INFLUENCE OF STUDY DESIGN ON TREATMENT RESPONSE IN ANXIETY DISORDER CLINICAL TRIALS. Issue 12 (5th October 2015)

• Record Type: Journal Article
• Authors: Rutherford, Bret R; Bailey, Veronika S.; Schneier, Franklin R.; Pott, Emily; Brown, Patrick J.; Roose, Steven P.
• Is Part Of: Depression and anxiety. Volume 32:Issue 12(2015:Dec.)
• Page Start: 944
• Page End: 957
• Publication Date: 2015-10-05
• Subjects: antidepressants -- anxiety/anxiety disorder -- clinical trials -- pharmacotherapy -- treatment; Anxiety -- Periodicals; Depression, Mental -- Periodicals; Depression -- Periodicals; Anxiety -- Periodicals; Anxiety Disorders -- Periodicals; 616.8527005
• DOI: 10.1002/da.22433
• Languages: English
• ISSNs: 1091-4269

Abstract

Abstract : Objective: The influence of study design variables and publication year on response to medication and placebo was investigated in clinical trials for social anxiety disorder (SAD), generalized anxiety disorder (GAD), and panic disorder (PD). Method: Hierarchical linear modeling determined whether publication year, treatment assignment (medication vs. placebo), study type (placebo‐controlled or active comparator), study duration, and the number of study visits affected the mean change associated with medication and placebo. Results: In the 66 trials examined, the change associated with both medication and placebo increased over time ( t = 4.23, df = 39, P < .001), but average drug–placebo differences decreased over time ( t = −2.04, df = 46, P = .047). More severe baseline illness was associated with greater drug–placebo differences for serotonin norepinephrine reuptake inhibitors (SNRIs, t = 3.46, df = 106, P = .001) and selective serotonin reuptake inhibitors (SSRI, t = 10.37, df = 106, P < .001). Improvement with medication was significantly greater in active‐comparator studies compared to placebo‐controlled trials ( t = 3.41, df = 39, P = .002). A greater number of study visits was associated with greater symptom improvement in PD trials relative to SAD ( t = 2.83, df = 39, P = .008) and GAD ( t = 2.16, df = 39, P = .037). Conclusions: Placebo response is substantial in SAD, GAD, and PD trials, and its rise over time has been associated with diminished drug–placebo differences. Study design features that influence treatment response in anxiety disorder trials include patient expectancy, frequency of follow‐up visits, and baseline illness severity.