Predictors of attrition during acute pharmacotherapy of psychotic depression in a clinical trial

Little is known about factors that contribute to attrition in clinical trials of the pharmacotherapy of psychotic depression. The purpose of this study was to identify factors associated with attrition during acute pharmacotherapy in the Study of the Pharmacotherapy of Psychotic Depression II (STOP-PD II) clinical trial. Sociodemographic and clinical variables were assessed at baseline in 269 men and women, aged 18-85 years, who were treated with up to 12 weeks of open-label sertraline plus olanzapine. Univariate analyses examined the association of baseline variables with overall non-completion, as well as reasons for non-completion. Logistic regression was used to model the relationship of the significant univariate predictors with non-completion and its reasons. Seventy-four (27.5 %) participants did not complete the acute treatment phase of STOP-PD II. Male gender, younger age, inpatient status, higher Clinical Global Impression (CGI) severity of illness, and higher severity of psychomotor disturbance were associated with non-completion in univariate analyses. In regression models, higher CGI severity of illness score was the only significant independent predictor of non-completion, explained by withdrawal of consent. Our findings have implications for the retention of persons with psychotic depression in clinical trials.

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Publication Details

Journal
Psychiatry Research
Published
2024-09-12
DOI
https://doi.org/10.1016/j.psychres.2024.116192
Citations
1
Primary Topic
Schizophrenia research and treatment
Type
article
Field-Weighted Citation Impact
0.39

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article

Predictors of attrition during acute pharmacotherapy of psychotic depression in a clinical trial

Patricia Marino, Alastair J. Flint, Nicholas H. Neufeld, Benoit H. Mulsant et al.
1 citations
Psychiatry Research
Schizophrenia research and treatment
0.39
article

Predictors of attrition during acute pharmacotherapy of psychotic depression in a clinical trial

Patricia Marino, Alastair J. Flint, Nicholas H. Neufeld, Benoit H. Mulsant, Kathleen S. Bingham, George S. Alexopoulos, Aristotle N. Voineskos, Barnett S. Meyers, Ryma A Ihaddadene, Anthony J. Rothschild, Ellen M. Whyte
article en
1 citations

Abstract

Little is known about factors that contribute to attrition in clinical trials of the pharmacotherapy of psychotic depression. The purpose of this study was to identify factors associated with attrition during acute pharmacotherapy in the Study of the Pharmacotherapy of Psychotic Depression II (STOP-PD II) clinical trial. Sociodemographic and clinical variables were assessed at baseline in 269 men and women, aged 18-85 years, who were treated with up to 12 weeks of open-label sertraline plus olanzapine. Univariate analyses examined the association of baseline variables with overall non-completion, as well as reasons for non-completion. Logistic regression was used to model the relationship of the significant univariate predictors with non-completion and its reasons. Seventy-four (27.5 %) participants did not complete the acute treatment phase of STOP-PD II. Male gender, younger age, inpatient status, higher Clinical Global Impression (CGI) severity of illness, and higher severity of psychomotor disturbance were associated with non-completion in univariate analyses. In regression models, higher CGI severity of illness score was the only significant independent predictor of non-completion, explained by withdrawal of consent. Our findings have implications for the retention of persons with psychotic depression in clinical trials.

Psychiatry ResearchVol. 342
UMass Memorial Health Care (US), University Health Network (CA), Centre for Addiction and Mental Health (CA), University of Massachusetts Chan Medical School (US), University of Pittsburgh (US), University of Toronto (CA), Cornell University (US), Weill Cornell Medicine (US)
National Institutes of Health, U.S. Public Health Service, National Institute of Mental Health
Zero hunger
Openalex Percentile: Top 36%
Schizophrenia research and treatment
0.39
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