Demystifying estimands in cluster-randomised trials

Author:

Kahan Brennan C1ORCID,Blette Bryan S2ORCID,Harhay Michael O13,Halpern Scott D3,Jairath Vipul45,Copas Andrew1,Li Fan67ORCID

Affiliation:

1. MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, UCL, London, UK

2. Department of Biostatistics, Vanderbilt University Medical Center, Nashville, USA

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

4. Department of Medicine, Division of Gastroenterology, Schulich School of Medicine, Western University, London, ON, Canada

5. Department of Epidemiology and Biostatistics, Western University, London, ON, Canada

6. Department of Biostatistics, Yale University School of Public Health, New Haven, CT, USA

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

Abstract

Estimands can help clarify the interpretation of treatment effects and ensure that estimators are aligned with the study's objectives. Cluster-randomised trials require additional attributes to be defined within the estimand compared to individually randomised trials, including whether treatment effects are marginal or cluster-specific, and whether they are participant- or cluster-average. In this paper, we provide formal definitions of estimands encompassing both these attributes using potential outcomes notation and describe differences between them. We then provide an overview of estimators for each estimand, describe their assumptions, and show consistency (i.e. asymptotically unbiased estimation) for a series of analyses based on cluster-level summaries. Then, through a re-analysis of a published cluster-randomised trial, we demonstrate that the choice of both estimand and estimator can affect interpretation. For instance, the estimated odds ratio ranged from 1.38 ( p = 0.17) to 1.83 ( p = 0.03) depending on the target estimand, and for some estimands, the choice of estimator affected the conclusions by leading to smaller treatment effect estimates. We conclude that careful specification of the estimand, along with an appropriate choice of estimator, is essential to ensuring that cluster-randomised trials address the right question.

Funder

Medical Research Council

Patient-Centered Outcomes Research Institute

Publisher

SAGE Publications

Reference53 articles.

1. ICH E9 (R1) addendum on estimands and sensitivity analysis in clinical trials to the guideline on statistical principles for clinical trials. https://www.ema.europa.eu/en/documents/scientific-guideline/ich-e9-r1-addendum-estimands-sensitivity-analysis-clinical-trials-guideline-statistical-principles_en.pdf

2. Eliminating Ambiguous Treatment Effects Using Estimands

3. Estimands in cluster-randomized trials: choosing analyses that answer the right question

4. Estimands in published protocols of randomised trials: urgent improvement needed

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