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Sample size estimation for stratified individual and cluster randomized trials with binary outcomes

机译:分层个体的样本量估计和与二元成果的分层随机试验

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Individual randomized trials (IRTs) and cluster randomized trials (CRTs) with binary outcomes arise in a variety of settings and are often analyzed by logistic regression (fitted using generalized estimating equations for CRTs). The effect of stratification on the required sample size is less well understood for trials with binary outcomes than for continuous outcomes. We propose easy-to-use methods for sample size estimation for stratified IRTs and CRTs and demonstrate the use of these methods for a tuberculosis prevention CRT currently being planned. For both IRTs and CRTs, we also identify the ratio of the sample size for a stratified trial vs a comparably powered unstratified trial, allowing investigators to evaluate how stratification will affect the required sample size when planning a trial. For CRTs, these can be used when the investigator has estimates of the within-stratum intracluster correlation coefficients (ICCs) or by assuming a common within-stratum ICC. Using these methods, we describe scenarios where stratification may have a practically important impact on the required sample size. We find that in the two-stratum case, for both IRTs and for CRTs with very small cluster sizes, there are unlikely to be plausible scenarios in which an important sample size reduction is achieved when the overall probability of a subject experiencing the event of interest is low. When the probability of events is not small, or when cluster sizes are large, however, there are scenarios where practically important reductions in sample size result from stratification.
机译:在各种环境中出现具有二进制结果的个体随机试验(IRTS)和群集随机试验(CRT),并且通常通过逻辑回归(使用Grensizing估算方程式用于CRT)来分析。对于具有二元成果的试验比连续结果的试验,分层对所需样品尺寸的影响较小。我们提出了用于分层虹膜和CRT的样本量估计的易于使用方法,并证明这些方法用于目前正在计划的结核病预防CRT。对于虹膜和CRT,我们还确定分层试验的样本大小与相对动力的未加价试验的比例,允许调查人员评估规划试验时如何影响所需的样品大小。对于CRT,当研究者具有估计层内插入的相关系数(ICC)或假设层内ICC内,可以使用这些。使用这些方法,我们描述了分层可能对所需的样本大小产生实际重要的影响的情况。我们发现,在两个层面的情况下,对于具有非常小的聚类尺寸的墨水和CRTS,不太可能是合理的情景,其中当经历感兴趣事件的主题的总体概率时,实现了重要的样本量减小低。然而,当事件的概率不小,或者当聚类大小很大时,有方案实际上重要减少样本大小从分层产生。

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