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Blinded Sample Size Recalculation in Longitudinal Clinical Trials Using Generalized Estimating Equations

机译:纵向临床试验中使用广义估计方程的盲样本量重新计算

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摘要

In clinical trials in which outcomes are measured repeatedly during the follow-up phase, data analysis is frequently performed using generalized estimating equations (GEEs). Sample size calculation is then especially challenging since in addition to the treatment effect, the intrasubject correlation and the variability of the model error term have to be specified. In this article, the authors investigated by Monte Carlo simulations whether a blinded midcourse estimation of these quantities in an internal pilot study design is feasible in such trials and whether nominal type I and type II error rates are preserved when the estimates are used for sample size recalculation. The actual type I error rates of the blinded sample size recalculation procedure turned out to agree well with the nominal levels. Furthermore, the simulated power was observed to be near the target value as long as the sample size of the internal pilot study was sufficiently high and the bound effects induced by the range of the correlation were limited. The proposed procedure is a helpful tool to achieve robustness of the power with respect to initial misspecifications in the planning stage in clinical trials analyzed by GEE.
机译:在后续阶段中反复测量结果的临床试验中,经常使用广义估计方程(GEE)进行数据分析。然后,样本量的计算尤其具有挑战性,因为除了治疗效果外,还必须指定受试者内部相关性和模型误差项的可变性。在本文中,作者通过蒙特卡洛模拟调查了内部试点研究设计中这些数量的盲中过程估计是否在此类试验中可行,以及在将估计值用于样本量时是否保留了名义I型和II型错误率。重新计算。盲目样本量重新计算程序的实际I类错误率与标称水平很好地吻合。此外,只要内部试点研究的样本量足够高并且相关范围引起的约束效应受到限制,就可以观察到模拟功效接近目标值。拟议的程序是在GEE分析的临床试验的计划阶段中针对初始错误规格实现强大功能的有用工具。

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