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The recording of adverse events from psychological treatments in clinical trials: evidence from a review of NIHR-funded trials

机译:在临床试验中记录来自心理治疗的不良事件:来自NIHR资助的试验回顾的证据

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摘要

Background There is a concern in the literature that harm from interventions is insufficiently documented in clinical trials in general, and in those assessing psychological treatments in particular. A recent decision by a trial steering committee to stop recruitment into a randomized controlled trial (RCT) of a psychological intervention for personality disorder led to an investigation of the recording of harm in trials funded by the National Institute for Health Research (NIHR). Methods The protocols and final reports of all 82 NIHR trials funded between 1995 and 2013 were examined for the reporting of adverse events. These were subdivided by category of intervention. Results None of the psychological intervention trials mentioned the occurrence of an adverse event in their final report. Trials of drug treatments were more likely to mention adverse events in their protocols compared with those using psychological treatments. When adverse events were mentioned, the protocols of psychological interventions relied heavily on severe adverse events guidelines from the National Research Ethics Service (NRES), which were developed for drug rather than psychological interventions and so may not be appropriate for the latter. Conclusions This survey supported the belief that the reporting of adverse events in psychological treatments is weak and the criteria used may not be appropriate. Recommendations are made as to how current practice might be improved.
机译:背景技术文献中关注的一个问题是,通常在临床试验中,尤其是在评估心理治疗的试验中,没有充分记录到干预带来的危害。试验指导委员会最近决定停止招募人格障碍心理干预的随机对照试验(RCT),从而导致对由美国国立卫生研究院(NIHR)资助的试验中的伤害记录进行调查。方法研究了1995年至2013年期间资助的所有82项NIHR试验的方案和最终报告,以报告不良事件。这些按干预类别细分。结果心理干预试验均未在最终报告中提及不良事件的发生。与使用心理疗法的药物相比,药物疗法的试验方案更有可能提及不良事件。当提到不良事件时,心理干预措施在很大程度上依赖于国家研究伦理服务(NRES)的严重不良事件指南,该指南是针对药物而非心理干预而开发的,因此可能不适用于后者。结论这项调查支持以下信念:心理治疗中不良事件的报告很薄弱,所采用的标准可能不合适。就如何改进当前实践提出了建议。

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