.425 1 2 1 -16 1 4.7191 GENDER WARW -Al -, 18 2.204 1 Resident of 6.C -27 -.22 12113 Education Level (RESP-LN) -21 .W .5 109 Resident of Atlantic Provinces -.O4 .O 1 .O222 (RESP-EE) -51 -56 5.1476 Resident of Prairies (PRAIRIES) - .O9 -43 1.3096 Marital Status (MAUT-N) -.19 -33 1.1493 Household lncome (HHI) .O7 -22 .3798 (BC) Residentof uebec (QUEB& (ATLANTIC) Age of Res ndent 1 Resident of Ontario (ONTARIO) ( -08 1 -.I2 ( .l766 Table 23: Gmup Means by Demwaphic Predictor Variables Cluster Groupings I h Predictor Variables I 2 3 Em loyment Sianis &TATUS-N) 2.95 2.74 3 -24 Household Size (HHSIZE) 2.67 2.6 2.24 GainfuiIy Empfo ed/Unem loyed 1.47 156 I -42 GENDER WARW Age of Res ndent 1 -76 1 -83 1.72 1944.08 19395 &PLOY-PI) (RESP-EE)1945.78 The stability of the classification procedure for the demographic discriminant analysis was checked by a cross-validation run. Approximately 25% of the cases were withheld from calculation of the classification functions. For the 75% of the cases from whom the classifications were derived, there was a 45.3% correct classification rate. For the cross-validation cases, 42.5% were correctly classified. However, the development of an accurate function was not possible at an appropriate confidence level using crossvalidation. Therefore. the results can not be confidently be considered stable. 4.6.3 Situational Measures as Predictors Situational measures refer to elements that describe the outcornes and processes of prescription dmg use. The 15 situational measures used in the discriminant procedure were as follows: 1. 2. 3. 4. 5. 6. level of satisfaction with information given by the pharmacist about the dmg; level of satisfaction with information given by the doctor about the drug; level of satisfaction with information given by the pharmacist about the condition; level of satisfaction with information given by the doctor about the condition; overall level of knowledge about the drug prescribed; received written information from the doctor about the drug; received written information from the pharmacist about the drug; received written information from the doctor about the condition; received w ~ t t e ninformation from the pharmacist about the condition; illness from which patient suffers: number of visits to doctor in last year. type of drug purchase: type of condition (chronic vs. episodic); number of drugs taking; drug plan coverage; The third, and final, discriminant mn used charactenstics related to the respondent's health, and their satisfaction with elements related to their health in order to determine if these variables could be used to predict group membership. Through this procedure. two discriminant functions were calculated, with a corn bined x2(48)= 133-40, p c.01. After removal of the first function, there was no strong association between groups and predictors. The first discriminant function accounted for 84% of the between-group variability (Table 24). ! 24: Canonical Discriminant Functions For Situational Variables Function Percent of Variance Cumulative Wilks' Lambda I 84.16 84.1 6 2 15.84 100.00 Percent of Variance Signifrcmce ChiSquare df 0.60 133 -40 48 -00 0.9 1 24.33 23 -39 Level Examination of the group centroids shows the fint discriminant function maxirnally separates Cluster 1, the System Skeptics, from the other two cluster groups. Table 25: Canonical Discriminant Functions Evaluated At Group Means Cluster Croups Function I Function 2 1 1 . 1 1946 -.O0903 2 -.44549 .32512 3 -.47747 -.4Z102 The loading maîrix of comlations between predictors and discriminant functions, as seen in Table 26. suggests that the best predicton for distinguishing between cluster I l the System Skeptics and the other two groups (first function) are satisfaction levels with the information given by the pharmacist and doctor about the dmg, and about the condition. as well as knowledgeability about the clmg prescnbed. Anaiogous to their name. Cluster 1. the System Skeptics tend to be more dissatisfied with the information provided by traditional health care providers about the dmgs they prescribe or dispense. and about the conditions for which they m a t As shown in Table 27. this group is less inclined to report high levels of satisfaction with the pharmacist in terms of the information provided about the drug (mean=2.2 1, where l=very satisfied 4= not at al1 satisfied), as well as about the condition for which they are being treated (mean=2.64). The System Skeptics tend to be dissatisfied with the information provided by their doctor about the drug they were prescnbed (mean=2.23) and about the condition from which they suffer (mean=2.15) (Table 27). Possibly as a function of the dissatisfaction they express with traditional health care professionals, they also report the lowest level of knowledge about the drugs they were prescnbed (meand. 10)compared to Confident Decision Makers (mean=5.20) and Uninforrned Followers (mean=4.96). Table 26: Results of Dixriminant Function Analysis of Health Characteristics Predictor Variables Satisfaction with information iven by phamacist about drug IB) Satisfaction with information iven by doctor about d m g (VARA A) Satisfaction with infoyation iven b pharmacist about condition $AR 18d) Overali level of knowled e &out dmg prescribed (VA1 (vA7) Satisfaction with infolmation iven by doctor about condition (V 1 8 ~ ) Received wrïtten information fmm doctor about dnig (VAR IOA) Suffer from Res irato problems di (RESB~RA~ Received written information from pharmacist about dnig (VARIOB) Number of times visited doctor in last year NAR321 Received wrîtten information from doctor about condition (VAR 17A) Type of dnig purrhase (VAR2) Received wtitlen infornation from harmacist about conditton (VAR1 Type of condition chronic vs. short-tem (VAR6B) Suffer frorn dermatolo ical problerns (DERMAT~L) Suffer h m rniscellaneous illnesses d) (OTHER) Nurnber of dmgs taking at given time (VAR33) Suffer h m OblGyn problerns (OBGYNE) Suffer fiom Bowel problerns (BOWEL) Suffer frorn Musculoskeletal problems (MUSCULO) Covered b dnig plan Univariate F(2.4 15) Correlations of p d i c t o r v-ariables with discriminant functions 2 I -0.1 0.7 1 , 36.024 1 0.58 0.04 24.1717 0.42 0.09 12.8267 439 0.2 1 1 1.4448 0.39 O. 14 10.8569 0.28 0.05 5.4905 I I "-" I 0.18 0.06 2.3778 -0.17 -0.02 2.0752 -0.11 2.0772 0.15 0.15 -0.09 0.1 3 1.8796 1.624 0.14 037 3.O989 0.02 0.33 1.4813 -0.03 -0-3 1.3127 4-23 0.05 -0.26 0.25 -0.23 4.7864 1 .O202 1.1844 0.16 4.08 ' ' - 4.02 0.2 1 0.63 14 0.05 0.2 0.7 182 -0.03 0.16 0.4 154 4.03 0.1 2 0.24 14 0.0 1 -O. f 0.1 1 -0.1 1 0.1861 0.8987 O 0.04 0.02 12 (vAK34) Suffer from Endocrine problems (ENDOCRIN) Suffer from Nutrition pmblems ( N m m Suffer from Pain problems ( P A N ) Suffer frorn Cardiovascular problems (CARDIO) Suffer from Mental Health problems (MENTAL) ' 1 Table 27: Group Means by Predictor Variables I 1 PRdictor Variables Satisfaction with-information given by pharmacist about dmg (VARI IB) 1 l Cluster Groupings 1 1 2 1 3 2.2 1 1.41 1.45 2.15 1.73 1.64 1 --- Satisfaction with information given by doctor about dmg (VARI I A) Sahsfaction with in-nnation given by phmacist about condition (VARI SB) Overall level o f knowledge about dm rescribed WU7, Satisfaction with infonnatjon given by doctor about condition (VAR1 SA) The classification results indicate that a total of 52.2% of the cases were correctly classified, compared to 38.5 % that would be comctly classified if al1 respondents belonged to the largest cluster grouping, or 33.7% with a classification accuracy achieved by random or chance grouping. Table 28: CIassification Results for Situational Predictors Predicted Group Membership Actual Groups No. of Cases Gmup 7 3 I 129 77 59.7% 34 26.46 18 14.09 2 16 1 26 16.1% 99 61.5% 21-48 3 128 10 70 54.78 32.8% 1 2.5% 36 42 Percent of "grouped"cases correctly classified: 52.15% The stability of the classification p r o c e d u ~was checked by a cross-validation run. Approximately 25% of the cases were withheld from calculation of the classification functions. For the 75% of the cases from whom the classifications were derived, there was a 59.0% correct classification rate. For the cross-validation cases, 40.5% were correctly classified, though the sarnple size for this classification procedure was too small for accurate classification. Table 29: Classification Results for Cases Selected for Use in the Analysis Gmup I I Actual Gmups 1 62 64.6% 96 1 1 Predicted Gmup Membership 25 26.0% 9 9.38 1 I Percent of "grouped"cases correctly classified: 58.96% Table 30: Classification Results for Cases Not Selected for Use in the Analysis 1 1 Actul Gmups No. of Cases Gmup I 33 2 42 3 36 1 Predicted Gmup Membership 1 2 3 424% I4 11 33.3% 8 24.2% 6 14.3% 45.2% 5 13.9% 19 19 52.8% 17 30.55 12 33.3% Percent of "grouped" cases correctly classified: 40.54% 4.7 Logistic Regression In addition to the discriminant analysis pmcedures, a logistic regression was conducted in order to better identify the demographic variables that discnminated arnong cluster groups. This procedure used cluster membership as a dichotomous dependent variable and both continuous and categoncal demographic indicators as independent variables. Logistic regression was used in this case because the demographic variables were non-normally distributed. However, in order to accommodate 3 cluster groups as the DV, three separate analysis had to be performed. The fint mn of the logistic regression procedure used cluster group 1, the Systern Skeptics and cluster group 2, the Confident Decision Makers as the dependent variable. The second logistic regression analysis used cluster group 1. the System Skeptics and cluster group 3, the Uninformed Followers as the DV, while the third, and final, exarnined cluster group 2 and cluster group 3 as the dependent variable. The first run used cluster 1 and cluster 2 as the dichotomous dependent variable, and the following demographic indicators as independent variables: gender; household size; household income; age; marital status; education level; empioyment status; and, province of residence. The likelihood value (-2LL) examining cluster 1 versus cluster 2 was calculated to be 392.96. According to Hair et al. (1987), a small-2LL value indicates a well-fitting model. An assessrnent of the fit of the model can also be assessed by creating a classification table which compares the actual events versus the predicted values. As seen in Table 3 1, 63.4% of the cases are correctly classified. However, a more detailed examination of the correct classification for the individual groups indicates that cluster 1 was not predicted as well by the independent variables as cluster 2. Cluster 1, had a correct classification rate of only 45.996, compared to 77.6% correct classification for Cluster 2. Table 31: Classification Matrix Using Demographic indicators to