Sample size determination for quadratic inference functions in longitudinal design with dichotomous outcomes

被引:6
|
作者
Hu, Youna [1 ]
Song, Peter X. -K. [1 ]
机构
[1] Univ Michigan, Dept Biostat, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
average risk; clinical trial; correlation structure; GEE; marginal model; power;
D O I
10.1002/sim.4458
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Quadratic inference functions (QIF) methodology is an important alternative to the generalized estimating equations (GEE) method in the longitudinal marginal model, as it offers higher estimation efficiency than the GEE when correlation structure is misspecified. The focus of this paper is on sample size determination and power calculation for QIF based on the Wald test in a marginal logistic model with covariates of treatment, time, and treatmenttime interaction. We have made three contributions in this paper: (i) we derived formulas of sample size and power for QIF and compared their performance with those given by the GEE; (ii) we proposed an optimal scheme of sample size determination to overcome the difficulty of unknown true correlation matrix in the sense of minimal average risk; and (iii) we studied properties of both QIF and GEE sample size formulas in relation to the number of follow-up visits and found that the QIF gave more robust sample sizes than the GEE. Using numerical examples, we illustrated that without sacrificing statistical power, the QIF design leads to sample size saving and hence lower study cost in comparison with the GEE analysis. We conclude that the QIF analysis is appealing for longitudinal studies. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:787 / 800
页数:14
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