Li Dateng, Zhang Song, Cao Jing
Department of Statistical Science, Southern Methodist University, Dallas, Texas.
Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, Texas.
Stat Med. 2019 Dec 10;38(28):5413-5427. doi: 10.1002/sim.8378. Epub 2019 Oct 25.
Statistical inference based on correlated count measurements are frequently performed in biomedical studies. Most of existing sample size calculation methods for count outcomes are developed under the Poisson model. Deviation from the Poisson assumption (equality of mean and variance) has been widely documented in practice, which indicates urgent needs of sample size methods with more realistic assumptions to ensure valid experimental design. In this study, we investigate sample size calculation for clinical trials with correlated count measurements based on the negative binomial distribution. This approach is flexible to accommodate overdispersion and unequal measurement intervals, as well as arbitrary randomization ratios, missing data patterns, and correlation structures. Importantly, the derived sample size formulas have closed forms both for the comparison of slopes and for the comparison of time-averaged responses, which greatly reduces the burden of implementation in practice. We conducted extensive simulation to demonstrate that the proposed method maintains the nominal levels of power and type I error over a wide range of design configurations. We illustrate the application of this approach using a real epileptic trial.
基于相关计数测量的统计推断在生物医学研究中经常进行。现有的大多数计数结果样本量计算方法都是在泊松模型下开发的。在实际中,与泊松假设(均值和方差相等)的偏差已被广泛记录,这表明迫切需要具有更现实假设的样本量方法,以确保有效的实验设计。在本研究中,我们研究基于负二项分布的具有相关计数测量的临床试验的样本量计算。这种方法灵活,能够适应过度离散和不等的测量间隔,以及任意随机化比例、缺失数据模式和相关结构。重要的是,推导的样本量公式对于斜率比较和时间平均反应比较都有封闭形式,这大大减轻了实际实施的负担。我们进行了广泛的模拟,以证明所提出的方法在广泛的设计配置中保持了名义检验效能水平和I型错误。我们使用一个真实的癫痫试验来说明这种方法的应用。