Predict Group Membership 1 I 1 I Observed I Predicted I 1 1 I Comct Classification 2 1 1 Overail classification: 63.42% Two individual predictors, gender and age contributed significantly to the classification of cluster 1 versus cluster 2. The second logistic regression that was run used cluster group 1 versus cluster group 3 as the dichotomous dependent variable. and the demographic variables as independent variables. For this analysis. the likelihood value (-2LL) exarnining cluster 1 versus cluster 3 was calculated to be 347.15. An assessrnent of the fit of the mode1 was also assessed by examining the classification table comparing the actual events versus the predicted values. As seen in Table 32, 63.1% of the cases are correctly classified. Both Cluster I and Cluster 3 had a correct ciassification rate of 63.1%. Table 32: Classification Matrix Using: Demographic Lndicators to Predict Group Membership I I Predicted Observed 1 3 Comct Classification I 84 49 63.16 3 48 82 63.O8 1 Overall classification: 63.12% I 1 The only predictor that was significant at the .O5 level was the respondent's age. The third, and final, analysis used cluster 2 versus cluster 3 as the dichotomous dependent variable. In this case, the likelihood value (-2LL) examining cluster 2 versus cluster 3 was calculated to be 380.17, An assessrnent of the fit of the mode1 was also assessed by cnating a classification table which compared the actual evenü versus the predicted values. As seen in Table 33,6 1.7% of the cases are correctly classified. However, a more detailed examination of the correct classification for the individual groups indicates that cluster 3 was not predicted as well by the independent variables as cluster 2. Cluster 3, had a correct classification rate of only 40.0%. cornpared to 78.8% correct classification for Cluster 2. Table 33: Classification Matrix Using Ikmographic Indicators to Predict Group Mernbership Predicted Observed 2 1 3 Correct Classification 1 Overall classification: 6 1.69% Three individual predictors. gender, household size, and residence in the province of Quebec contributed significantly to the classification of cluster 2 versus cluster 3. 4.8 Multinominal Logit Multinominaf logit was used to confirm the logistic gre es si on analyses. According to Tabachnick & Fidell (1989), logit analysis is better in situations where the dependent variable has more than 2 categoties because it has no pararnetric assumptions 1 that are likely to be violated. in the logit model, the 3 cluster grouping was used as the DV,and the demographic indicators were used as IVs. The demographic indicators used were as follows: gender; household size; household income; age; marital status; education levei; employment status; and, province of residence. The overall model was not significant at the 90% or 95% confidence interval (x2=29.5, It is possible that in the original analysis a significant result was obscured by error variance from irrelevant IVs. Specifically. the original analysis was conducted on 13 independent variables. which resulted in 22 degrees of freedom. If a similar chi square result can be obtained with less degrees of frccdom (Le. less variables). selected demographic variables rnay indeed predict cluster membership. Consequently. a second analysis was conducted using a reduced set of IVs. It was hoped chat by focusing on fewer variables significant results would not be obscured by "noise" from erroneous IVs. The IVs used in this analysis were as follows: gender; household size; household income; age. The overall mode1 was significant at the 95% confidence interval (x2=21.1, d.f.=S. ~ ~ 0 5 ) . As shown in Table 34, Cluster 1, the System Skeptics, are defined only by their year of birth. Members of this group are more likely to be bom in the 1960's (36.24%) than in the 1930's (27.49%). Gender, household size, and household income do not predict membership in Cluster 1. Cluster 2, the Confident Decision Makers, are defined by gender and household size. Members of this group are less likely to be represented by men (29.15%) compared to women (41.94%), and are more likely to live in dwellings of 4 or more people (44.55%)than single person dwellings (32.87%). Age and household income do not predict membership in Cluster 2. Cfuster 3. the Uninfomed Followers, are defined by gender, year of birth and household size. They are more likely to be represented by men (36.48%) than women (28.04%), are more likely to be bom in the 1930's (33.1 1%) versus the 1960's (25.938). and are more likely to live in single person dwellings (37.86%). Table 34: Prodictecl Percenîages Based on Coefficients from LIMDEP Output 1 Base I Clrister 1 I Cfmter 2 l 3 1-15 l 38.92 I Cluster 3 I 29-94 I Gaidcr: Men 3437 29.15 36-48 Women 30.02 4 1 -94 28-04 Boni in 1930 27.49 39.4 33.1 1 Born in 1950 33.21 3853 28.26 Born in 1960 36.24 37.83 25 -93 4 or more 32.18 4455 23 -27 Y a r Born: V. DISCUSSION In this section of the report, a summary of the results and conclusions will be presented, along with a discussion of the implications and recommendations flowing from the results. 5.1 Introduction The purpose of the research was to identify whether distinct segments of prescription drug users existed by classifying consumers according to their sirnilarity on attitudinal dimensions related to their health. prescription dnigs, and the conditions from which they suffer. Following this, the goal was to profile these segments on demographic. behavioural and situational descriptors to better understand the composition of each cluster grouping. It was thought that such a typology would be useful in providing a descriptive account of how various groups of prescription drug usea think and act. thereby, enabling various stakeholden to develop marketing communications and consumer educational programs aimed at the different target groups. The main results of this study lead to the conclusion that, in the sample studied, there are different segments of prescription drug usen, which c m be inferred from their similarity on attitudinal dimensions. However. traditional demographics variables only weakly predicted group membership. This weakness will hinder efforts to identify and thus ultimately influence System Skeptics. Confident Decision Makers, and Uninformed Followers. Keeping this in mind. the following section will discuss how different communications programs and educational progmns could be developed to reach each of the target groups identified in this study. and how the results. in particular, may be useful for d i f f e ~ nstakeholder t groups. 5.2 Attitudinal Dimensions Analyses of the 32 attitudinal variables indicated that. for this population of prescription dmg users. there were eight psychographic dimensions. These dimensions comsponded to infomation involvement, information avoidance, self-assured knowledge. self-care orientation, manufacturer-oriented information, doctor-oriented information, pharmacist-onented information. and patient decision making. Al1 the variables loading highly on the fmt psychographic dimension. information involvement, stressed concem about acquiring information about medications either independently through written matenals, or by asking questions of health professionais. The second psychographic dimension, information avoidance, was characterized by barriers. or inhibitors to receiving information about medications. The perceived diff~culty in understanding the information. the doctor's use of language. the phannacist's lack of visibility, and the lack of pnvacy at the pharmacy were deemed to represent baniers to receiving this information. The third psychographic dimension, self-assured knowledge. was defined by three items. The three statements that loaded highly on this factor weh the perception that they are more knowledgeable than others about the condition frorn which they suffer. and of the medication they take. and in knowing where to fmd al1 the information they need. These variables. in combination. were deemed to represent the patient's perceived knowledgeability about prescription medications. The variables loading highly on the fourth psychographic dimension. self-care orientation, focused on the desire to take control of one's health and treatment decisions, rather than relying on doctors to make these decisions on their behalf. Negatively conelated items on this factor were, "1 wouId rather have the doctor make the decisions about my treatment than for him or her to give me a whole lot of choices". and 'There is no need to ask questions about prescription dmgs if you mist the doctor". This factor was characterized by the patient's desire to take a proactive role in their healthcare decisions, and. correspondingly. to rely less on traditional healthcare providers. The fifth psychographic dimension. manufacturer-oriented information was charactenzed by four variables. Two of the four variables had loadings of .65 or more ( 2 4 "Dmg companies ought to inform consumen about health issues and medications"; 24D 'The Company who makes the dmg should tell me what 1 need to know about my medication*'),while the other two (24DD"It would be helpful if the doctor provided wriiten information about the dmgs helshe prescribes"; 24T "1 want information about my prescription dmg so 1 can determine if the medication is working or not") had significantly weaker loadings of .34 and .32 respectively. Consequently, this factor was deemed to principdly represent prescription dmg users' desire for dmg manufacturen to be involved in providing information about the dmgs they manufacture. The sixth psychographic dimension. doctor-oriented information. was defined by three items. The three variables were related to the approachability of the doctor in answering patient questions, the doctor's role in providing information to patients. and the patient's assertiveness in asking the doctor questions about the medication prescnbed. These variables represented the "doctor" factor. The seventh variable. phannacist-onented information, was also defmed by three items. These three variables were associated with the pharmacist's role in providing information to patients, the patient's assertiveness in asking the phannacist questions about the medication prescribed, and the perceived accessibility of the pharmacist at the pharmacy counter. These three variables ~presentedthe "phannacist" factor. The eight. and final. factor, patient decision making, was charactenzed by ihree items which were related to the patients' desire for making decisions regarding their medications. These decision making items were 1) whether to take the medication or not. 2) to determine whether the medication was working or not, and 3) in making choices of which medication to take among a set of available alternatives. 