Power calculations for cluster randomized trials (CRTs) with right-truncated Poisson-distributed outcomes: a motivating example from a malaria vector control trial

Author:

Mwandigha Lazaro M1ORCID,Fraser Keith J1,Racine-Poon Amy23,Mouksassi Mohamad-Samer3456,Ghani Azra C1

Affiliation:

1. Department of Infectious Disease Epidemiology, MRC Centre for Global Infectious Disease Analysis, Imperial College London, London, UK

2. Department of Statistical Methodology and Consulting, Novartis Pharma AG, Basel, Switzerland

3. Bill & Melinda Gates Foundation, Seattle, WA, USA

4. Department of Strategic Consulting Integrated Drug Development, Certara, Montreal, QC, Canada

5. School of Pharmacy, Department of Pharmaceutical Sciences, Lebanese American University, Byblos, Lebanon

6. Faculty of Pharmacy, Department of Pharmaceutical Sciences, University of Montreal, Montreal, QC, Canada

Abstract

Abstract Background Cluster randomized trials (CRTs) are increasingly used to study the efficacy of interventions targeted at the population level. Formulae exist to calculate sample sizes for CRTs, but they assume that the domain of the outcomes being considered covers the full range of values of the considered distribution. This assumption is frequently incorrect in epidemiological trials in which counts of infection episodes are right-truncated due to practical constraints on the number of times a person can be tested. Methods Motivated by a malaria vector control trial with right-truncated Poisson-distributed outcomes, we investigated the effect of right-truncation on power using Monte Carlo simulations. Results The results demonstrate that the adverse impact of right-truncation is directly proportional to the magnitude of the event rate, λ, with calculations of power being overestimated in instances where right-truncation was not accounted for. The severity of the adverse impact of right-truncation on power was more pronounced when the number of clusters was ≤30 but decreased the further the right-truncation point was from zero. Conclusions Potential right-truncation should always be accounted for in the calculation of sample size requirements at the study design stage.

Funder

Bill and Melinda Gates Foundation

Innovative Vector Control Consortium

UK Medical Research Council and Department for International Development

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Epidemiology

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