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When All Else Fails, Listen to the Patient: A Viewpoint on the Use of Ecological Momentary Assessment in Clinical Trials

机译:当其他所有方法都失败时,请听患者:关于在临床试验中使用生态矩评估的观点

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A major problem in mental health clinical trials, such as depression, is low assay sensitivity in primary outcome measures. This has contributed to clinical trial failures, resulting in the exodus of the pharmaceutical industry from the Central Nervous System space. This reduced assay sensitivity in psychiatry outcome measures stems from inappropriately broad measures, recall bias, and poor interrater reliability. Limitations in the ability of traditional measures to differentiate between the trait versus state-like nature of individual depressive symptoms also contributes to measurement error in clinical trials. In this viewpoint, we argue that ecological momentary assessment (EMA)—frequent, real time, in-the-moment assessments of outcomes, delivered via smartphone—can both overcome these psychometric challenges and reduce clinical trial failures by increasing assay sensitivity and minimizing recall and rater bias. Used in this manner, EMA has the potential to further our understanding of treatment response by allowing for the assessment of dynamic interactions between treatment and distinct symptom response.
机译:心理健康临床试验中的一个主要问题,例如抑郁症,是主要结果指标检测灵敏度低。这导致临床试验失败,导致制药业从中枢神经系统外流。精神病学结果测量中测定灵敏度的降低归因于不适当的广泛测量,召回偏见和较差的间质可靠性。传统措施区分个体抑郁症状的特征和状态性质的能力的局限性也导致临床试验中的测量误差。在这种观点下,我们认为生态瞬时评估(EMA)(通过智能手机进行的频繁,实时,即时的结果即时评估)既可以克服这些心理挑战,又可以通过提高测定灵敏度和最大程度地降低召回率来减少临床试验失败和评估者偏见。通过以这种方式使用,EMA通过评估治疗与不同症状反应之间的动态相互作用,有可能进一步加深我们对治疗反应的了解。

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