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Design and conduct of a provider survey to determine a clinically persuasive effect size in planning VA Cooperative Study #590 (Li+)

机译:设计和进行提供者调查以确定在规划VA合作研究#590(Li +)中的临床说服力大小

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摘要

BackgroundThe estimation of an effect size is an important step in designing an adequately powered, feasible clinical trial intended to change clinical practice. During the planning phase of VA Cooperative Study #590, “Double-Blind Placebo-Controlled Study of Lithium for Preventing Repeated Suicidal Self-Directed Violence in Patients with Depression or Bipolar Disorder (Li+),” it was not clear what effect size would be considered large enough to influence prescribing behavior among practicing clinicians.
机译:背景效应量的估计是设计足够动力,可行的临床试验以改变临床实践的重要步骤。在VA合作研究#590“预防抑郁症或双相情感障碍(Li +)患者反复自杀自发性暴力的双盲安慰剂对照锂研究”的计划阶段,目前尚不清楚影响的大小被认为足以影响临床医生的处方行为。

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