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首页> 外文期刊>Contemporary Clinical Trials Communications >Audio-digital recordings for surveillance in clinical trials of major depressive disorder
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Audio-digital recordings for surveillance in clinical trials of major depressive disorder

机译:用于重度抑郁症临床试验中监控的音频数字录音

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摘要

Ratings surveillance is used in clinical trials to assure ratings reliability of site-based scores. One surveillance method employs audio-digital recordings of site-based clinician interviews to obtain remote, site-independent scores for assessment of paired scoring concordance and interview quality. We examined the utility of this surveillance strategy using paired site-independent scores derived from recorded site-based Montgomery-Asberg depression rating scale (MADRS) interviews obtained from patients with major depressive disorder (MDD) participating in 5 clinical trials.High correlations were noted between the 3736 paired site-based and site-independent scores across all visits. Some rater “outliers” were identified whose ratings performance improved following remediation. In 3 studies with available outcome data, the blinded remote ratings yielded a high predictive value (91.2%) for replicating treatment response rates.The magnitude of the total MADRS scores affected the directionality of paired scoring deviations in each of the 5 studies. Across all visits, site-based raters scored the more severe MADRS scores (≥30) higher than site-independent raters and the less severe MADRS scores (<20) lower than site-independent raters. Individual MADRS items were similarly affected by the directionality of symptom severity.This analysis affirms the utility of audio-digital recording of site-based interviews as a surveillance strategy for quality assurance (monitoring and remediation). In addition, the high predictive value of blinded remote ratings to replicate site-based treatment outcomes may be useful to affirm primary site-based results when there is a potential of functional unblinding. The use of remote ratings as a primary measure beyond its utility for quality assurance needs further exploration.
机译:在临床试验中使用分级监控来确保基于站点的评分的分级可靠性。一种监视方法是使用基于现场的临床医生访谈的音频数字记录来获取远程的,独立于现场的分数,以评估成对的评分一致性和访谈质量。我们使用配对现场独立配对评分(从参与5项临床试验的重度抑郁症(MDD)患者获得的基于记录的现场蒙哥马利-阿斯伯格抑郁量表(MADRS)访谈中得出)来检验这种监测策略的实用性。所有访问中的3736个配对的基于站点和独立于站点的得分之间的差异。确定了一些评分者“异常值”,其评分性能在修复后有所改善。在3项具有可用结局数据的研究中,盲法远程评估在重复治疗反应率方面产生了较高的预测值(91.2%)。MADRS总评分的幅度影响了5项研究中成对评分偏差的方向性。在所有访问中,基于站点的评分者的MADRS评分(≥30)比不依赖站点的评分者评分更高,而较不依赖MARRS的评分更低(<20)则低于不依赖站点的评分者。 MADRS的各个项目也同样受到症状严重程度的方向性的影响。此分析肯定了现场采访的音频数字记录作为监视质量保证(监视和补救)的策略的实用性。此外,当存在功能失明的潜在可能性时,盲目远程评分对复制基于部位的治疗结果的高预测价值可能有助于确认基于部位的主要结果。除了质量保证的实用性之外,将远程评级用作主要手段还需要进一步探索。

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