Methods for dealing with unequal cluster sizes in cluster randomized trials: A scoping review

被引:6
|
作者
Zhan, Denghuang [1 ,2 ]
Xu, Liang [1 ,2 ]
Ouyang, Yongdong [1 ,2 ]
Sawatzky, Richard [2 ,3 ]
Wong, Hubert [1 ,2 ]
机构
[1] Univ British Columbia, Sch Populat & Publ Hlth, Vancouver, BC, Canada
[2] Univ British Columbia, Ctr Hlth Evaluat & Outcomes Sci, Vancouver, BC, Canada
[3] Trinity Western Univ, Sch Nursing, Langley City, BC, Canada
来源
PLOS ONE | 2021年 / 16卷 / 07期
关键词
RECENT METHODOLOGICAL DEVELOPMENTS; SAMPLE-SIZE; RELATIVE EFFICIENCY; INTRACLUSTER CORRELATION; STATISTICAL-METHODS; BINARY OUTCOMES; CLINICAL-TRIALS; MONTE-CARLO; PERFORMANCE; DESIGN;
D O I
10.1371/journal.pone.0255389
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In a cluster-randomized trial (CRT), the number of participants enrolled often varies across clusters. This variation should be considered during both trial design and data analysis to ensure statistical performance goals are achieved. Most methodological literature on the CRT design has assumed equal cluster sizes. This scoping review focuses on methodology for unequal cluster size CRTs. EMBASE, Medline, Google Scholar, MathSciNet and Web of Science databases were searched to identify English-language articles reporting on methodology for unequal cluster size CRTs published until March 2021. We extracted data on the focus of the paper (power calculation, Type I error etc.), the type of CRT, the type and the range of parameter values investigated (number of clusters, mean cluster size, cluster size coefficient of variation, intra-cluster correlation coefficient, etc.), and the main conclusions. Seventy-nine of 5032 identified papers met the inclusion criteria. Papers primarily focused on the parallel-arm CRT (p-CRT, n = 60, 76%) and the stepped-wedge CRT (n = 14, 18%). Roughly 75% of the papers addressed trial design issues (sample size/power calculation) while 25% focused on analysis considerations (Type I error, bias, etc.). The ranges of parameter values explored varied substantially across different studies. Methods for accounting for unequal cluster sizes in the p-CRT have been investigated extensively for Gaussian and binary outcomes. Synthesizing the findings of these works is difficult as the magnitude of impact of the unequal cluster sizes varies substantially across the combinations and ranges of input parameters. Limited investigations have been done for other combinations of a CRT design by outcome type, particularly methodology involving binary outcomes-the most commonly used type of primary outcome in trials. The paucity of methodological papers outside of the p-CRT with Gaussian or binary outcomes highlights the need for further methodological development to fill the gaps.
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页数:23
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