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问卷预测试的样本量。

Sample size for pre-tests of questionnaires.

作者信息

Perneger Thomas V, Courvoisier Delphine S, Hudelson Patricia M, Gayet-Ageron Angèle

机构信息

Division of Clinical Epidemiology, University Hospitals of Geneva, 6 rue Gabrielle-Perret-Gentil, 1211, Geneva, Switzerland,

出版信息

Qual Life Res. 2015 Jan;24(1):147-51. doi: 10.1007/s11136-014-0752-2. Epub 2014 Jul 10.

Abstract

PURPOSE

To provide guidance regarding the desirable size of pre-tests of psychometric questionnaires, when the purpose of the pre-test is to detect misunderstandings, ambiguities, or other difficulties participants may encounter with instrument items (called «problems»).

METHODS

We computed (a) the power to detect a problem for various levels of prevalence and various sample sizes, (b) the required sample size to detect problems for various levels of prevalence, and (c) upper confidence limits for problem prevalence in situations where no problems were detected.

RESULTS

As expected, power increased with problem prevalence and with sample size. If problem prevalence was 0.05, a sample of 10 participants had only a power of 40 % to detect the problem, and a sample of 20 achieved a power of 64 %. To achieve a power of 80 %, 32 participants were necessary if the prevalence of the problem was 0.05, 16 participants if prevalence was 0.10, and 8 if prevalence was 0.20. If no problems were observed in a given sample, the upper limit of a two-sided 90 % confidence interval reached 0.26 for a sample size of 10, 0.14 for a sample size of 20, and 0.10 for a sample of 30 participants.

CONCLUSIONS

Small samples (5-15 participants) that are common in pre-tests of questionaires may fail to uncover even common problems. A default sample size of 30 participants is recommended.

摘要

目的

当预测试的目的是检测参与者在心理测量问卷项目中可能遇到的误解、歧义或其他困难(称为“问题”)时,提供关于预测试理想规模的指导。

方法

我们计算了(a)在不同患病率水平和不同样本量下检测问题的功效,(b)在不同患病率水平下检测问题所需的样本量,以及(c)在未检测到问题的情况下问题患病率的上置信限。

结果

正如预期的那样,功效随着问题患病率和样本量的增加而提高。如果问题患病率为0.05,10名参与者的样本检测到问题的功效仅为40%,20名参与者的样本功效为64%。要达到80%的功效,如果问题患病率为0.05,则需要32名参与者;如果患病率为0.10,则需要16名参与者;如果患病率为0.20,则需要8名参与者。如果在给定样本中未观察到问题,对于样本量为10的情况,双侧90%置信区间的上限达到0.26;对于样本量为20的情况,上限为0.

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