While target trial emulation (TTE) is increasingly used to improve the analysis of non-randomized studies by applying trial design principles, TTE applications to emulate cluster randomized trials (RCTs) have been limited. We performed simulations to prospectively plan data collection of a non-randomized study intended to emulate a village-level cluster RCT when cluster-randomization was infeasible. The planned study will assess the impact of mass distribution of nutritional supplements embedded within an existing immunization program to improve pentavalent vaccination rates among children 12-24 months old in Niger. The design included covariate-constrained random selection of villages for outcome ascertainment at follow-up. Simulations used baseline census data on pentavalent vaccination rates and cluster-level covariates to compare the type I error rate and power of four statistical methods: beta-regression; quasi-binomial regression; inverse probability of treatment weighting (IPTW); and na\"ive Wald test. Of these methods, only IPTW and beta-regression controlled the type I error rate at 0.05, but IPTW yielded poor statistical power. Beta-regression, which showed adequate statistical power, was chosen as our primary analysis. Adopting simulation-guided design principles within TTE can enable robust planning of a group-level non-randomized study emulating a cluster RCT. Lessons from this study also apply to TTE planning of individually-RCTs.
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