外阴功能状况问卷(VQ)希伯来语版的跨文化适应与验证

Lea Tene, A. Weintraub, Leonid Kalichman
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引用次数: 0

摘要

背景:目前尚无希伯来语外阴功能状态问卷。目的:对希伯来语版本的外阴功能状态问卷(VQ)进行跨文化调整,VQ是一种用于评估女性性交困难的有效工具,并通过检查性交疼痛女性问卷结果与生活质量、焦虑水平和骨盆底功能之间的相关性来评估该版本的心理测量特性。方法:英语版本的VQ根据公认的指南进行了希伯来语的跨文化改编。80名年龄在18岁以上、患有外阴疼痛的希伯来语女性参加了这项研究。参与者完成了vq -希伯来语(VQ-H)(见补充数字内容,可在:http://links.lww.com/JWHPT/A89)、希伯来语版本的健康相关生活质量问卷(SF-12)、盆腔器官脱出/尿失禁性功能问卷(PISQ-12)和状态-特质焦虑量表(STAI)。2 ~ 3周后,所有参与者再次完成VQ-H测试。计算心理测量特性(重测信度、内部一致性、收敛效度和因子分析)。结果:VQ-H具有良好的重测信度,类内相关系数为0.898 ~ 0.958 (P < 0.001);Cronbach α极优(0.935)。VQ-H与SF-12评分之间存在显著相关(r = - 0.360, P = .001)。而VQ-H与STAI、PISQ-12评分的相关性无统计学意义(r = 0.172, P = 0.127, r = - 0.185, P = 0.100)。因子分析揭示了一个4因素的解决方案,代表日常功能和由各种活动引起的或与之相关的疼痛。结论:VQ-H是一种有效可靠的仪器。它的分数反映了在讲希伯来语的女性中外阴疼痛的所有领域的受损功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cross-cultural Adaptation and Validation of the Hebrew Version of the Vulvar Functional Status Questionnaire (VQ)
Background: As yet, no Hebrew language vulvar functional status questionnaire exists. Aims: To perform a cross-cultural adaptation of a Hebrew version of the Vulvar Functional Status Questionnaire (VQ), a validated tool used for evaluating dyspareunia among women, and to evaluate the psychometric properties of this version by examining the correlations between results of the questionnaire among women with pain during intercourse and quality of life, level of anxiety, and pelvic floor function. Methods: The English version of the VQ underwent cross-cultural adaptation to Hebrew according to accepted guidelines. Eighty Hebrew-speaking women with vulvar pain, aged older than 18 years, participated in the study. Participants completed the VQ-Hebrew (VQ-H) (see Supplemental Digital Content, available at: http://links.lww.com/JWHPT/A89), the Hebrew versions of the health-related quality-of-life questionnaire (SF-12), the Pelvic Organ Prolapse/Urinary Incontinence Sexual Function Questionnaire (PISQ-12), and the State-Trait Anxiety Inventory (STAI). All the participants completed the VQ-H again after 2 to 3 weeks. Psychometric properties (test-retest reliability, internal consistency, convergent validity, and factor analysis) were calculated. Results: The VQ-H demonstrated excellent test-retest reliability: intraclass correlation coefficients ranged from 0.898 to 0.958 (P < .001); the Cronbach α was excellent (0.935). A significant correlation was found between the VQ-H and SF-12 scores (r =−0.360, P = .001). However, the correlation between the VQ-H and STAI and PISQ-12 scores was not statistically significant (r = 0.172, P = .127 and r =−0.185, P = .100, respectively). Factor analysis revealed a 4-factor solution representing daily function and pain provoked by or related to various activities. Conclusion: The VQ-H is a valid and reliable instrument. Its scores reflect the impaired function in all domains of vulvar pain among Hebrew-speaking women.
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