5.3 Psychographic Segments The cluster procedures resulted in the population of prescription drug users being classified into three different groups on the b a i s of the similarity of each drug user's score on each of the attitudinal dimensions. These groups of consurners. together. made up the typology of prescription drug usee. 5.3.1 Cluster#1 -SystemSkeptics The System Skeptics were distinguished by their tendency to lack faith in traditionai heaithca~providers -- narnely. doctors and pharmacists. Aititudinally, they were more Likely to perceive barries to receiving prescription d m g information, particularly from health professionais; and appeared to lack confidence in their ability to make informeci health care decisions. Funher, they expressed more discontent with the accessibility of doctors and pharrnacists, particularly when it coma to providing information to patients about prescription medications. They were the least Iikely to feel that both doctors and pharmacists provided thern with information about their medication, and they were the least likely to ask questions about their medication frorn these professionals. The System Skeptics can be profiled dong a number of behavioural. demographic and situational descriptors that were exarnined. Behaviourally, they were less likely to report that they receiving counselling from both the doctor and pharmacist regarding their condition and of the prescription medication they were prescnbed. Further, they were among the least satisfied with the information that is k i n g provided by doctors and pharmacists. They also claim to be the least knowledgeable about the dmgs they were prescnbed -- possibly as a function of their perceived lack of assistance from hedth professionals. Demographically, age was the only variable that distinguished the System Skeptics from the other two cluster groups. They tended to be younger than their counterparts in the other two groups -- bom in the 1960's rather than the 1930's. 5.3.2 Cluster #2 - Confident Decision Makers The Confident Decision Makers can be distinguished by their more positive and proactive orientation to decisions about their health. Not only were they more likely to take an active role in seeking out information about their medications from friends and family and published materials, they tended to feel more knowledgeable and, expressed comfort in taking their medications when they have this information in hand. Confident Decision Makers also more often wanted to play a greater role in treating themselves, and in making decisions about their medication. in particular, they were more likely to feel they should be relying on doctors l a s , and relying more on themselves for these types of decisions. Despite this orientation. they morp often appeared to be receptive to information from a variety of channels. They felt that manufactures should provide patients with the information they need to know about their medication, d o n g with information from doctors and pharmacists. Their willingness to receive information fiom a variety of sources appears to stem from their desire to make educated health decisions. The Confident Decision Makers were not predicted well by the behavioural. demographic and situational descriptors that were examined. No behaviour nor situational descnpton distinguished this cluster grouping from the other two groups. Demographically. gender and household size were the only variables that distinguished the Confident Decision Makers from the other two cluster groups. In particular, they were more heavily represented by women, and those living in larger-sized households of 4 or more people. 5.3.3 Cluster #3 - Uninformed FoIlowers The Uninformed Followers were distinguished by their lack of desire to be involved in decisions affecting their health. They tended to be much more cornfortable leaving these decisions to traditional healthcare providers -- namely, docton and pharmacists. Attitudinally, they were less likely to perceive barriers to receiving prescription dmg information. However. they less often wanted to bear the responsibility of making medication decisions thernselves. This group of consumers were more confident in placing these decisions in the hands of traditional healthcare providers - doctors, and to a lesser extenc pharmacists. The Uninformed Followers can be profiled dong a number of behavioural. demographic and situational descriptors. Behaviouraily, the Uninformed Followers were the least likely to seanih for information about their condition and of the drug they were prescribed; and cited fewer sources when they actually did conduct a search for this type of information. They were also less likely to ask questions of their pharmacist or doctor about the drug they were prescnbed - consistent with their desin and comfort in leaving these types of decisions to traditional healthcare providers. Demographically, employrnent status, household size, age and gender were the variables that distinguished the Uninformed Followers from the other two cluster groups. They tended to be older, male, retired, and Living in smaller-sized households. 5.4 Implications and Recommendations The results of this research have implications for a number of stakeholders, including govemment, health professionals. pharmaceutical manufacturers, and retailes. Distinct groups of consumers existed based on their attitudes toward their health. prescription dmgs, and the conditions from which they suffer. Understanding the motives that underlie consumer interest or disinterest in their medications and framing communications that seek to meet the informational needs identified may help to encourage patients to play a more active role in the decisions affecting their health. However. it is important to note that efforts to target information appropriately will be hampered by the poor ability of the assessed demographics to predict the key consumer groups and the dificulty in identifying people by their attitudes alone. Given the different objectives of various stakeholders (i.e. government agencies. health professionals, pharmaceuticals manufacturers. and consurners), the fuidings and implications of this research differs. The subsequent section will discuss the relevance of these findings in the context of the objectives of these stakeholder groups: health ministries, physicians, manufafturers, pharmacists, and consumen. First, the fedeml and provincial health ministries have an interest in the area of information search and prescription drug usen. given that their mandate is to fund a system that improves the health and well-king of the public, to educate the public about proper dmg utilization. and to reduce healthcare costs. This research identifies that there are attitudinal differences among prescription drug users - each with a different orientation to the traditional healthcare system, and the role the patient plays in this system. System Skeptics tend to be less positive about the role of traditional healthcare providers and want less involvernent from these professionals, while the Confident Decision Makers want to take a more proactive role in the decisions involving their health alongside traditionai healthcare providen. Uninformed Followers, on the other hand, want to leave these issues in the hands of traditional healthcare providen. Although untested in this research. it is possible that a relationship exists between a patient's active role in their healthcare decisions, and their overall health and well-being. It is postulated that if patients play a more active role. they may be more inclined to provide more information to the doctor at the tirne of diagnosis or to the phannacist at the time of purchase. in terms of discussing symptoms. side effects. and the List of the drugs they are taking at the present time so that complications from dmg interactions can be mitigated. and more educated decisions can be made frorn the doctor's perspective. if such a positive relationship exists. it may result in fewer visits to the doctor. thereby reducing health care costs, and may also lead to greater compliance with the prescribed regimen. Greater cornpliance would be a cost-saving measure as well. given that roughly 1 3 4 of hospitalizations among the elderly is due to incorrect use of prescription medications (Morris et al., 1994). if' this relationship is confirmed through empirical testing, it may be useful to embark on an educational campaign that moves prescription dmg users towards this proactive role by focusing on the benefits that can be achieved through active participation in heaithcare decisions. Second. the physician's mandate is to mat patients by curing illness and promoting wellness and well-being. This research identifies that there are diffe~ncesbetween groups in terms of their interactions with traditional healthcare providers. For exarnple. System Skeptics do not feel they are adequaiely being counselled by their physician about the drug prescribed and about the conditions frorn which they suffer. while Confident Decisions Maken want to be told about al1 of their available treaûnent options in order to arrive at an educated decision in conjunction with their heaidicare provider. Uninfomed Followers. on the other hand, don? want to be involved in the decisions involving their health; they would rather leave these decisions in the hands of their physician. Therefore. this research may be useful to physicians in recognizing that differences exist among different patients. thereby ailowing them to tailor their "bedside mannef' according to the unique desires of their patients. This research suggests that Confident Decision Makers more than iikely want detailed information at the time a dmg is prescribed. and more emphasis given to discussing their avaiIable alternatives. On the other hand, Uninformed Followers want to rely solely on the physician to make decisions on their behalf. They probably don? want a s much information as the Confident Believers. System Skeptics appear to want information, but perhaps not from the physician, yet they feel they are not getting proper information from these healthcare providers. Information outside of the doctor's office. such as videos, brochures. and diagnostic software may be useful for this segment. Sensitivity should be given to this segment, however. given their apprehensive attitude towards physicians. Third, the manufacturer's mandate is to sel1 more drugs by encouraging physicians to prescribe their drugs over another manufacturer's. This research is useful to manufacnirea because it identifies that there are difkrences between the groups in tems of their interactions with physicians, as well as in their intentions to specifically ask for a specific h g . The goal of encouraging physicians to prescribe a specific dmg could possibly be achieved by providing appropriate