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更详细地探讨 t 检验的基本假设:正态性和样本量。

More about the basic assumptions of t-test: normality and sample size.

机构信息

Department of Anesthesia and Pain Medicine, Pusan National University School of Medicine, Busan, Korea.

Department of Anesthesiology and Pain Medicine, Haeundae Paik Hospital, Inje University College of Medicine, Busan, Korea.

出版信息

Korean J Anesthesiol. 2019 Aug;72(4):331-335. doi: 10.4097/kja.d.18.00292. Epub 2019 Apr 1.

Abstract

Most parametric tests start with the basic assumption on the distribution of populations. The conditions required to conduct the t-test include the measured values in ratio scale or interval scale, simple random extraction, normal distribution of data, appropriate sample size, and homogeneity of variance. The normality test is a kind of hypothesis test which has Type I and II errors, similar to the other hypothesis tests. It means that the sample size must influence the power of the normality test and its reliability. It is hard to find an established sample size for satisfying the power of the normality test. In the current article, the relationships between normality, power, and sample size were discussed. As the sample size decreased in the normality test, sufficient power was not guaranteed even with the same significance level. In the independent t-test, the change in power according to sample size and sample size ratio between groups was observed. When the sample size of one group was fixed and that of another group increased, power increased to some extent. However, it was not more efficient than increasing the sample sizes of both groups equally. To ensure the power in the normality test, sufficient sample size is required. The power is maximized when the sample size ratio between two groups is 1 : 1.

摘要

大多数参数检验都基于对总体分布的基本假设。进行 t 检验需要满足以下条件:度量值为等比或等距尺度、简单随机抽样、数据正态分布、适当的样本量和方差同质性。正态性检验是一种假设检验,与其他假设检验一样存在 I 型和 II 型错误。这意味着样本量必须影响正态性检验的功效及其可靠性。很难找到满足正态性检验功效的既定样本量。本文讨论了正态性、功效和样本量之间的关系。随着正态性检验中的样本量减少,即使在相同的显著性水平下,也不能保证有足够的功效。在独立 t 检验中,观察了根据样本量和组间样本量比变化的功效。当一组的样本量固定而另一组的样本量增加时,功效会在一定程度上增加。但它并不比等比例增加两组的样本量更有效。为了确保正态性检验的功效,需要足够的样本量。当两组的样本量比为 1:1 时,功效达到最大值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b9/6676026/193cc86da992/kja-d-18-00292f1.jpg

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