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Simple Power and Sample Size Estimation for Non-Randomized Longitudinal Difference in Differences Studies

机译:差异研究中非随机化纵向差异的简单功效和样本大小估计

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摘要

Intervention effects on continuous longitudinal normal outcomes are often estimated in two-arm pre-post interventional studies with b≥1 pre- and k≥1 post-intervention measures using “Difference-in-Differences” (DD) analysis. Although randomization is preferred, non-randomized designs are often necessary due to practical constraints. Power/sample size estimation methods for non-randomized DD designs that incorporate the correlation structure of repeated measures are needed. We derive Generalized Least Squares (GLS) variance estimate of the intervention effect. For the commonly assumed compound symmetry (CS) correlation structure (where the correlation between all repeated measures is a constantρ) this leads to simple power and sample size estimation formulas that can be implemented using pencil and paper. Given a constrained number of total timepoints (T), having as close to possible equal number of pre-and post-intervention timepoints (b=k) achieves greatest power. When planning a study with 7 or less timepoints, given large ρ(ρ≥0.6) in multiple baseline measures (b≥2) or ρ≥0.8 in a single baseline setting, the improvement in power from a randomized versus non-randomized DD design may be minor. Extensions to cluster study designs and incorporation of time invariant covariates are given. Applications to study planning are illustrated using three real examples with T=4 timepoints and ρ ranging from 0.55 to 0.75.
机译:干预对连续纵向正常结局的干预效果通常是在干预前后进行b≥1干预和k≥1干预后措施的两臂干预研究中估计的,采用“差异分析”(DD)分析。尽管首选随机化,但由于实际限制,通常仍需要非随机设计。对于非随机DD设计,需要结合重复测量相关结构的功效/样本大小估计方法。我们得出干预效果的广义最小二乘(GLS)方差估计。对于通常假定的复合对称(CS)相关结构(其中所有重复测量之间的相关都是常数ρ),这导致可以使用铅笔和纸实现的简单功效和样本大小估计公式。给定总时间点(T)的数量受约束,干预前和干预后的时间点(b = k)尽可能接近相等的数量即可获得最大功效。在计划具有7个或更少时间点的研究时,如果在多个基线量度(b≥2)中具有较大的ρ(ρ≥0.6),在单个基线环境中具有ρ≥0.8,则随机与非随机DD设计的功效会有所提高可能很小。给出了聚类研究设计的扩展和时不变协变量的合并。使用三个真实的示例来说明研究计划的应用,其中T = 4个时间点,ρ在0.55到0.75之间。

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