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首页> 外文期刊>Psychopharmacology >Magnitude of change with antidepressants and placebo in antidepressant clinical trials using structured, taped and appraised rater interviews (SIGMA-RAPS) compared to trials using traditional semi-structured interviews
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Magnitude of change with antidepressants and placebo in antidepressant clinical trials using structured, taped and appraised rater interviews (SIGMA-RAPS) compared to trials using traditional semi-structured interviews

机译:与使用传统的半结构化访谈进行的结构化,录音化和评估式访谈(SIGMA-RAPS)相比,抗抑郁药和安慰剂在抗抑郁症临床试验中的变化幅度

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摘要

Rationale Although newer interview methods such as Structured Interview Guide for the Montgomery-Asberg Depression Rating Scale (SIGMA; MADRS) with audiotaping and Rater Applied Performance Scale (RAPS) appraisal have been introduced to improve reliability of ratings in antidepressant clinical trials, there is limited evidence that these methods actually improve trial outcome. Objective The objective of this study uis to evaluate outcome in four similarly designed trials of two recently approved antidepressants: two trials randomly used taped SIGMA interviews with RAPS appraisal and two trials used traditional semi-structured MADRS interviews. Methods We reviewed data from patients who were screened (iV=243) and randomized (N= 148), evaluating the magnitude of change with placebo and antidepressants on mean total MADRS score.Results Depressed patients assigned to placebo in trials using taped SIGMA interviews with RAPS appraisal had a significantly larger MADRS change score (M=-11.5+-12.7) compared to patients assigned to placebo in trials using traditional semi-structured interviews (-5.4+-8.9; F(df=1.57)=5.5%p= 0.022). The error variance was also significantly larger in the placebo arm of trials using SIGMA interviews (F=5.43, p=0.023). Depressed patients assigned to antidepressants had similar outcome in all of the four trials. Conclusion The recently suggested modifications in obtaining clinical data in antidepressant trials such as taped SIGMA interviews with RAPS rating appraisals may in fact result in a higher magnitude of placebo response and a lower magnitude of antidepressant-placebo differences compared to the traditional methods of collecting clinical data. These results were unexpected and indicate the necessity to test new methods prospectively, no matter how intuitively sensible they seem, prior to their implementation.
机译:理由尽管引入了新的访谈方法,例如带录音和评估者应用绩效量表(RAPS)的蒙哥马利-阿斯堡抑郁量表(SIGMA; MADRS)的结构化面试指南,以提高抗抑郁药临床试验中评分的可靠性,但仍然存在局限性有证据表明这些方法实际上改善了试验结果。目的本研究的目的是评估两项最近被批准的抗抑郁药的四项类似设计的试验的结果:两项试验随机使用SIGMA录音带进行RAPS评估,两项试验使用传统的半结构化MADRS访谈。方法我们回顾了来自被筛选患者(iV = 243)和随机患者(N = 148)的数据,评估了安慰剂和抗抑郁药对平均MADRS总分的变化幅度。结果在抑郁症患者中,通过录音带SIGMA访谈分配给安慰剂。与使用传统的半结构式访谈的试验中分配给安慰剂的患者相比,RAPS评估的MADRS变化评分(M = -11.5 + -12.7)明显更大(-5.4 + -8.9; F(df = 1.57)= 5.5%p = 0.022)。在使用SIGMA访谈的安慰剂试验组中,误差方差也明显更大(F = 5.43,p = 0.023)。在所有四个试验中,分配给抗抑郁药的抑郁症患者的预后相似。结论与传统的收集临床数据的方法相比,最近建议的在抗抑郁试验中获取临床数据的修改(例如对SIGMA进行RAPS评估的录音采访)实际上可能导致更高的安慰剂反应幅度和更低的抗抑郁剂-安慰剂差异。 。这些结果是出乎意料的,表明在实施之前,有必要对新方法进行前瞻性测试,无论它们看起来多么直观。

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