Evaluating analytic models for individually randomized group treatment trials with complex clustering in nested and crossed designs

Author:

Moyer Jonathan C.1ORCID,Li Fan23ORCID,Cook Andrea J.45ORCID,Heagerty Patrick J.5ORCID,Pals Sherri L.6ORCID,Turner Elizabeth L.78ORCID,Wang Rui910ORCID,Zhou Yunji5ORCID,Yu Qilu11ORCID,Wang Xueqi212ORCID,Murray David M.1ORCID

Affiliation:

1. Office of Disease Prevention National Institutes of Health Bethesda Maryland USA

2. Department of Biostatistics Yale School of Public Health New Haven Connecticut USA

3. Center for Methods in Implementation and Prevention Science Yale School of Public Health New Haven Connecticut USA

4. Biostatistics Unit Kaiser Permanente Washington Health Research Institute Seattle Washington USA

5. Department of Biostatistics University of Washington Seattle Washington USA

6. Centers for Disease Control and Prevention Atlanta Georgia USA

7. Department of Biostatistics & Bioinformatics Duke University Durham North Carolina USA

8. Duke Global Health Institute Duke University Durham North Carolina USA

9. Department of Population Medicine Harvard Pilgrim Health Care Institute and Harvard Medical School Boston Massachusetts USA

10. Department of Biostatistics Harvard T. H. Chan School of Public Health Boston Massachusetts USA

11. National Center for Complementary and Integrative Health National Institutes of Health Bethesda Maryland USA

12. Department of Internal Medicine Yale School of Medicine New Haven Connecticut USA

Abstract

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.

Publisher

Wiley

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