首页> 外文OA文献 >\u3cem\u3ePowerUp!\u3c/em\u3e: A Tool for Calculating Minimum Detectable Effect Sizes and Minimum Required Sample Sizes for Experimental and Quasi-Experimental Design Studies
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\u3cem\u3ePowerUp!\u3c/em\u3e: A Tool for Calculating Minimum Detectable Effect Sizes and Minimum Required Sample Sizes for Experimental and Quasi-Experimental Design Studies

机译:\ u3cem \ u3ePowerUp!\ u3c / em \ u3e:一种用于计算实验和拟实验设计研究的最小可检测效应量和所需最小样本量的工具

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摘要

This paper complements existing power analysis tools by offering tools to compute minimum detectable effect sizes (MDES) for existing studies and to estimate minimum required sample sizes (MRSS) for studies under design. The tools that accompany this paper support estimates of MDES or MSSR for 21 different study designs that include 14 random assignment designs (6 designs in which individuals are randomly assigned to treatment or control condition and 8 in which clusters of individuals are randomly assigned to condition, with models differing depending on whether the sample was blocked prior to random assignment and by whether the analytic models assume constant, fixed, or random effects across blocks or assignment clusters); and 7 quasi-experimental designs (an interrupted time series design and 6 regression discontinuity designs that vary depending on whether the sample was blocked prior to randomization, whether individuals or clusters of individuals are assigned to treatment or control condition, and whether the analytic models assume fixed or random effects).
机译:本文通过提供工具来计算现有研究的最小可检测效应量(MDES)并估算正在设计中的研究的最小所需样本量(MRSS),从而对现有的功率分析工具进行补充。本文附带的工具支持21种不同研究设计的MDES或MSSR估算,其中包括14种随机分配设计(其中6种设计将患者随机分配给治疗或控制条件,而8种设计将个体集群随机分配给条件或控制条件,模型的不同取决于样本是否在随机分配之前被阻塞,以及分析模型在整个块或分配群中是否具有恒定,固定或随机的影响);和7种准实验设计(中断时间序列设计和6种回归间断设计),这些设计根据样本在随机化之前是否被封闭,是否将个体或个体群分配给治疗或对照条件以及是否采用分析模型而有所不同固定或随机效果)。

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