informational materials to physicians so they can properly address patients' questions. Furthemore, pharmaceutical manufacturers could develop educational materials that could be passed on to consumers via the physician, with the airn of encouraging patients to ask for a specific medication. Given that Confident Decision Makers are more likely than the other two segments to ask a physician to prescribe a specific medication. rnanufacturers would probably want patients to move towards this more proactive segment, if they are in fact requesting a product in which they manufacture. Manufacturers could also use this information to tailor their educational materials depending on the needs of the patient. For exarnple. Confident Decision Makers are more likely to want information detailing their available options, including (but not limited to) the manufacturer's product; while the Uninformed Followers are probably more inclined to want simple, easy-to-read infomatioii that their physician c m explain to them at the time of their appointment Fourth. the phmacist's mandate is to dispense the appropriate medication to consumers. to encourage corn pl iance and reinforce the information given by the ph ysician. as well as to encourage repeat purchases at the pharmacy. This research identifies that there are differences between groups in terms of their attitudes towards phamacists as well. Sirnilar to their interactions with physicians, System Skeptics do not feel they are adequately being counselled by their pharmacist regarding the dmg prescribed or of the condition from which they suffer. They also perceive the greatest barriers to obtaining this information at the pharmacy due to a perceived lack of accessibility of the phannacist and of a lack of privacy at the pharmacy counter. Due to these perceived baniers, it rnay be useful to promote the role of the phannacist by moving hem in front of the counter, thereby making them appear more accessible. Establishing counselling areas beside the dispensing counter may also prornote the accessibility of the pharmacist, as well as creating a more private environment for its customen. This information may allow pharmacists to tailor their counselling activities depending on the needs of their customers. Again. Confident Decision Makers more than iikely want detailed information from the phamacist at the time of purçhase to reinforce the information supplied by the physician. or if information has not been provided, to educate them about their available alternatives. Pharmacists that offer such information wiU likely be more attractive to Confident Decision Makee than phmacists that do not On the other hand, Uninfonned Followen probably want to rely solely on the information supplied by their physician. This group simply wants to have their prescription filled. System Skeptics, on the other hand, appear to want information, but may be better reached through point-ofsale materials (e.g. brochures), video iibraries or selfdiagnostic tests available in the pharmacy. They rnay also be receptive to the concept of more pnvate counselling areas, although this is speculative and has not been tested in this research. Finally, the consumer's goal is to protecf and promote their o w n health and well- king. This research is useful to patients by virtue of the fact that it identifies that there are like-minded groups of patients in the Canadian population. sharing the sarne beliefs and concems as themselves. Knowledge of other people with similar information concerns may motivate particular patient groups (e.g. Confident Decision Makers) to organize themselves into discussion or consumer advocacy groups, with the mandate of promoting more active participation in their heaith. Such advocacy groups will likely enhance the patient's overall health and well-being by creating an environment which promotes an exchange between patients and healthcare providers that will allow for more informed decisions to be made. 5.5 Recommendations For Future Research This section discusses areas of improvement for future research that rnay be undertaken in the field of information search behaviour and prescription drug users. Fit, future research should be directed at testing the reliability and validity of the cluster groupings. In particular. it would be desirable to test the stability of the cluster groupings by repeating the study at another t h e . Though other natural grouping may have existed in the data set - which would have clustered subjects into different hornogeneous categories - of al1 the solutions attempted. the present solution offered the most distinct, homogeneous and interpretable groupings. Greater confidence could be p laced in the results if future research validated the results gleaned from this study. Second. this study was conducted with prescnption drug users who were part of a consumer mail panel. Consumer mail panels are a self-selected group which may differ in some relevant and systematic way from prescnption users in general. In the future. it would be desirable to test the reliability of this research by repeating it with a group of randomly selected prescription drug users to see if the sarne results are obtained. Third, the sarnple used in this research was repmented more heavily by those refilling a prescription medication than those filling new prescriptions (72% vs. 2856). It could be postulated that users filling a new prescription may hold different attitudes and engage in different behaviours than those simply refilling or repeating a prescnption. Future research may want to examine the different strategies employed by these two groups of prescription drug users. in addition to the proposed usefulness of exarnining differences between those filling new prescriptions versus those refilling a prescnption. the sarnple was also comprised prirnarily of prescription dnig users who were taking their medication for the treatment of a chronic illness (70%)rather than for an acute or temporary illness (30%). Given these two issues. it may be useful to segment based on usage patterns rather than demographics, psychographics, benefits or behaviours in future research studies regarding information search and prescription drug users. In addition to using usage patterns as the basis for segmentation, it may also be useful to conduct a segmentation based on demographics. using age as a key variable. since older prescription drug users held different attitudes than their younger counterparts. in this siudy, the sample was comprised prirnarily of elderly prescription drug uses (45%were 55 years of age or older; 2 8 4 were 65+)than non-elderly drug usea. Previous lesearch has also identified that health professionals interact and provide different information to these two groups of patients (Morris et al.. 1987). Therefore. future research may ais0 want to examine differences between younger and older prescription h g users. Fourth, in the case of scale development, it would be advisable to continue external validation. Presently, these scales have k e n validated against self-reporteci behaviours of information search (e.g., the CoriTident Decision Maken who scored highly on information Involvernent were more likely to report they had searched for information about their drug and condition and had used a greater number of sources for this purpose). It would further validate these scales if they could be associated with observed. rather than self-reported. behaviours. Fifth, after further examining the eight factors denved frorn the Principal Axis Factoring rnethod. it may be helpful to include a greater number of variables related to knowledge, decision making, and the doctor and pharmacist to see if additional variables would load on the four factors deemed to repnent "self-assured knowledge". "doctororiented information", "pharmacist-oriented information" and "patient decision making". Presently, each of these factors only had three variables with loadings of .3 or more. 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Journal of Marketing Research, XVI, 303-312. - APPENDE 1: RESULTS FROM PRINCPAL COMPONENTS ANALYSIS 1O9 -> FACTOR /VARIABLES var24a var24b var24c var24d var24e var24f var24g var24h var24i -> var24j var24k var241 var24m var24n var240 var24p var24q var241 var24s -> var24t var24u var24v var24w var24x var24y var242 var24aa var24bb var24cc -> -> var24dd var24ee var24ff /MISSING MEANSU' /ANALYSIS var24a var24b var24c var24d var24e var24f var24g var24h var24i var24j var24k var241 var24m -> var24n var240 var24p var24q var24r var24s var24t var24u var24v var24w -> var24x var24y var242 var24aa var24bb var24cc var24dd var24ee var24ff -> -> /PRINT INITIAL EXTRACTION ROTATION -> /FORMAT SORT /PLOT ROTATION /CRITERIA MINEIGEN (1) ITERATE ( 2 5 ) -> /EXTRACTION PC -> /CRITERIA ITERATE(25) -> /ROTATION VARINAX -> /SAVE REG(ALL) . 110 _ _ _ _ _ _ _ _ _ _ _ A N A L Y S I S - - - - - - - - - - - Replacement of missing values w i t h the mean Analysis number 1 Extraction F A C T O R 1 for analysis Principal Components Analysis Initial Statistics: Variable PC Cornmunality extracted 9 factors. Eigenvalue ~ c of t Var C m Pct - - - - - - - - - - - A N A L Y S I S F A C T O R - - - - - - - - - - - F a c t o r Matrix: Factor 1 Factor 2 Factor 3 Factor 4 Factor 6 Factor 7 Factor 8 Factor 9 Factor 5 - - - - - C _ _ - - F A C T O R - * Variable VARIMAX VARI= rotation Factor 1 for e x t r a c t i o n - - - - - - - - - - - A N A L Y S I S Eigenvalue P c t of Var 1 i n analysis 1 - Cum Pct Kaiser Normalization. converged i n 2 3 i t e r a t i o n s - Rotated Factor Matrix: Factor Factor Factor Factor Factor - - - - - - - - - - Factor A N A L Y S I S F A C T O R Factor 6 7 Factor 8 - - - - - - - - - - Factor 9 F i n a l S t a t i s tics : Variable * * * * * * * f * Factor 1 2 3 Eigenvalue 5 5.14317 3.51780 2.14859 1.67526 1.46265 4 6 1.25428 7 1.18550 8 1.14203 Pct of V a r Cum P c t APPENDIX II: RESULTS FROM PRINCIPAL M S FACTORING -> FACTOR 11s -> /VARIABLES var24a var24b var24c var24d var24e var24f var24g var24h var24i -> var24j var24k var241 var24m var24n var240 var24p var24q var24r var24s -> var24t var24u var24v var24w var24x var24y var242 var24aa var24bb var24cc -> var24dd var24ee var24ff /MISSING MEANSUB /ANALYSIS var24a var24b var24c var24d var24e var24f var24g var24h var24i var24j var24k var241 var24m -> var24n var240 var24p var24q var24r var24s var24t var24u var24v var24w -> var24x var24y var242 var24aa var24bb var24cc var24dd var24ee var24ff -> -> /PRINT INITIAL CORRELATION SIG DET KM0 A I C EXTRACTION ROTATION -> /FORMAT SORT -> /CRITERIA FACTORS ( 8 ) ITERATE ( 2 5 ) -> /EXTRACTION PAF -> /CRITERIA ITERATE (25) -> /ROTATION VARIMAX . 