Office of Disease Prevention, National Institutes of Health, Bethesda, Maryland, USA.
Department of Biostatistics, Yale School of Public Health, New Haven, Connecticut, USA.
Stat Med. 2024 Nov 10;43(25):4796-4818. doi: 10.1002/sim.10206. Epub 2024 Sep 3.
Many individually randomized group treatment (IRGT) trials randomly assign individuals to study arms but deliver treatments via shared agents, such as therapists, surgeons, or trainers. Post-randomization interactions induce correlations in outcome measures between participants sharing the same agent. Agents can be nested in or crossed with trial arm, and participants may interact with a single agent or with multiple agents. These complications have led to ambiguity in choice of models but there have been no systematic efforts to identify appropriate analytic models for these study designs. To address this gap, we undertook a simulation study to examine the performance of candidate analytic models in the presence of complex clustering arising from multiple membership, single membership, and single agent settings, in both nested and crossed designs and for a continuous outcome. With nested designs, substantial type I error rate inflation was observed when analytic models did not account for multiple membership and when analytic model weights characterizing the association with multiple agents did not match the data generating mechanism. Conversely, analytic models for crossed designs generally maintained nominal type I error rates unless there was notable imbalance in the number of participants that interact with each agent.
许多个体随机分组治疗(IRGT)试验随机将个体分配到研究组,但通过共享代理(如治疗师、外科医生或培训师)提供治疗。随机分组后,参与者之间的交互作用会导致同一代理的结果测量之间存在相关性。代理可以嵌套在试验臂内或与试验臂交叉,参与者可以与单个代理或多个代理交互。这些并发症导致模型选择存在歧义,但尚未有系统的努力来为这些研究设计确定适当的分析模型。为了解决这一差距,我们进行了一项模拟研究,以检查候选分析模型在存在复杂聚类的情况下的性能,这些聚类源自于多个成员、单个成员和单个代理设置,包括嵌套和交叉设计以及连续结果。对于嵌套设计,当分析模型没有考虑到多个成员,并且分析模型权重描述与多个代理的关联与数据生成机制不匹配时,观察到大量的第一类错误率膨胀。相反,对于交叉设计的分析模型通常保持名义上的第一类错误率,除非与每个代理交互的参与者数量存在明显不平衡。