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在一个具有代表性的德国样本中对简明症状量表18(BSI-18)进行心理测量分析。

Psychometric analysis of the brief symptom inventory 18 (BSI-18) in a representative German sample.

作者信息

Franke Gabriele Helga, Jaeger Susanne, Glaesmer Heide, Barkmann Claus, Petrowski Katja, Braehler Elmar

机构信息

Department of Rehabilitation Psychology, University of Applied Sciences Magdeburg-Stendal, Osterburger Str. 25, 39576, Hansestadt Stendal, Germany.

Department of Medical Psychology and Medical Sociology, University of Leipzig, Leipzig, Germany.

出版信息

BMC Med Res Methodol. 2017 Jan 26;17(1):14. doi: 10.1186/s12874-016-0283-3.

Abstract

BACKGROUND

The BSI-18 contains the three six-item scales somatization, depression, and anxiety as well as the Global Severity Index (GSI), including all 18 items. The BSI-18 is the latest and shortest of the multidimensional versions of the Symptom-Checklist 90-R, but its psychometric properties have not been sufficiently clarified yet.

METHODS

Based on a representative sample of N = 2516 participants (aged 14-94 years), detailed psychometric analyses were carried out.

RESULTS

The internal consistency was good: Somatization α = .82, Depression α = .87, Anxiety α = .84 and GSI α = .93. Confirmatory factor analysis supported the three scales as second-order and GSI as first-order factors. The model fit based on RMSEA is good but that model fit based on CFI and TLI are too low.

CONCLUSIONS

Therefore, it is a very short, reliable instrument for the assessment of psychological distress. The BSI-18 can be used to reliably assess psychological distress in the general population. However, further studies need to evaluate the usefulness of standardization in clinical samples.

摘要

背景

BSI - 18包含三个六项量表,即躯体化、抑郁和焦虑量表以及包含所有18个条目的总体严重程度指数(GSI)。BSI - 18是症状自评量表90 - R多维度版本中最新且最短的版本,但其心理测量特性尚未得到充分阐明。

方法

基于N = 2516名参与者(年龄14 - 94岁)的代表性样本进行了详细的心理测量分析。

结果

内部一致性良好:躯体化α = 0.82,抑郁α = 0.87,焦虑α = 0.84,总体严重程度指数α = 0.93。验证性因素分析支持这三个量表为二阶因素,总体严重程度指数为一阶因素。基于RMSEA的模型拟合良好,但基于CFI和TLI的模型拟合度较低。

结论

因此,它是一种用于评估心理困扰的非常简短且可靠的工具。BSI - 18可用于可靠地评估普通人群的心理困扰。然而,需要进一步研究评估其在临床样本中标准化的有用性。

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