116 - - - - - - - - - - - Analysis nwnber 1 F A C T O R A N A L Y S I S - - - - - - - - - - - Replacement of missing values w i t h t h e mean C o r r e l a t i o n Matrix: VAR2 4A 1.00000 .15270 ,21918 O4854 -53365 . .28974 .28611 - -00259 -20524 - -00842 - -05290 ,27904 -39488 08459 - ,04382 .O2740 -11970 38149 -09441 ,16417 - ,17038 -12048 -45686 ,24255 .34788 10593 -00968 ,03999 .IO714 -08789 -.O6501 ,10690 -. - - VARS 4H 1.00000 .26466 .29626 VAR2 4F VARS 4G - F A C T O R A N A L Y S I S -- - - - - - - - - - - - F A C T O R Determinant of C o r r e l a t i o n Matrix = A N A L Y S I S .O001886 Kaiser-Meyer-Olkin Measure of Sampling Adequacy = .a0416 B a r t l e t t Test of Sphericity = 3451.7599, Significance = A n t i - M a g e Covariance Matrix: VAR2 4A VAR2 4B VAR2 4C VAR2 4 D VAR2 4 E VAR2 4 F VAR2 4G VAR2 4H VAR241 W24J VARS 4 K W24L VAR2 4M - - - - - - - - - - - - O0000 F A C T O R VAR2 4A .O1509 -. 01847 -. 00631 -.02154 -. 09312 - 02836 -.03172 -01627 -01499 -007611 - 01134 -.06918 .O4044 00687 00941 02596 -.O3699 04243 O0290 -. -. -. -. . VARS 4F ,69434 .O0759 -,02297 ,05118 --O3351 -07595 00743 -.O0386 02734 .O8542 .O8447 04093 .O2160 -.04331 06921 O0510 02094 -.O7999 01034 .O4821 -02293 01504 - .O8419 .O2430 -. -. -. -. -. -. -. -. F A C T O R - - - - - - - - - - - VAR242 VAR2 424A VAR2 4BB VAR24CC VAR24DD VAR24EE VARS 4FE' .54175 .O1707 14413 -.01043 01965 06082 -.03854 -. . -. F A C T O R .65046 - 14365 A N A L Y S I S .72676 --O5185 -. 06228 .O7794 -.O1377 04745 -.O1604 .O1064 .O1036 -. Anti-image Correlation Matrix: - - - - - - - - - - - - 718 90 -.07213 -,10598 .O2191 - - - - - - - - - - - F A C T O R A N A L Y S I S - - 123 - - - - - - - - - - - F A C T O R A N A L Y S I S - ----------- F A C T O R Measures of Sampling Adequacy (MSA) A N A L Y S I S are printed on t h e diagonal. 1-tailed Significance of C o r r e l a t i o n Matrix: ' . ' is printed f o r d i a g o n a l elements. VAR2 4A VAR243 VAR24C VAR24D VAR24E VAR2 4F VAR2 4G VARL 4): VAR241 VAR245 VAR24K VAR24L W 2 4M VAR2 4N VAR240 VAR24P VAR244 VAR24R VAR24S VAR2 4T VAR24U VAR2 4V VAR2 4W VAR2 4X VAR24Y VARS 4 Z - - - - - - - - - - - F A C T O R A N A L Y S I S - - - - - - - - - - - F A C T O R VARS 4K A N A L Y S I S - - - - - - - - - - - F A C T O R VAR2 4V Extraction 1 for analysis A N A L Y S I S VAR2 4W 1, Principal - - - - - - - - - - VAR24X VAR2 4Y mis Factoring (PAF) I n i t i a l Statistics: Variable VAR2 4 A VAR2 4B VAR2 4C VAR2 4D VARS 4E VAR24F VAR2 4 6 VAR24H VAR241 VAR245 VAR2 4K Communality * * Factor Eigenvalue P c t of Var Cum Pct 128 _ _ _ _ _ _ _ _ _ _ _ Factor Variable PAF A N A L Y S I S F A C T O R extracted 8 factors. - - - - - - - - - - - pct of Var Eigenvalue Cum P c t 11 i t e r a t i o n s required. F a c t o r Matrix : Factor 1 Factor 2 Factor 3 Factor 4 Factor 5 - - - - - _ - _ _ - Factor 1 .O1170 -02944 .22479 -25362 ,12988 .37497 .O6447 Factor 6 A N A L Y S I S F A C T O R Factor 2 Factor 3 - - - - - - - - - - Factor 4 Factor 5 -. 17541 .12669 -. 19165 - .13170 -.16506 -12688 .O5884 -,O7904 .13349 .O1496 .15529 ,19583 .25335 .41563 .O3593 03451 .24201 .O9715 .31773 .O9835 ,00268 -21231 .O9744 .15736 .15466 Factor 7 -.00904 -08239 ,28569 Factor 8 -. - - - - - - - - - - Factor F A C T O R Factor 6 A N A L Y S I S Factor 7 - - - - - - - - - - - 8 Factor Transformation Matrix: Factor Factor Factor Factor Factor Factor Factor Factor Factor Factor Factor Factor Factor Factor Factor Factor Factor 1 Factor 2 Factor 3 Factor 6 Factor 7 Factor 8 1 2 3 4 5 6 7 8 Factor 4 Factor 5 APPENDIX DI: RESULTS FROM HJERARCHICAL CLUSTER ANALYSIS 132 -> PROXIMITIES -> s c a l e l scale2 s c a l e 3 scale4 s c a l e 5 scale6 s c a l e 7 s c a l e 8 -> /MATRIX OUT ( ' C :\WINDOWS \TEDfP\spssclus. tmp l ) Data Information 4 3 3 unweighted cases accepted. O cases rejected because of missing value- Squared Euclidean measure used. 134 -> CLUSTER -> /MATRIX IN ('C:\W1NDOWS\TEMP\spss~lus.trnp') -> /METBOD WARD -> -> /PRINT SCHEDULE /PLOTS NONE. * * * * * * H I E R A R C K I C A L 135 C L U S T E R A N A L Y S I S ' * * * * * Agglomeration Schedule using Ward Method Stage 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 Clusters Cluster 1 Conhined Cluster 2 192 127 51 141 39 38 30 77 130 88 26 22 133 103 80 73 14 331 286 132 4 139 158 45 203 36 70 63 10 11 81 322 42 18 233 173 217 323 281 147 332 406 278 117 84 266 221 2 15 129 105 137 20 13 223 47 285 265 238 319 171 415 384 232 12 155 429 177 216 74 97 114 56 16 144 377 316 107 35 100 283 200 214 272 76 279 17 5 350 Coefficient Stage C l u s t e r 1st Appears Cluster 1 Cluster 2 Next Stage 169 291 78 63 141 62 64 212 119 209 198 186 336 171 231 103 105 145 124 98 181 108 144 134 252 61 171 201 150 199 154 248 84 163 246 53 244 221 189 199 150 169 176 257 * * * * * * H I E R A R C H I C A L 136 C L U S T E R A N A L Y S I S * * * * * * Agglomeration Schedule using Ward Method (CONT.) Clusters Stage Cluster1 Combined Cluster2 Stage C l u s t e r 1st Appears Coefficient Cluster 1 Cluster 2 Next Stage 137 * * * * + * H I E R A R C H I C A L C L U S T E R A N A L Y S I S * " * * * * Agglomeration Schedule using Ward Method ( C O N T . ) Clusters Stage Cluster 1 Combined Cluster 2 Stage C l u s t e r 1st Appears Coefficient Cluster 1 Cluster 2 Next Stage 138 * * * * * * H I E R A R C H I C A L C L U S T E R A N A L Y S I S * * + * * * Agglomeration Schedule using Ward Method (CONT.) Clusters Stage Cluster 1 Stage C l u s t e r 1st Appears Combined Cluster 2 Coefficient Cluster I Cluster 2 Next Stage 139 * * * * * + H I E R A R C H I C A L C L U S T E R A N A L Y S I S * * * * * * Agglomeration Schedule using Ward Method (CONT.) Clusters Stage Cluster 1 Stage Cluster 1st Appears Conibined Cluster 2 Coefficient Cluster 1 Cluster 2 Next Stage * * * * * * H I E R A R C H I C A L 140 C L U S T E R A N A L Y S I S * * * * * * Agglomeration Schedule using Ward Method (CONT.) Clusters Stage Cluster 1 S t a g e Cluster 1st Appears Combined Cluster 2 Coefficient Cluster 1 Cluster 2 Next Stage Agglomeration Schedule using Ward Method (CONT.) Clusters Stage Cluster 1 Stage Cluster 1st Appears Combined Cluster 2 Coefficient Cluster 1 Cluster 2 Next Stage APPENDIX TV: RESULTS FROM NON-HIERARC'XICAL CLUSTER ANALYSIS COMPUTE scalel = (var24u 1 + var24m-1 + var24@2 + var24f-1 + var24i-1 + var24a-1 + var24t-1) /-7 . EXECUTE . COMPUTE scale2 = (var24n-l + var24u-1 + var24c-2 + var24e-2 + var24k-1 + var24j-1) / 6 . EXECUTE COMPUTE scale3 = (var24x-1 + var241-1 + var24y-1) / 3 . EXECUTE . . RECODE var24a -2 var24v-l var24p-1 var24e-2 (1=7) (2=6) (315) ( 5 x 3 ) (6=2) (7=1) var24pln var24e2N . EXECUTE . (4=4) INTO var24a2n var24vln RMV /var24a 3=SMEAN(var24a2n) /var24~-3=S~~AN(var24vln) /var24p 3-SMEAN (var24pln) /var24e-3=~MUW(var24e2n) COMPUTE scale4 = (var24a 3 + var24v 3 + var24h-l + var24i-1 + var24p-3 + var24j-1 + var24b-l + var24b-2) /-8 EXECUTE . COMPUTE scale5 = (var24d-2 + var24d-1 + var24s-1 + var24t-1) / 4 EXECUTE COMPUTE scale6 = (var24r-1 + var24e-1 + var24a-1) / 3 . EXECUTE COMPUTE scale7 = (var24e-3 + var24c-1 + var24g-1) / 3 EXECUTE . COMPUTE scale8 = (var24z-1 + var24b-2 + var24t-1) / 3 . EXECUTE . . . . . . -> QUICK CLUSTER -> scalel scale2 scale3 scale4 scaleS scale6 scale7 scale8 -> /MISSING=LISTWfSE -> /CRITERIA= CLUSTER(3) MXITER(10) CONVERGE(.OZ) -> /INITIAL = (5.60 3.83 3.73 3.90 5.65 5.17 4.14 5.10 -> 6 - 3 0 3.04 5.32 4.44 6.03 6.14 5.92 5.99 -> 5.04 2.51 3.91 3.17 4.11 6.09 5.44 3.27) -> /METHOD=KMEANS (UPDATE ) -> /SAVE CLUSTER -> /PRINT INITIAL ANOVA -> . Initial Cfuster Centers. (Front subcomand INITIAL) Cluster Cluster Convergence achieved due to no oe small distance change. The maximum distance by which any center has changed is -0201 Current iteration is 2 Minimum distance between initial centers is 2.9966 Iteration 1 2 Change in Cluster Centers 1 2 3 .2300 .2554 .2876 .O227 O015 .O304 . F i n a l Cluster Centers. Cluster SCALE5 SCALE6 SCALE7 SCALE8 Analysis of Variance. Variable Cluster MS DF E r r o r MS Number of Cases i n each Cluster. Cluster unweighted cases Missing Valid c a s e s Variable Saved i n t o Working File. QCL-1 (Cluster Number ) weighted cases DF F Prob APPENDIX v: RESULTS FROM DISCRIMTNANT ANALYSIS 147 -> DISCRIMINANT -> / G R O U P S = C ~ U ~ - S (1 3 ) -> / ~ I A B L E S = c o u n s l _ i questd-1 questp-1 counlp 1 anyinf-1 cnsldr-1 cnslph-l -> askphc-1 askdrc-1 srchco-1 anyinf-2 srchco-2-> /ANALYSIS ALL -> /PRIORS SIZE -> /STATISTICS=MEAN STDDEV UNIVE' BOXM COEFF RAW TABLE -> /PLOT=cOMBINED -> /CLASSIE'Y=NONMISSING POOLED MEANSUB . _ _ _ - _ _ - -D I S C R I M I N A N T On groups defined by CLU3-2 A N A L Y S r S Ward Method 412 (Unweighted) cases were processed. O of these were excluded f r o m the analysis. 412 (Unweighted) cases will be used in the analysis. Number of cases by group Number of cases Unweighted Weighted 1 131 131.0 2 155 155.0 3 12 6 126.0 CLU3-2 Total 412 Label 412.0 Group means CLU32 COUNSL-1 QUESTD-1 Total CNS LDR-1 Total - - - - - - - - Total .36893 Group standard deviations Total 2.68352 Total -49155 Total .67619 W i l k s ' Lambda ( U - s t a t i s t i c ) and univariate F-ratio w i t h 2 and 4 0 9 degrees o f freedom variable sR C H C O ~ I ANY I N F 2 SRCHCO 2 Wilkst Lambda - - - - - - - - D I S C R I M I N A N T On groups defined by CLU3-2 Analysis number Direct method: A N A L Y S I S Ward Method 1 a l 1 v a r i a b l e s passing the t o l e r a n c e test a r e rntered. Minimum tolerance level.. .....-.--..-....- 0 0 1 0 0 Canonical Discriminant Functions - 2 Maximum number of functions ............. Minimum c u m u l a t i v e p e r c e n t of variance. .. 1 0 0 . 0 0 Maximum significance of W i l k s ' Lambda .... 1 . 0 0 0 0 Prior probabilities Group Prior Total 1.00000 Label Classification f u n c t i o n coefficients (Fisher's l i n e a r d i s c r i m i n a n t functions) QUESTP-1 COUNLP-1 ANYINF-1 CNS LDR-1 CNSLPH-1 SRCHCOII ANY INF-2 SRCHCO-2 (Constant) - - - - - - - - Canonical Discriminant Fmctions P c t of Fcn Eigenvalue Variance Cum Pct Canonical Corr After Fcn Wilks' Lambda Chi-square df S i g * Marks the 2 canonical discriminant functions remaining in the analysis. Standardized canonical discriminant function coefficients Func COUNS L-1 QUESTD-1 QUESTP 1 COUNLPI~ ANYINF-1 CNS LDR-1 CNS LPH-1 ASKPHC-1 ASKDRC-1 S RCHCO-1 ANY INF-2 SRCHCO-2 1 Func 2 Structure matrix: Pooled within-groups correlations between discriminating variables and canonical discriminant functions (Variables ordered by size of correlation within function) Func 1 COUNLP-1 COUNS L-1 CNSLDR-1 CNS LPH-1 ASKDRC-1 .91063* ,54844* .50514* .39360* -,17195* SRCHCO 1 SRCHCO:~ QUESTP-1 QUESTD-1 ANYINF-2 ANYINF-1 ASKPHC-1 .15115 .14180 -.01669 - .O8271 .19243 .Il166 ,14605 Func 2 -.02081 -.29606 -.17311 02063 ,00617 -. ,61518* .59752* .55676* .45639* .44831* .37886* .15923* * denotes largest absolute correlation between each variable and any discriminant function. Unstandardized canonical discriminant function coefficients Func COUNS L-1 QUESTD-1 QUESTP-1 COUNLP-1 ANYINF 1 CNSLDR:~ CNSLPH-1 ASKPHC-L ASKDRC-1 SRCHCO-1 ANY INF-2 SRCHCO-2 (Constant) f Func 2 Func Group 1 Func 2 Test o f Equality of Group Covariance Matrices Using Box's M The ranks and natural logarithms of determinants printed are those of the group covariance matrices- Group Label 1 2 3 Pooled within-groups covariance matrix Box's M Approximate F 294 -28129 1.80862 Hi-Res C h a r t Rank 12 12 12 12 Log Determinant -7.656397 -4.759309 -7.994058 -5.949245 Degrees of freedom 156, 421944.8 # 6:ALl-groups scatterplot Significance .O000 Classification results Group I Group 2 G r oup 3 - Percent o f "grouped" cases c o r r e c t l y classified: 52.18% Classification processing s m m a r y 412 (Unweighted) cases were processed. O cases were excluded for missing o r out-of-range group codes. 