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Ratio estimators of intervention effects on event rates in cluster randomized trials

Ma, Xiangmei; Milligan, Paul; Lam, Kwok Fai; Cheung, Yin Bun (2021-01-15)

 
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Ma, Xiangmei
Milligan, Paul
Lam, Kwok Fai
Cheung, Yin Bun
15.01.2021

Statistics in Medicine
doi:10.1002/sim.9226
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Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202111038138

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Peer reviewed
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<p>We consider five asymptotically unbiased estimators of intervention effects on event rates in non-matched and matched-pair cluster randomized trials, including ratio of mean counts (Formula presented.), ratio of mean cluster-level event rates (Formula presented.), ratio of event rates (Formula presented.), double ratio of counts (Formula presented.), and double ratio of event rates (Formula presented.). In the absence of an indirect effect, they all estimate the direct effect of the intervention. Otherwise, (Formula presented.), (Formula presented.) and (Formula presented.) estimate the total effect, which comprises the direct and indirect effects, whereas (Formula presented.) and (Formula presented.) estimate the direct effect only. We derive the conditions under which each estimator is more precise or powerful than its alternatives. To control bias in studies with a small number of clusters, we propose a set of approximately unbiased estimators. We evaluate their properties by simulation and apply the methods to a trial of seasonal malaria chemoprevention. The approximately unbiased estimators are practically unbiased and their confidence intervals usually have coverage probability close to the nominal level; the asymptotically unbiased estimators perform well when the number of clusters is approximately 32 or more per trial arm. Despite its simplicity, (Formula presented.) performs comparably with (Formula presented.) and (Formula presented.) in trials with a large but realistic number of clusters. When the variability of baseline event rate is large and there is no indirect effect, (Formula presented.) and (Formula presented.) tend to offer higher power than (Formula presented.), (Formula presented.) and (Formula presented.). We discuss the implications of these findings to the planning and analysis of cluster randomized trials.</p>
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