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首页> 外文期刊>Italian Journal of Public Health >Determination of Minimum Sample Size Requirement for Multiple Linear Regression and Analysis of Covariance Based on Experimental and Non-experimental Studies
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Determination of Minimum Sample Size Requirement for Multiple Linear Regression and Analysis of Covariance Based on Experimental and Non-experimental Studies

机译:基于实验和非实验研究确定多元线性回归的最小样本量要求和协方差分析

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摘要

Background: MLR and ANCOVA are common statistical techniques and are used for both experimental and non-experimental studies. However, both types of study designs may require different basis of sample size requirement. Therefore, this study aims to proposed sample size guidelines for MLR and ANCOVA for both experimental and non-experimental studies. Methods: We estimated the minimum sample sizes required for MLR and ANCOVA by using Power and Sample Size software (PASS) based on the pre-specified values of alpha, power and effect size (R 2 ). In addition, we also performed validation of the estimates using a real clinical data to evaluate how close the approximations of selected statistics which were derived from the samples were to the actual parameters in the targeted populations. All the coefficients, effect sizes and r-squared obtained from the sample were then compared with their respective parameters in the population. Results: Small minimum sample sizes required for performing both MLR and ANCOVA when r-squared is used as the effect size. However, the validation results based on an evaluation from a real-life dataset suggest that a minimum sample size of 300 or more is necessary to generate a close approximation of estimates with the parameters in the population. Conclusions: We proposed sample size calculation when r-squared is used as an effect size is more suitable for experimental studies. However, taking a larger sample size such as 300 or more is necessary for clinical survey that is conducted in a non-experimental manner.
机译:背景:MLR和ANCOVA是常见的统计技术,用于实验和非实验研究。但是,两种研究设计都可能需要不同的样本量基础。因此,本研究旨在为实验研究和非实验研究提出针对MLR和ANCOVA的样本量指南。方法:我们使用功率和样本量软件(PASS),根据预先指定的alpha,功率和效应量(R 2)值,估算了MLR和ANCOVA所需的最小样本量。此外,我们还使用真实的临床数据对估计值进行了验证,以评估从样本得出的所选统计数据的近似值与目标人群中的实际参数的接近程度。然后将从样本中获得的所有系数,效应大小和r平方与总体中各自的参数进行比较。结果:当使用r平方作为效果量时,执行MLR和ANCOVA所需的最小样本量很小。但是,基于来自现实生活数据集的评估得出的验证结果表明,必须使用最小样本量为300或更大的样本才能生成与总体中的参数近似的估计值。结论:我们建议使用r平方作为有效影响量更适合实验研究时的样本量计算。但是,对于以非实验方式进行的临床调查,需要使用更大的样本量(例如300或更多)。

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