412 (Unweighted) cases were used f o r printed output. -> DISCRIMINANT -> /GROUPS=clu3-2(1 3 ) -> -> -> -> -> -> -> 156 /VARIABLES=var40 hhsize hhi resp-age mar-st-n atlantic quebec o n t a r i o prairies bc /ANALYSIS ALL /PRIORS SIZE /STATISTICS=TABLE / PLOT=COMBINED /CLASSIFY=NONMISSING POOLED MEANSUB . resp-e-n employ-n status-n _ - _ _ - _ - -D I S C R I M I N A N T On groups deiined by CLU3-2 A N A L Y S I S - - - - - - - - Ward Method 428 (Unweighted) cases were processed. 10 of these were excluded from the analysis. O had missing or out-of-range group codes. 10 had at least one missing discriminating variable. 418 (Unweighted) cases will be used in the analysis. Number of cases by group CLU3-2 1 2 3 Total Number of cases Unweighted Weighted 131 131.0 160 160.0 127 127.0 Label - - - - - _ - - D I S C R I M I N A N T On groups defined by CLU3-2 Analysis ntrmber Direct method: A N A L Y S I S - - - - - - - - Ward Method 1 al1 variables passing the tolerance test are entered. Minimum tolerance l e v e l . ................. .O0100 Canonical Discriminant Functions Maximum number of functions.............. Minimum cumulative percent of variance ... Maximum significance of Wilks' Lambda .... 2 100.00 1.0000 Prior probabilities ~roup Total Prior Label 1.00000 The following variable failed the toierance test. Variable Within Groups Variance Tolerance Minimum Tolerance BC Canonical Discriminant Functions Pct of Fcn Eigenvalue Variance C u Pct Canonical After Wilks ' Corr Fcn Lambda Chi-square df Sig * Marks the 2 canonical discriminant functions remaining in the analysis. Standardized canonical discriminant function coefficients Func 1 Func 2 VAR40 HHSIZE HHI RES P-AGE MAR-ST-N RES P E N EMPLOYN STATUSN ATLANTIC QUEBEC ONTARIO PRAIRIES Structure matrix: Pooled within-groups correlations between discriminating variables and canonical discriminant functions (Variables ordered by size of correlation w i t h m function) Func 1 Func 2 STATUS N BHSIZEEMPLOY-N VAR40 BC QUEBEC RE S P - E N ATLANTIC RES P-AGE PRAIRIES MAR ST-N HHI- ONTARIO -.5 0 7 1 1 - -09046 -.19242 ,06904 .08215 .56410* .42790f .32776* .22095* 12090X -. * denotes largest absolute correlation between each variable and any discriminant function. Canonical discriminant functions evaluated at group means (group centroids) Group Hi-Res C h a r t Func 1 Func # 2:AJ.l-groups 2 scatterplot C l a s s i f i c a t i o n results - Group 1 133 Group 2 165 Group 3 130 Percent of "grouped" c a s e s c o r r e c t l y c l a s s i f i e d : 47.66% C l a s s i f i c a t i o n processing summary 428 (Unweighted) cases were processed. O cases were excluded f o r missing or out-of-range group codes. 428 (Unweighted) c a s e s were used for printed o u t p u t . 162 -> DISCRIMINANT -> /GROUPS=clu3_2(T 3 ) -> /VARIABLES=varZ var6b var7 varlOa varlob varlla varllb varlia varlîb -> varl8a varl8b respirat obgyne bowel cancer musculo mental cardio dermatol -> pain blood nutrit neurolog hepatic endocrin genita other var32 var33 var34 -> /ANALYSZS ALL -> /PRIORS SIZE -> /STATISTICS=TABLE -> /PLOT=COMBINED -> /CLXSIFY=NONMISSING POOLED MEANSUB . _ _ _ - - - _ -D I S C R I M I N A N T On groups defined by CLU3-2 A N A L Y S I S - - - - - - - - Ward Method 418 (Unweighted) cases were processed. 143 of these were excluded from the analysis. O had missing or out-of-range group codes. 143 had at l c a s t one missing discriminating variable. 275 (Unweighted) cases will be used in the analysis. Number of cases by group CLU3-2 I Total Number of cases Unweighted Weighted 80 80.0 Label - - - - - - - - D I S C R I M I N A N T On groups defined by CLU3-2 Direct method: A N A L Y S I S - - - - - - - - Ward Method al1 variables passing the tolerance test are entered. Minimum tolerance level .................. .O0100 Canonical Discriminant Functions Maximum number of functions.............. Minimum cumulative percent of variance ... Maximum significance of W i l k s ' Lambda .... 2 100.00 1.0000 Prior probabilities Group Prior Total 1.00000 Label The following 6 variables failed the tolerance test. Variable Within Groups Variance CANCER BLOOD NEUROLOG HEPATIC GENITA OTHER .O00000 .O00000 .O00000 .O00000 .O00000 -168746 Tolerance .O000000 ,0000000 .0000000 ,0000000 .O000000 .O000000 Minimum Toler ance .0000000 .O000000 ,0000000 .0000000 .O000000 .O000000 Canonical Discriminant Functions P c t of Fcn Eigenvalue Variance I* 2* .5200 .O979 84.16 15.84 Cum Pct 84-16 100.00 Canonical Corr .5849 : .2986 : After Fcn Wilks' Lambda Chi-square df Sig 133.401 24.331 48 23 .O000 .3857 O -599239 1 .910829 * Marks the 2 canonical discriminant functions remaining in the analysis. Standardized canonical discriminant function coefficients VAR2 VAR6B VAR7 VARlOA VARlOB vAR11A VARllB VARl 7A VAR17B VARl 8A VAR18B RESPIRAT OBGYNE BOWEL MUSCULO mNTAL CARDI0 DERMATOL PAIN NUTRIT ENDOCRIN VAR32 VAR33 VAR3 4 Structure matrix: Pooled within-groups correlations between discriminating variables and canonical discriminant functions (Variables ordered by size of correlation within function) Func VARllB VAR1 1A VAR18B VÀR7 VAR18A VARl OA RESPIRAT VARl OB VAR32 VAR17A VAR2 VARl7B VAR6B DERMATOL OTHER VAR33 OBGYNE BOWEL MUSCULO VAR3 4 ENDOCRIN NUTRIT PAIN CARDI0 MENTAL Func 1 2 -.10381 .71231* .58442* .42425* 39164* .38719* .27768* ,20167* .18147* -.17111* .16404* .15283* .14600* .O3755 -08592 ,21196 -13845 .O5336 13044 .O6063 -.01880 -. 11442 -13081 -.O9354 -13544 -02211 -.03408 -.23373 .O5470 -. 08324 01609 .O5387 03376 02573 .O1235 -.10136 00336 .36786* .32963* 30401* - .26331* .24644* -.22836* .21459* .19629* .15857* ,12087* .11474* -. 11372* .03917* -. -. -. -. -. -. -. * denotes largest absolute correlation between each variable and any discriminant function, Canonical discriminant functions evaluated at group means (group centroids) Group Hi-Res Chart Func 1 Func 2 # 4:All-groups scatterplot Classification r e s u l t s Group 1 Group 2 Group 3 - Percent of "groupedm cases correctly classified: 52.15% Classification processing summary 418 (Unweighted) cases were processed. O cases were excluded for missing or out-of-range group codes. 418 (Unweighted) cases were used for printed output. APPENDIX VI: RESULTS FROM LOGISTIC REGRESSION -> L O G I S T I C REGRESSION cl1.13-1-2 169 /METHOD-ENTER var4O-1 hhsize-l hhi 1 resp-a-1 mar st-1 resp-e-1 -> -> status-1 atlant-1 quebec-1 ontari-ï prairi-1 bc-1-> /CLASSPLOT -> / C R I T E R I A P I N ( . O S ) POUT(.lO) ITERATE(2O) - employ-1 170 Total number o f cases: 428 (Unweighted) Number of selected cases: 428 Number of unselected cases: O Number of selected cases: 428 Number rejected because of missing data: 130 Number of cases included in the analysis: 298 Dependent Variable Encoding: Original Internai Value 1-00 Value 2.00 O 1 171 Dependent Variable.. CLU3-ld2 Beginning Block Number -2 Log Likelihood O. Initial Log Likelihood Function 409.67284 Constant is included in the model. Beginning Block Number 1. Method: Enter Redundancies in Design Matrix: Variable(s) Entesed on Step Number SMEAN (VAR40) 1.. VAR40 1 HHSIZE-i SMEAN(HHS1ZE) SMEAN (HHI) HHI-1 SMEAN (RESP-AGE) RES P-A-1 SMEAN (MAR-STN) MAR-ST-1 RES PE-1 SMEAN (RESPE-N) SMEAN ( EMPLOYN) LMPLOY-1 STATUS-1 SMEAN ( STATUSN) SMEAN (ATLANTIC) ATLANT-1 QUEBEC-1 SMEAN ( QUEBEC ) ONTARI-1 SMEAN (ONTARIO) PRAIRI-1 SMEAN ( P W R I E S ) Estimation terminated at iteration number 3 because Log Likelihood decreased by less than -01 percent. -2 Log Likelihood Goodness of Fit 392.960 299.322 Chi-Square Mode1 Chi-Square Improvement ;= 16.713 16.713 ci£ Significance 12 12 -1607 ,1607 Classification Table for CLU3-1-2 Observed 1.00 2.00 1 2 Predicted Percent Correct 2-; 45.86% 128 77.58% Overall 63.42% B Variable S.E. Wald df Sig R Exp(B) VAR40 1 HHS IzE-1 HHI-1 RES P A 1 MARST-1 STATUS:~ ATLANT-1 QUEBEC-1 ONTARI-1 PRAIRI-1 Constant Observed Groups and Predicted Probabilities - 20 -- F R 15 I -- E Q u E N C Y 10 -- 5 -2 1 22 2 22 2 22 2 22 2 2 2 222 2 2 22 222222 22 22 22 2222212222 22 12222222212221 22 2 212222222212221222 2 122121222222112212222 2 11211122222111221222222 2 11111111121111211222222 22 1111111112111r2111222222 llllilllllllllllllll1112211122 llll1lllllllllllllll111I1111112 1 1 i T I I I Predic ted L I 1 Prob: O .25 .5 .75 1 Group: 111111111111111111111111111111222222222222222222222222222222 Predicted Probability is of Membership for 2 .O0 Symbols: 1 - 1.00 2 - 2.00 Each Symbol Represents 1.25 Cases. -> LOGISTIC REGRESSION clu3-1-3 -> /METHOD=ENTER var40-1 hhsize-1 hhi-1 resp-a-1 m a o t - 1 -> status-1 atlant-1 quebec-1 ontari-1 prairi-1 bc-l -> /CLASSPLOT -> / C R I T E R I A PIN ( .O5 ) FOUT ( .IO) ITERATE (20) . resp-e-1 employ-1 Total number of cases: 428 (Unweighted) 428 Number of selected cases: Number of unselected cases: O Number of selected cases: 428 Number rejected because of missing data: 165 Number of cases included in the analysis: 263 Dependent Variable Encoding: Original Interna1 Value 1-00 3.00 Value O I 175 Dependent Variable.. CLU3-1-3 Beginning Block Number -2 Log Likelihood I h i t i a l Log Likelihood Function O. 364.5612 Beginning Block Number 1. Method: Enter Redundancies in Design Matrix: Variable ( s ) Entered 1.. VAR40 1 HHSIZE-1 HHI-1 RESP A l on Step Number SMEAN (VAR401 SMEAN (HHSIZE) SMEAN(IM1) SMEAN ( RES P-AGE 1 SMEAN ( MAR-S T-N ) SMEAN (RESP-E-N) SMEAN (EMPLOYN) SMEAN (STATUS-N) SMEAN (ATLANTIC) SMEAN ( QUEBEC1 SMEAN (ONTARIO) SMEAN ( PRAIRIES) Estimation terminated at iteration number 3 because Log Likelihood decreased by less than .O1 percent. -2 Log Likelihood Goodness of Fit 347.150 264.386 chi-Square df Significance lm Mode1 Chi-Square Improvement 17 - 412 17.412 12 12 ,1348 -1348 Classification Table for CLU3-1-3 Predicted Percent Correct Observed 1.00 1 3.00 3 63.16% 63.08% Overall 63-12% Variable S.E. .3163 .1486 ,0555 .O107 -3890 .1342 ,5459 .1834 .5859 .4796 .4449 ,5346 20.9560 RES P-A-1 MAR ST 1 PRAIRIII Constant Wald Sig .O379 1.0883 ,0109 4.2835 .3020 -5614 .8456 .2969 .9167 .O385 .5827 .4537 -5806 -8038 .8933 -3807 ,6559 .7180 .3052 .O617 .O180 .7685 .1986 .1304 4.1559 .O415 Observed Groups and Predicted P r o b a b i l i t i e s I I 1 Predicted 1 I -75 1 Prob: O .25 .5 Group: 111111111111111111111111111111333333333333333333333333333333 P r e d i c t e d P r o b a b i l i t y i s of Membership for 3.00 synibols: 1 - 1 . 