The nature of the depressive experience in analogue and clinically depressed samples
Introduction
Research on psychological processes in depression often relies on analogue studies of university students. A typical methodology involves administering the Beck Depression Inventory (BDI; Beck et al., 1961, Beck et al., 1979) to a large sample of students. Subsamples of `depressed' and `non-depressed' subjects are then identified and selected for further study based on a somewhat arbitrary cutoff on the BDI. This controversial research practice is based on the assumption that analogue and clinical forms of depression are part of the same continuum (i.e., differences are viewed as quantitative rather than qualitative).
Despite early cautions and criticisms on the use of the BDI for such purposes (Hammen, 1980; Sacco, 1981; Coyne and Gotlib, 1983; Gotlib, 1984), it continues to be a popular approach. Some investigators, sensitive to this issue, have utilized terms such as `dysphoric' (e.g., Clark et al., 1992) and `depressed mood' (e.g., Nolen-Hoeksema et al., 1993) in describing their analogue college samples. Importantly, however, the results obtained in these types of studies are still discussed in the context of psychological models of clinical depression and the presumed analogue–clinical continuum is retained.
The analogue–clinical issue continues to be a contentious one as reflected in several recent exchanges in prominent psychology journals (Vredenburg et al., 1993; Coyne, 1994; Kendall and Flannery-Schroeder, 1995; Tennen et al., 1995aTennen et al., 1995b; Weary et al., 1995; Flett et al., 1997). Following a critical and extensive review of the available evidence, Vredenburg et al. concluded that the use of analogue depressed college students was justified in depression research; yet these authors also underscored the glaring paucity of research that has directly compared analogue and clinically depressed samples. In contrast to the conclusion of Vredenburg et al., the review of Coyne (1994)concluded that the `self-reported distress' in college samples was mild, transient, and qualitatively distinct from a major depressive episode.
This important debate will not begin to be resolved without relevant empirical investigations designed to address this issue, and a call for such research has been a consistent theme in the literature. Flett et al. (1997)recently observed that most of the debate has focused on what they refer to as `phenomenological continuity'. This phenomenological continuity hypothesis states that the nature of the depressive experience differs in intensity (quantitatively), but not in kind (qualitatively), in analogue and clinical samples.
The present study therefore sought to directly compare analogue and clinically depressed samples on the phenomenology of the depressive experience. The most widely accepted definition of `clinical depression' in the literature, at least in North America, is the major depressive episode as described in recent editions of the Diagnostic and Statistical Manual of Mental Disorders (DSM). The current DSM-IV (APA, 1994) provides a detailed description of a major depressive episode including various groups of symptoms (affective, self-perception, cognitive, somatic, suicidal ideation), as well as their required duration (at least two weeks) and consistency (symptoms must be present most of the day, nearly every day). All of this information was used to develop a self-report assessment of the depressive experience with the purpose of gathering detailed information about the severity of all of the symptoms listed for major depressive episode. This measure was used to test the continuity hypothesis. Specifically, symptom patterns will emerge from analogue and clinical samples in this assessment. For example, if college students are more likely to experience distress and self-esteem issues whereas individuals with clinical depression are more likely to experience serious somatic symptoms such as weight loss, then this `qualitative difference' will be captured by the types of symptoms individuals report with the greatest severity. The covariance matrices for these major depression symptom ratings can be compared across samples using several goodness-of-fit indicators. If the two matrices do not provide a close match, this would indicate a qualitatively different nature of depressive experience in analogue and clinical samples, and the phenomenological continuity hypothesis would not be supported. Conversely, if the two matrices do provide a close match, this would provide support for the continuity position.
Section snippets
Participants
The clinical sample was comprised of 101 adult outpatients with a DSM-IV (APA, 1994) diagnosis of major depressive disorder (59 women, 42 men, mean age=44.39 years, SD=14.05). All of the patients were currently experiencing a DSM-IV defined major depressive episode and were non-psychotic. The most common comorbid conditions were dysthymia (29%), panic disorder (21%), and social phobia (17%).
The analogue sample was comprised of 175 undergraduate university students (117 women, 58 men, mean
DDS and BDI comparisons
Comparisons between the analogue and clinical samples on DDS symptom and BDI total scores are presented in Table 1. The clinical sample had significantly higher scores on almost all of the variables compared to the analogue sample except for weekly alcohol intake where the difference was reversed.
There was evidence of impairment in the analogue sample: 57% of the analogue subjects reported at least a moderate level of distress caused by depression symptoms and 50% reported at least a moderate
Discussion
The results of our study support what Flett et al. (1997)have referred to as the `phenomenological continuity' hypothesis in analogue–clinical depression research. In general, the differences observed between our analogue and clinical samples were of a quantitative rather than qualitative nature. A central test in this study involved an analysis of item endorsement of the DSM-IV symptoms of major depressive episode contained in the DDS. This analysis indicated that the symptom structure in the
Acknowledgements
This research was supported by a grant from the Manitoba Health Research Council. Results of this research were presented at the annual conventions of the Association for Advancement of Behavior Therapy, Miami Beach, November 1997, and the Canadian Psychological Association, Toronto, June 1997.
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