Turner Rebecca M, Prevost A Toby, Thompson Simon G
MRC Biostatistics Unit, Institute of Public Health, Robinson Way, Cambridge CB2 2SR, U.K.
Stat Med. 2004 Apr 30;23(8):1195-214. doi: 10.1002/sim.1721.
The sample size required for a cluster randomized trial depends on the magnitude of the intracluster correlation coefficient (ICC). The usual sample size calculation makes no allowance for the fact that the ICC is not known precisely in advance. We develop methods which allow for the uncertainty in a previously observed ICC, using a variety of distributional assumptions. Distributions for the power are derived, reflecting this uncertainty. Further, the observed ICC in a future study will not equal its true value, and we consider the impact of this on power. We implement calculations within a Bayesian simulation approach, and provide one simplification that can be performed using simple simulation within spreadsheet software. In our examples, recognizing the uncertainty in a previous ICC estimate decreases expected power, especially when the power calculated naively from the ICC estimate is high. To protect against the possibility of low power, sample sizes may need to be very substantially increased. Recognizing the variability in the future observed ICC has little effect if prior uncertainty has already been taken into account. We show how our method can be extended to the case in which multiple prior ICC estimates are available. The methods presented in this paper can be used by applied researchers to protect against loss of power, or to choose a design which reduces the impact of uncertainty in the ICC.
整群随机试验所需的样本量取决于整群内相关系数(ICC)的大小。通常的样本量计算没有考虑到ICC事先并不能精确得知这一事实。我们开发了一些方法,利用各种分布假设来考虑先前观察到的ICC中的不确定性。推导了反映这种不确定性的检验效能分布。此外,未来研究中观察到的ICC将不等于其真实值,我们考虑了这对检验效能的影响。我们在贝叶斯模拟方法中进行计算,并提供一种可以在电子表格软件中使用简单模拟执行的简化方法。在我们的示例中,认识到先前ICC估计中的不确定性会降低预期检验效能,尤其是当根据ICC估计天真地计算出的检验效能较高时。为了防止检验效能较低的可能性,样本量可能需要大幅增加。如果已经考虑了先前的不确定性,那么认识到未来观察到的ICC的变异性影响很小。我们展示了如何将我们的方法扩展到有多个先前ICC估计值可用的情况。本文提出的方法可供应用研究人员使用,以防止检验效能损失,或选择一种减少ICC不确定性影响的设计。