Department of Biostatistics, Yale University School of Public Health, New Haven, Connecticut, USA.
Yale Center for Analytical Sciences, Yale University, New Haven, Connecticut, USA.
Stat Med. 2022 Feb 20;41(4):645-664. doi: 10.1002/sim.9284. Epub 2022 Jan 2.
Motivated by a suicide prevention trial with hierarchical treatment allocation (cluster-level and individual-level treatments), we address the sample size requirements for testing the treatment effects as well as their interaction. We assume a linear mixed model, within which two types of treatment effect estimands (controlled effect and marginal effect) are defined. For each null hypothesis corresponding to an estimand, we derive sample size formulas based on large-sample z-approximation, and provide finite-sample modifications based on a t-approximation. We relax the equal cluster size assumption and express the sample size formulas as functions of the mean and coefficient of variation of cluster sizes. We show that the sample size requirement for testing the controlled effect of the cluster-level treatment is more sensitive to cluster size variability than that for testing the controlled effect of the individual-level treatment; the same observation holds for testing the marginal effects. In addition, we show that the sample size for testing the interaction effect is proportional to that for testing the controlled or the marginal effect of the individual-level treatment. We conduct extensive simulations to validate the proposed sample size formulas, and find the empirical power agrees well with the predicted power for each test. Furthermore, the t-approximations often provide better control of type I error rate with a small number of clusters. Finally, we illustrate our sample size formulas to design the motivating suicide prevention factorial trial. The proposed methods are implemented in the R package H2x2Factorial.
受一项具有层级治疗分配(群组水平和个体水平治疗)的自杀预防试验的启发,我们解决了用于检验治疗效果及其交互作用的样本量要求。我们假设了一个线性混合模型,其中定义了两种类型的治疗效果估计量(受控效果和边缘效果)。对于每个对应于估计量的零假设,我们基于大样本 z-逼近推导出样本量公式,并基于 t-逼近提供有限样本修正。我们放宽了相等群组大小的假设,并将样本量公式表示为群组大小均值和变异系数的函数。我们表明,检验群组水平治疗的受控效果所需的样本量要求比检验个体水平治疗的受控效果对群组大小变异性更为敏感;对于检验边缘效果,也有同样的观察结果。此外,我们表明,检验交互作用效果所需的样本量与检验个体水平治疗的受控或边缘效果所需的样本量成正比。我们进行了广泛的模拟来验证所提出的样本量公式,发现每个检验的经验功效与预测功效非常吻合。此外,t-逼近通常可以在少量群组的情况下更好地控制第一类错误率。最后,我们使用所提出的样本量公式来说明激励性自杀预防析因试验的设计。所提出的方法在 R 包 H2x2Factorial 中实现。