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Sample size needed for maximum likelihood factor analysis, principal component analysis, and principal factor analysis.

机译:最大似然因子分析,主成分分析和主因子分析所需的样本大小。

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摘要

This study investigated the applicability of Ke's (2001) findings regarding the relationships among the sample size, the number of variables, the number of factors, and the level of communality in exploratory factor analysis to a live dataset. A second purpose was to extend Ke's findings, obtained only for maximum likelihood analysis (MLFA), to principal factor analysis (PFA) and principal component analysis (PCA). To accomplish these purposes, live data from a large dataset consisting of 9468 observations from the Millon Clinical Multiaxial Inventory-III (MCMI-III) were factor analyzed using MLFA, PCA, and PFA. Three methods were employed to determine the number of factors to be extracted. Additionally, a variety of factor conditions were generated from the live data to create subpopulation conditions with varying numbers of factors and variable to factor ratios. Random samples were repeatedly drawn from the population and subpopulation conditions. Coefficients of congruence between the population/subpopulation and sample solutions were determined for three values of congruence (0.92, 0.95, and 0.98). The results were then compared with Ke's (2001) guidelines for the minimum sample size needed for factor analysis. Three major findings emerged. First, when the factor structure was well defined, Ke's (2001) guidelines were conservative. Second, when the factor structure was poorly defined, the minimum required sample sizes observed were close to, but inconsistent with, Ke's guidelines. Third, the minimum sample sizes needed to obtain good, very good, and excellent congruence were comparable among MLFA, PCA, and PFA. Additionally, the minimum sample size was influenced by the number of factors retained, the similarity in the number of variables loading on each factor, the number of variables sharing loadings on more than one factor, and underfactoring and overfactoring the data. Based on factor analysis of one live dataset and subpopulations from that dataset, Ke's guidelines may provide a conservative estimate for the minimum sample sizes needed for good and excellent congruence.
机译:这项研究调查了Ke(2001)关于样本大小,变量数量,因子数量以及探索性因子分析中的社区水平之间的关系的实时数据集的适用性。第二个目的是将仅针对最大似然分析(MLFA)获得的Ke的发现扩展到主因子分析(PFA)和主成分分析(PCA)。为了实现这些目的,使用MLFA,PCA和PFA对来自Millon临床多轴清单III(MCMI-III)的9468个观测值组成的大型数据集的实时数据进行了因子分析。采用三种方法确定要提取的因子数量。另外,从实时数据中生成了多种因子条件,以创建具有不同数量因子和可变因子比例的亚种群条件。从人口和亚人群条件中反复抽取随机样本。对于三个一致性值(0.92、0.95和0.98),确定了总体/亚群与样品溶液之间的一致性系数。然后将结果与Ke's(2001)的指南进行比较,得出因子分析所需的最小样本量。出现了三个主要发现。首先,当因素结构得到很好的定义时,Ke(2001)的指南是保守的。第二,当因子结构定义不明确时,观察到的最小所需样本量接近但与Ke的准则不符。第三,在MLFA,PCA和PFA中,获得良好,非常好的和优异的一致性所需的最小样本量是可比的。此外,最小样本量受到以下因素的影响:保留的因子数量,每个因子上加载的变量数量的相似性,共享一个以上因子上的加载变量的数量以及对数据的分解不足和分解过度。基于对一个活数据集和该数据集中的子种群的因子分析,Ke的准则可能会保守地估计良好和优异一致性所需的最小样本量。

著录项

  • 作者

    McFann, Kimberly K.;

  • 作者单位

    University of Northern Colorado.;

  • 授予单位 University of Northern Colorado.;
  • 学科 Statistics.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 206 p.
  • 总页数 206
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:46:43

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