0 0 3.00 3 Each Symbol R e p r e s e n t s 1 Case. - -> LOGISTIC REGRESSION ~ 1 ~ 3 - 2 - 3 -> /METAOD=ENTER var40-1 hhsize-1 hhi-1 resp-a-l marst-1 resp-e-1 -> status-1 atlant-l quebec-1 ontari-1 prairi-1 bc-1 employ-1 178 Total number of cases: 428 (Unweighted) N d e r of selected c a s e s : 428 Number of unselected cases: O Number of selected c a s e s : 428 Number rejected because of missing data: 133 Number of cases included in the analysis: 2 9 5 Dependent Variable Encoding: Original Value 2.00 3.00 Interna1 Value O I 179 Dependent Variable.. CLU3-2-3 Beginning Block Number -2 Log Likelihood Initial Log Likelihood function O. 404.7945 * Constant is included in the model, Beginning Block Number 1. Method: Enter Redundancies in Design Matrix: Variable (s) Entered 1.. VAR40-1 HHS IZE-1 HHI-1 RES P-A-I MAR-ST-1 RLso E 1 EMPLOYI~ Estimation terminateci at iteration number 3 because Log Likelihood decreased by less than .O1 percent. -2 Log Likelihood Goociness of Fit 380.170 293.252 Chi-Square Mode1 Chi-Square Improvement 24.624 12 24.624 12 Classification Table for CLU3-2-3 Predicted 2.00 3.00 2 1 3 Observed 2.00 3.00 df Significance 3 Percent Correct 78.79% 40.00% Overall .O167 .O167 61.69% ---------------------Variable 3 180 Variables in the Equation S.E. Wald df ----------------------Sig R ExpW VAR40-1 HHSIZE 1 RES P-E-1 EMPLOY-1 STATUS-1 ATLANT-1 Observed Groups and Predicted P r o b a b i l i t i e s l I 1 Predicted 1 I 1 Prob: O -25 .5 -75 Group: 222222222222222222222222222222333333333333333333333333333333 Predicted Probability - is of Membership for 3-00 Symbols: 2 - 2.00 3 - 3.00 Each Symbol Represents 1.25 Cases. APPENDIX VII: QUESTIONNAIRE CONSyMER MAIL PANEL of Canada Lïmited 77 61oor Stmt West. 12th noor. Toronto. Ontario MSS 3A4 1200, McGlIl College, Suite 1660. Momal (Québec) H3B 4G7 Mukrt Fa- Oear panel rnsmtw, In my S u m m Flexibut you told me tM eiher Um femaIe or the male heaâ of your househoid had taken msdicaüon(s) pnsaibeâ by a dodor h the prsvfousâweke montht. The person bking the medication also very kfndty agrsad to amplete a qusstioM)Ùn about pfusxiptron dnip wage. The purpaa of the questionnaire Ir to find out what Canadians krow and want to krow abut prssafption dniqs; and w h l sou^ are uscd to obtain th& Information. As I menüoned in the Summn ~exibus,r futttier p r p s e k to halp a postqnduets univenity dodent ampiete a rnastefs degree. When answœfng thb qu&onnain, piaw think onty about the prwaipüon th& was m o d mcsntiy fillad for you. and answer the quedons about thrt d m g only. If, by any chance. you hacl m o n than one prescription fiIIcd at Vie same tirne. plcase anthe quesüoru about only one of them. whichever one you wish to ctiooje. W o n d# you h w e pmsalptlonfillad? Withh the past week .......................... 1 -2wea!aago .................................. 3 -4weekago ....-....-.................*--..* O 1 2 montfit ago .....,,,.............-.m..--... O 3 6 monttu ago .....*.............*............ 0 7 11 months ago O 1 yaar ago 0 Mors than one year aga U - - - .........*.................... .......................................... ..................... Was this plbJaipti0n a refill of ?n old prescription or a new prescription 0.0. a dnig yau had never taken befon)? Am you taking mis medication noYes...............O No ................ 4 SKIP TO QU.4b a For how long have you been taking this medication? {PLEASE "Xn ONE BOX UNDER QU.&) Qu,Qa H m long petn taking L e s titan a week ............................--.a 1 2 weeks.-..................................... O 3 - 4we- ......................................... 0 1 2 montht.................................... a 3 6 manths................................... O 7 11 m o m O 1 year O ivlore than one year 3 . - . . .................................. ................................................ ............................ For how long did you take this medicaîlon? (PLEASE Qu.rlb HOWlong took for a O O O O O O ONE BOX UNOER QU.4b) Whut &bas t h e nama of the medlc&on you wem presuiôcd? (PLEASE WRltE DOWN THE DRUG NAME SHOWN ON THE LABEL OF YOUR BOITLE OR BOX. IF YOU CANT REMEMBER, PLEASE REFER TO THE B0lTl.E OR BOX, IF AVAiiA8i.E. TO ANSWER THIS QUESTION). For Mat wndiüoMllness was th& dntg pmsufbd? 1s th& condition a chronic or a short-term illness? (PLEASE @X"ONE BOX) .................... 0 ................................... ,.O Chmnic ilInes............, . . Short-term iltness Other (PLEASEDESCRIBE) Overat!, how knowlwaable do you feel you am about the drug p u were p M b e d ? (PLEASE ClRCLE ONE NUMBER BELOW) 7. - ~ o at ail edaeable 1 2 Extrernely know(edaeabI8 3 4 5 7 6 How knawledgeable do you feel you are about ... (PLEASE ClRCLE ONE NUMBER FOR EACH S T A f E M W T 8. BELOW) Not at ail ~owlodoea blq hou many tfmes psr day to take or use the medication 1 2 how much medîlcab'onto trke or use each tfms ................1 2 when the medication should be taken or used 1 2 how to take or use the medicaîjon ..............-....-.-.......-..... 1 2 ~ s i â e ~ u f t h s r n d l ~ o...n.................. 1 2 2 posdble conmûs wfth mer madications 1 whd not to eat, d m or do whils Wng. or wing the madlcatim ........-...........-............-........1 2 othw m e d i d a n t üta! can be usad to tnat the same ~ W "*.-" o ~ 1 2 athœ non-dmg trwtmenîs thaî can be used to üeat the srme ~ o n l i O such n ~as hameopoüiy, acuppinawd,etc. 1 2 wîtut the madkatron rchialiy does .... 1 2 hou much the medication cwts . . 1 2 Not appR G&!Q O ..... .................. O O O ................................ O O ........................... ...... ..........,........ ...................... ~~..........~.............-....... ....................... . . ............... . . . . . o n . . . . . . . . . . . . O O 4 4 3 3 3 4 5 5 5 6 8 8 O 7 7 7 O O Nw WOU# liks you to te1 ma what information. if any,you rsosived about your p-paon dnig from the dodor rrhD preyibed yow mdicstlan. For each of Fe items klow, plùidicR. whethu Viis information was offaced to you wdhovt having to ask about it, wt~etherR was givtn to you onty aRer you asked about R, or whether you weru not gken any informationat ail. (PLEASE UX" THE APPROPRIATE BOXES UNOER aU.9a) 90) 9u.91 Told G M without iRef gsIng &@J How many tîmes per day to take or use îhe msdiwüm .............................................. O How much madicatlon to taks or use each time......O When the mudication should be taken or used ....... Not given O O D Hawtotaksot~tnemedicaîion .....OO P-e side atrscb of the medication ................... CI PassiMe conflidrr mth oüter medications................ U [3 What not to esaf drink or do while taking or using the rnedldon U U m e r msdications that can be used ta mat the sams condition/illness........................................ O Othw non-dnrg tmaûnents that can be rssed to tmat the same conditiontillness, such as homeopathy, acupuncture, etc. .-. .............. a Whcitthemcdi~onactualiydoes......................... 0 fJ Haw much the meâicltion costs O CI Other bifomiation m h r s d (PLEASE DESCRIBE) O ........................ ........................................... ..................... . .... 9b) 100) a a a Not ippb O a O a a O 0 O O O CI O O O Cl I nrould a& liks you to tell me what information, if any, you received about- your pnscrlptiondnig from the phannadst who fitled your prrs#lption. For each of the rtems above, please indiwhether thb information was ofimed io yau wtthout haïfng ta ask about it, Weti~ertt was g h n to you onIy aibr you asked about it, or wtiether you wem not given any irrfomation Pt aI1. (PLEASE THE APPROPRlATE BOXES UNOER QUAb) fi Did you racdve any handwrinen w prlnted infamation about the h g from the dodor who prrsdbed the AS MANY BOXES AS APPLYf mediaüon? (PUASE Qu.iOa ............. TF .................... Yes handwrflten infornation Yw prlnted information O No dld not mceive any written or printed info-on ................... 0 -. O 1Ob) 4 bid you raceive any handwrftten or pfinted information about the drug from the phumacist who tllied the pmscziptlon? (PLEASE AS M M AS BOXES A3 APPLyI Qu.lOb -B- a cl h 184 17a) DM you n a i v e any handwrftten or pfinted information about your cond'tionfillneSS fmm the dodor who -kd the medicéition? (PtEASE "X" ASMANY BOXES AS APPLY) Q!sQ Qu.173 QQGm Y e s - Handmitten information ............ Yes - Pfinted information....................a Phamam 0 - N o Did not receive any m e n or printed infornation ................... O 17b) 18s) 0 -- How siltidled niws you with information the doctor gave you about your wndition/itiness? (PLEASE T ONE =X) Ph- Doaor .........,........,... ..13 .........-.....-.....-................... O .................. O Very satistied Quito saisfiecl Not very satisfied Not at al1 saüsfied 18b) A DM you nceivs any handwntten or printed information about your c o n d i i ~ ~ l l n e from s s the phamadst who filled the pm.ptfon? (PtEASE "X" ASMANVAsBOXESASAPPLY) 0 [=I a 0 How How wem p u witn information the phumacist gave p u about yoor conditfoMifncssi, (PUEAS€ O X " ONE BOX) n g the information p u wem-given by the doctor or phsrmacirt. did you ohlon information ab+ the condiùon/niness for which you a m taking medication h m any dher sources, sudi as from a drug Company, fnends or farnily, magazine or newspaper artfdes, or m e r h e m pmftssionals you had çontad wiVi? 19. v 20. From which other source(s) did you obtain information about your wndiionlillness? (PLEASE WRlTE iN AU OTHER SOURCES USED) BT SOURCE: 2ND SOURCE: 3RD SOURCE: 21. - WhPt information did you obtain frorn thisRhese source(s)? (PLEASE @XW AS MANY BOXES AS APPLY) . . ........ 0 General dcsaipüon of the condMon/illness............. Dewfption of syrnptoms nomally experienced by patients .....0 Information about different dnig trements ..............+.....,....... Information about non-drug tnatments such as homeopaîhy, aarpundure. etc. ..............................................[3 Changes in diet, exercise, etc. to be made ............................. [3 M e r (PLEASE DESCRIBE) ..O 22 What m e r infomaüon, if any, would you I i b to receive about your condition/inneSS? 23. Now I would like you ta tell me M a t you would do if you saw information about a new prescription drug (1.e. a U n i 0 thaî you didn't know about befon) to t n a t the wndih'on/illness you are, or were. suffedng fmm. Plea~earde a number on t :chof the scales to indicate how Iikely you would bc to ,.. Not at al1 €xtremtly W Y uk a dodor about üie drug 1 aska phatmacist about the dmg...................................................... 1 iind out mom irrfomation about the dnig on your own 1 ask a dodor to pmsaibe the drug for you ........................................ 