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Sample size determination for testing equality in frequency data under an incomplete block crossover design

机译:不完全块交叉设计下用于测试频率数据相等性的样本大小确定

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When there are more than two treatments under comparison, we may consider the use of the incomplete block crossover design (IBCD) to save the number of patients needed for a parallel groups design and reduce the duration of a crossover trial. We develop an asymptotic procedure for simultaneously testing equality of two treatments versus a control treatment (or placebo) in frequency data under the IBCD with two periods. We derive a sample size calculation procedure for the desired power of detecting the given treatment effects at a nominal-level and suggest a simple ad hoc adjustment procedure to improve the accuracy of the sample size determination when the resulting minimum required number of patients is not large. We employ Monte Carlo simulation to evaluate the finite-sample performance of the proposed test, the accuracy of the sample size calculation procedure, and that with the simple ad hoc adjustment suggested here. We use the data taken as a part of a crossover trial comparing the number of exacerbations between using salbutamol or salmeterol and a placebo in asthma patients to illustrate the sample size calculation procedure.
机译:当比较两种以上的治疗方法时,我们可以考虑使用不完全阻滞交叉设计(IBCD),以节省平行组设计所需的患者数量,并减少交叉试验的持续时间。我们开发了一种渐进程序,用于在IBCD下的两个周期的频率数据中同时测试两种治疗与对照治疗(或安慰剂)的相等性。我们导出了样本量计算程序,用于以名义水平检测给定治疗效果的所需功率,并建议了一种简单的临时调整程序,以在最终所需的最小患者人数不多时提高样本量确定的准确性。我们采用蒙特卡洛模拟来评估所提出测试的有限样本性能,样本大小计算过程的准确性以及此处建议的简单临时调整的准确性。我们使用作为交叉试验一部分的数据,比较哮喘患者中沙丁胺醇或沙美特罗与安慰剂之间加重的次数,以说明样本量计算程序。

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