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Behavioral versus pharmacological treatments of obsessive compulsive disorder: a meta-analysis
Abstract
The goal of the study was to provide a quantitative analysis of the relative efficacy of all five currently available serotonin reuptake inhibitors (SRIs) and behavior therapy [exposure and response prevention (ERP)] for obsessive compulsive disorder. The relationship between effect size and methodological characteristics was also empirically examined. A search was conducted of several computerized databases covering the dates from 1973 to 1997. Seventy-seven studies were identified, yielding 106 treatment comparisons involving 4641 patients. Effect sizes were analyzed between individual interventions and between intervention class [SRI, ERP or the combined treatment of an SRI with ERP(ERP/SRI)]. Data were analyzed both before and after controlling for methodological variables. The effect size for clomipramine (CMI) was significantly greater than the other SRIs, with the exception of fluoxetine (FLX). CMI was not significantly greater than ERP or ERP/SRI. As a class, ERP was significantly greater than SRIs as a whole. Effect sizes were larger for studies without a control group or random assignment, for self-reported outcome measures, and varied significantly by method of effect size calculation. Year of publication was significantly related to effect size. When controlling for these methodological variables, CMI was not significantly greater than FLX or fluvoxamine (FLV), and ERP was no longer significantly greater than the SRIs as a whole. No significant difference was found between CMI and the other SRIs as a group in head to head trials. No differences in drop-out rates were found. CMI stands out from the other SRIs. This difference is probably not clinically significant enough to warrant first choice treatment, given CMI's greater lethality in overdose. The choice between an SRI or ERP is dominated primarily by the infrequent availability of ERP and to a lesser degree by personal preference. Methodological differences significantly impact effect size.
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“These studies demonstrate that large effect sizes, which were comparable to those obtained in face-to-face therapy [47, 48], can be obtained with minimal therapist contact, although follow-up periods have been relatively shorter than in other outcome studies for OCD that usually report 6-to-12 month follow-up data.”
From Study protocol for a randomised controlled trial of internet-based cognitive-behavioural therapy for obsessive-compulsive disorder (2014) · cites this paper as [47]
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Cognitive-behavioral group therapy in obsessive-compulsive disorder: a clinical trial
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Soomro, G. M. (2012) · Springer eBooks · doi:10.1007/springerreference_223981 · Cited by 32
Metadata
- Authors
- Kobak, K. A., Greist, J. H., Jefferson, J. W., Katzelnick, D. J., & Henk, H. J.
- Venue
- Psychopharmacology
- Published
- 1998-03-23
- Volume
- 136
- Issue
- 3
- Pages
- 205-216
- ISSN
- 0033-3158 (ISSN-L)
- 1432-2072
- OpenAlex
- W2019929334
- Cited by
- 276
- References
- 41
- Citations by year
- 2025: 1 · 2024: 2 · 2023: 2 · 2022: 39 · 2021: 7 · 2020: 1 · 2019: 1 · 2018: 2 · 2017: 5 · 2016: 8 · 2015: 11 · 2014: 8 · 2013: 7 · 2012: 14
- FWCI
- 8.00
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Psychopharmacology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Social Sciences › Psychology › Clinical Psychology › Obsessive-Compulsive Spectrum Disorders
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Anxiety, Depression, Psychometrics, Treatment, Cognitive Processes
- Social Sciences › Psychology › Clinical Psychology › Psychoanalysis and Psychopathology Research
- Keywords
- obsessive-compulsive disorder, serotonin reuptake inhibitors, exposure and response prevention, clomipramine, fluoxetine, fluvoxamine, treatment efficacy, methodological quality, effect size, dropout rates
- MeSH terms
- Behavior Therapy, Humans, Obsessive-Compulsive Disorder, Patient Dropouts, Selective Serotonin Reuptake Inhibitors
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