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在单项实验设计中改变阶段之前的最佳基线阶段数。

Optimal number of baseline sessions before changing phases within single-case experimental designs.

机构信息

The University of Alabama, Capital Hall 1807, Box 870232, Tuscaloosa, AL, 35487, United States.

The University of Alabama, Capital Hall 1807, Box 870232, Tuscaloosa, AL, 35487, United States.

出版信息

Behav Processes. 2021 Oct;191:104461. doi: 10.1016/j.beproc.2021.104461. Epub 2021 Jul 16.

Abstract

Recommendations vary considerably for the minimum or optimal number of baseline sessions to conduct within single-case experimental design clinical analyses or research studies. We examined the optimal number of baseline sessions that produced minimal bias. First, we examined the relation between the number of baseline sessions and the degree of bias in calculating estimates of treatment effect size. As the number of baseline sessions increased, the bias in effect size estimates decreased, r = -0.36, p < 0.001. s, we examined what would be the minimum number of baseline sessions associated with varying levels of bias. Bias of approximately ten percent was associated with four to five baseline sessions. Bias of about five percent was associated with six to seven baseline sessions. Third, we examined the relation between standard deviation and varying levels of bias. As the number of baseline sessions increases, the standard deviation for the phase decreased, r = -0.89, p < 0.001. Fourth, we examined what value of standard deviation in the baseline phase was associated with equal to or more than five versus ten percent bias. When considering five or ten percent bias, the optimal level of standard deviation was 0.59 or less.

摘要

建议在单案例实验设计临床分析或研究中进行的基线阶段的最小或最佳次数变化很大。我们研究了产生最小偏差的最佳基线阶段次数。首先,我们研究了基线阶段次数与治疗效果大小估计偏差程度之间的关系。随着基线阶段次数的增加,效果大小估计的偏差减小,r = -0.36,p < 0.001。其次,我们研究了与不同程度偏差相关的最小基线阶段次数。大约百分之十的偏差与四到五个基线阶段相关。大约百分之五的偏差与六到七个基线阶段相关。第三,我们研究了标准差与不同程度偏差之间的关系。随着基线阶段次数的增加,阶段的标准差降低,r = -0.89,p < 0.001。第四,我们研究了基线阶段的标准差值与等于或大于 5%或 10%的偏差之间的关系。当考虑 5%或 10%的偏差时,最佳标准差水平为 0.59 或更低。

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