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本库首次提交范围:2004-06-23 — 2026-10-14。
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Saturation in G: simple & robust causal inference in cluster randomized trials with informative cluster sizes

簇规模饱和与 g 计算:信息性簇规模下的稳健因果推断

Cluster randomized trials (CRTs) can exhibit informative cluster sizes (ICS) where cluster size is associated with outcomes and/or treatment effects. Under ICS, the individual and cluster-average treatment effects (iATE, cATE) can diverge, and the conventional linear mixed-effects model (LMM) and generalized estimating equation (GEE) with an exchangeable working correlation can produce data-dependent weighted contrasts that are not consistent for either estimand. In these…

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Fixed-Effects Models for Causal Inference in Longitudinal Cluster Randomized and Quasi-Experimental Trials

纵向整群随机与准实验试验中用于因果推断的固定效应模型

This article investigates the model-robustness of fixed-effects models for analyzing a broad class of longitudinal cluster trials (CTs) such as stepped-wedge, parallel-with-baseline and crossover designs, encompassing both randomized (CRTs) and quasi-experimental (CQTs) designs. We clarify a longstanding misconception in biostatistics, demonstrating that fixed-effects models, traditionally perceived as targeting only finite-sample conditional estimands, can effectively…

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Who's Winning? Clarifying Estimands Based on Win Statistics in Cluster Randomized Trials

谁占优势?澄清整群随机试验中基于胜出统计量的估计目标

Treatment effect estimands based on win statistics, including the win ratio, win odds, and win difference are increasingly popular targets for summarizing endpoints in clinical trials. Such win estimands offer an intuitive approach for prioritizing outcomes by clinical importance. The implementation and interpretation of win estimands is complicated in cluster randomized trials (CRTs), where researchers can target fundamentally different estimands on the individual-level or…

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What is estimated in cluster randomized crossover trials with informative sizes? -- A survey of estimands and common estimators

信息性规模下的整群随机交叉试验究竟估计什么:目标量与常用估计量综述

In the analysis of cluster randomized trials (CRTs), previous work has defined two meaningful estimands: the individual-average treatment effect (iATE) and cluster-average treatment effect (cATE) estimand, to address individual and cluster-level hypotheses. In multi-period CRT designs, such as the cluster randomized crossover (CRXO) trial, additional weighted average treatment effect estimands help fully reflect the longitudinal nature of these trial designs, namely the…

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Analysis of Stepped-Wedge Cluster Randomized Trials when treatment effects vary by exposure time or calendar time

处理效应随暴露时间或日历时间变化时的阶梯楔形整群随机试验分析

Stepped-wedge cluster randomized trials (SW-CRTs) are traditionally analyzed with models that assume an immediate and sustained treatment effect. Previous work has shown that making such an assumption in the analysis of SW-CRTs when the true underlying treatment effect varies by exposure time can produce severely misleading estimates. Alternatively, the true underlying treatment effect might vary by calendar time. Comparatively less work has examined treatment effect…

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