» Articles » PMID: 20520295

Site Versus Centralized Raters in a Clinical Depression Trial: Impact on Patient Selection and Placebo Response

Overview
Specialty Pharmacology
Date 2010 Jun 4
PMID 20520295
Citations 30
Authors
Affiliations
Soon will be listed here.
Abstract

The use of centralized raters who are remotely linked to sites and interview patients via videoconferencing or teleconferencing has been suggested as a way to improve interrater reliability and interview quality. This study compared the effect of site-based and centralized ratings on patient selection and placebo response in subjects with major depressive disorder. Subjects in a 2-center placebo and active comparator controlled depression trial were interviewed twice at each of 3 time points: baseline, 1-week postbaseline, and end point--once by the site rater and once remotely via videoconference by a centralized rater. Raters were blind to each others' scores. A site-based score of greater than 17 on the 17-item Hamilton Depression Rating Scale (HDRS-17) was required for study entry. When examining all subjects entering the study, site-based raters' HDRS-17 scores were significantly higher than centralized raters' at baseline and postbaseline but not at end point. At baseline, 35% of subjects given an HDRS-17 total score of greater than 17 by a site rater were given an HDRS total score of lower than 17 by a centralized rater and would have been ineligible to enter the study if the centralized rater's score was used to determine study entry. The mean placebo change for site raters (7.52) was significantly greater than the mean placebo change for centralized raters (3.18, P < 0.001). Twenty-eight percent were placebo responders (>50% reduction in HDRS) based on site ratings versus 14% for central ratings (P < 0.001). When examining data only from those subjects whom site and centralized raters agreed were eligible for the study, there was no significant difference in the HDRS-17 scores. Findings suggest that the use of centralized raters could significantly change the study sample in a major depressive disorder trial and lead to significantly less change in mood ratings among those randomized to placebo.

Citing Articles

Current and Emerging Technologies to Address the Placebo Response Challenge in CNS Clinical Trials: Promise, Pitfalls, and Pathways Forward.

Horan W, Sachs G, Velligan D, Davis M, Keefe R, Khin N Innov Clin Neurosci. 2024; 21(1-3):19-30.

PMID: 38495609 PMC: 10941857.


Reliability of Telepsychiatry Assessments Using the Attention-Deficit/Hyperactivity Disorder Rating Scale-IV for Children With Neurodevelopmental Disorders and Their Caregivers: Randomized Feasibility Study.

Kurokawa S, Nomura K, Hosogane N, Nagasawa T, Kawade Y, Matsumoto Y J Med Internet Res. 2024; 26:e51749.

PMID: 38373022 PMC: 10912982. DOI: 10.2196/51749.


Feasibility of remote interviews in assessing disease severity in patients with major depressive disorder: A pilot study.

Sumiyoshi T, Morio Y, Kawashima T, Tachimori H, Hongo S, Kishimoto T Neuropsychopharmacol Rep. 2024; 44(1):149-157.

PMID: 38267023 PMC: 10932799. DOI: 10.1002/npr2.12411.


Initial severity of the Positive and Negative Syndrome Scale (PANSS)-30, its main subscales plus the PANSS-6, and the relationship to subsequent improvement and trial dropout: a pooled participant-level analysis of 18 placebo-controlled risperidone....

Hieronymus F, Correll C, Ostergaard S Transl Psychiatry. 2023; 13(1):191.

PMID: 37286548 PMC: 10247743. DOI: 10.1038/s41398-023-02491-6.


How should we design future mechanistic and/or efficacy clinical trials?.

Fava M Neuropsychopharmacology. 2023; 49(1):197-204.

PMID: 37237086 PMC: 10700333. DOI: 10.1038/s41386-023-01600-9.