A mixed model approach to estimate the survivor average causal effect in cluster‐randomized trials

Author:

Wang Wei1ORCID,Tong Guangyu234ORCID,Hirani Shashivadan P.5,Newman Stanton P.56,Halpern Scott D.17,Small Dylan S.8ORCID,Li Fan34ORCID,Harhay Michael O.17ORCID

Affiliation:

1. Clinical Trials Methods and Outcomes Lab, Palliative and Advanced Illness Research (PAIR) Center Perelman School of Medicine, University of Pennsylvania Philadelphia PA USA

2. Department of Internal Medicine Yale School of Medicine New Haven CT USA

3. Department of Biostatistics Yale School of Public Health New Haven CT USA

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

5. School of Health Sciences City University London London UK

6. Division of Medicine University College London London UK

7. Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine University of Pennsylvania Philadelphia PA USA

8. Department of Statistics and Data Science The Wharton School, University of Pennsylvania Philadelphia PA USA

Abstract

In many medical studies, the outcome measure (such as quality of life, QOL) for some study participants becomes informatively truncated (censored, missing, or unobserved) due to death or other forms of dropout, creating a nonignorable missing data problem. In such cases, the use of a composite outcome or imputation methods that fill in unmeasurable QOL values for those who died rely on strong and untestable assumptions and may be conceptually unappealing to certain stakeholders when estimating a treatment effect. The survivor average causal effect (SACE) is an alternative causal estimand that surmounts some of these issues. While principal stratification has been applied to estimate the SACE in individually randomized trials, methods for estimating the SACE in cluster‐randomized trials are currently limited. To address this gap, we develop a mixed model approach along with an expectation–maximization algorithm to estimate the SACE in cluster‐randomized trials. We model the continuous outcome measure with a random intercept to account for intracluster correlations due to cluster‐level randomization, and model the principal strata membership both with and without a random intercept. In simulations, we compare the performance of our approaches with an existing fixed‐effects approach to illustrate the importance of accounting for clustering in cluster‐randomized trials. The methodology is then illustrated using a cluster‐randomized trial of telecare and assistive technology on health‐related QOL in the elderly.

Funder

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Statistics and Probability,Epidemiology

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