1 wait for more infomatfon lo becorne availabie about the d ~ ............................................................................... q 1 pay no attention to iî........................................................................ 1 ............................................................. ..................... 2 2 2 2 2 2 3 4 4 4 4 5 S S 5 6 6 3 3 4 4 5 5 6 6 3 3 3 8 6 w 7 7 7 7 f 7 How satisffed were you with infomation the doctor gave you about your prescription medication? ( P M E "XW ONE80X) - Qu.llb. PhannaR pouor Very satisfied ..................................... O Quite satlsfied ...,................... ............ O a Nat very satlsfied ............................. Not at al1 satislied 0 ............................... O H w saWied wem you with information the pharmacist gave you about your prsscrlption madication? (PLEASE "X" ONE BOX) Exduâing the infonpation you wem ghren by the doclor or phamaast, dki you obtain information about your pmsai on medicpaon fmm any mer souras. such as from the Company who makes the drug. Mends or family, mag$Pe ar n-pr arüdes. or orner heaith pmfessioripls you had contact with? Fmm which ather sovcbs dM you obtain information about p u r ptes#Iption mcdication? (PLEASE W R ï E IN ALL OTHER SOURCES USED) 13T SOURCE: 2ND SOURCE: 3 m aomcE: What inlomiation did you obtain from WisRheso source(s)? (PLEASEUX" AS MANY BOXES AS APPLY) How mmy Urnes par day to take or uta the rndcation.................. How much medication to take or use eadi time ............................. O Whsn the medication shouM be taksn or useci .........-..................... How to take or use the medicaüon ....................................-..... 0 PoHbls side effet% of the medication .......................................... a Possible confiidt with other medications .............................-....... 13 W?m! not to eat. drink or do while taking- or wing the msdicotion................................................................................... a 0 t h medicafons ~ th& can be used to mat the same condition/ n iünOthef non-dnrg trsatments that can be used ta treat the sama candillonmlness, such as horneopathy, acupuncture. etc, 0 W h l the msdication actualiy does O How much the msdldon costs a OVisr (PLEASE DESCRIBE) ........ 0 ....................................................................................... ... ............................................ ..................................................... What m e r infomation, if any, would you Iike to receive about your pe rscp oirtn medication? On P *lacd subjed. 1 woufd like you to tell me what information. ifany, you received about your conditian/illness frum the d o d w who pricsaibed your medication. For each of the items below. please indicate whether t h e infomiaüun was offerad to p u m u t having to ask ahut it, whether it was given ta you only aRer you asked about it, or whether p u wem not qfven any i n f ~ r m ~ oabout n iî at ail. (PLEASE "XW THE APQROPRlAm BOXES UNDER QU.1Sâ) Told wiaiout pskinq ....,,. ................................. General description of the condltion/illness 0 ûesalption of symptoms nomalfy experlenc-nd by patients O Information about differsnt drug treatments......O Information about non-drug treatments wch as homeapathy, acupundum, etc O Changes in dia. axercise, etc.to be made .......U m e r ( P W E OEsCRIBE) ........... Giveri aRar ask'nq Q- G i aRn as- givm Not Not apoli- Told wïthout O Ij 0 U a O O 0 ff D O i3 0 O a O O O C I would a h fike you to tell me what information, if any, you mcehred about. your conditionAllness fmm the phatmadst who fflled your medication. For each of the Rems above, please fndicate whether this infurmationwas offsrad to you without havïng to ask about il, whether it was given to you only aiter you asked about it or whether you were nOt gbm any infornation about it at all. ( P U E THE APPROPRUSTE BOXES UNDER QU.lôb) ( O n ] Nol appti- G@S n O o 0 Not givcri U n O I 0 0 A 3 a I Q a 186 24. For each datement below, pleass &de one number to show how rnuch you agw or disagree with it. disaaree I usualh as15 the dodctr westions about the dnrg(s) -- a b e d at the time of my medical visit ................... 1 It is helphil to ask my Men& or farnily questions about the drug(s) I am taking....................................... 1 always provides me with infomation about the medication he or sbe gives me .................... 1 The pharma& The company who makes the drug should tell me wtmt f neeû to ltnow about my medication ....,...--..,.....1 My dodor is generaRy open to questions about the d r u ~ ( s )he w she prrsciibes ......................................1 When them is mors than m e medication to ?mat my condition, I should be told a h u t eadi one ............. 1 I uswBy ask the phannacist questions about the dnig(s) when I am having my prexrfption(s) flled .......1 lt b batsr to miy l e s on dodon and mors on your omi cornmon sensa when 1 cornes to ming for yow body - . ..................................... ........................ 1 f oRsn Uks to get irrhmüon about my medicaion(s) f m book and 0th- m e n matsrials ........................ 1 I dont think dodon knaw anaugh about the âmgs they prescribe ............................ -..-..............1 R i e n is not enough prfvay at the phamiacy counter to ask quesiions about the medication 1 haw been prrscribed.................................................. 1 I f d I knuw mors about rny medication than do ather people who toks the same medication................1 I feei M Mabut taWng dnigs when I am knowledgeable about them...-.-....-..-.......-.................. 1 Informationabout my medication b tao hard for me to undentand .............-..~....~.............~.............. 1 Rsmernbefingto taka my medication is oRen dimaitt for me .....................................................1 Them is no need to ask questions about @ -oni dnigs if you tmst the dodor ......................1 I feef I am m o n ccincerned about my health than am other peopie my age ............................................. 1 The doctor ahvays provides me with information about the medication he or she ptoscribes for me ....... 1 D N companies ~ ought to inform consumers about Malth issues and medications................................... 1 1 wuit infornation abut rny -ption dmg(s) so 1 can ddmine if the rndcaüon is worlong or not ...... 1 I feel I dont know enough about rny medication to make infomed choices about which medication I should take........................................... 1.. it's always M e r to seek pmfessional help than to t f yto treat younen ...............*..........'...-.-....--....... 1 1 like to know as much as I GUI about the medication Vie dodor prwafbes for me ......................1 l feui I know mors about my condition Vian do mer people experiendng the same heaHh condition as me ............................................................1 I fwl I know where to find al1 the infornation ......................................... I need on my m e d i ~ o n 1 1 want tnfonnation about my prssaiption drug(s) so I a n decici8 if I should take the mecfication............ 1 rather have the dodor make the dedfon Cornpletefy I WOU# about my treatment Vian for him or her to give me a whole lot of cltoices............................................ 1 2 3 4 5 6 7 When them is more than one medication to treat my andiion. I shouM be ôtlowed to c h o s e wbich madication 1 want to take ................................... 1 2 3 4 5 6 7 The dodor uses wrds I dont understand wtien tclng me about the dmg helshe is preseribing............ 1 2 3 4 5 6 7 It wuld be hcipful if the dactor pmvided written infomaüon about the dnrg(s) halshe presatbcs .......... 1 2 3 4 5 '6 7 fhe pitmacU b tbo for away behind the caunter for me to ask queafaru about the drug(s) presuibed........ 1 2 3 4 5 8 7 it woulj be easler to ask the doctor questions if I though! of s o m quedons and wrote them domi Wria rny appointment 2 3 4 5 6 7 .........-.....-.................. ...1 25, Cornpletely 4QSS dlsaaree Have yau cwr asked a dodor about a pmsdption drug you heard or read about? ............... ................ O --b Yes No SKlP 10 QU.29 26. What wu the name o f the medication you aslred the dodor ahut? 27. What condition was thb medidon intended ta treat? 28. Did the dodor preuri'bethis medidon for you? 29. Have you evef asked a phanaart if there is a %enerkquivalent, or Qieaper substituts. avalable for a dnig a dodor prescrlbed for you? Yes............... O No ................U - 30. Has a phamacid ever suggested a generic equivalent. or deaper suMlute. 10 you insîead of the brand a d0ct0r pnscribed for you? Yes...............a N o ................Cl 31. Dfd you buy the generic, or dieaper substitute. suggested by your pharmacist? 32 About how many tirnes in the past year have you visited a dodot? 34. Ars you coverod by a drug plan that pays for your presaipüon merlkation? SKlP TO QU.32 - ..............a No ........................... 4 SKlP TO QU.37a Yes in part Yes in full ................D - 35. 1s this a gwernment plan or a prfvate hem plan (kg. from your employer)? .............. +SKlP 10 QU.37a 80th........................O Govemment Private plan ............... 36. Whidi form of payment dues your private plan use? - Card at pharmacy........... .............~............................. O Pay and reimbursed.................................................... CI Other (PLEASEDESCRISE) .U 37a) each of the sources listecl bclow in cornmunicating dnigs. On a a l e of 1 to 7, with '1' being 'not at aû klievabtenand T being infomiation to you about p-püon 'ex!mmdy bellevable'. plertse rate sach of the following sources in temis of ils believability in cornrnunicating informationto you about prescription medicaüons. (PLEASE ClRCLE ONE NUMBER UNDER QU.37r FOR EACH SOURCE) Now I would Iike p u to tell me how believable you find 6 7 7 7 Television prograrns Talking to a dodor Talking to a phamaast 6 7 AGovemment Heatth Department 6 6 1 2 3 4 5 1 1 1 2 2 2 3 3 3 11 2 3 4 4 4 5 5 5 6 8 6 7 7 7 4 S 6 71 A 37b) Using the same scak, please rate each of the sources in t e m of its bdievabiüty in communicaüng information to you about conditionslillncses. (PLEASE ClRCLE ONE NUMBER UNDER QU.37ü FOR EACH SOURCE) 38. Whkh do you think W the best source of information about pnrcription dmgs? 39. Wch do yau think is the b.st s o u m of information about heaith conditions or illnesses? 4û. Am you ... (PLEASE 'X" THE APPROPRIATE BOX) a The male head of howehoM .............. The female head of household........... THANK YOU VUW MUCH FOR TAKlNG THE TIME TO F i L i IN THIS QUESflONNAlRE! YOUR CONTRlBUnON T0 THIS PROJECT IS GREATLY APPRECIATED. IMAGE EVALUATION TEST TARGET (QA-3)