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The Italian version of the Quebec Back Pain Disability Scale: cross-cultural adaptation, reliability and validity in patients with chronic low back pain

机译:意大利版本的魁北克背部疼痛残疾规模:慢性低腰疼痛患者的跨文化适应,可靠性和有效性

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Growing attention is being given to physical functioning measures to assess interventions for low back pain (LBP). The Quebec Back Pain Disability Questionnaire (QBPDS) has never been validated in Italian patients, and the aim of the study was culturally adapting and validating the Italian version of the QBPDS (QBPDS-I), to allow its use with Italian-speaking patients with chronic LBP. The QBPDS-I was developed by means of forward backward translation, a final review by an expert committee and a test of the prefinal version to evaluate its comprehensibility. The psychometric testing included structural validity by exploratory factor analysis (EFA), reliability by internal consistency (Cronbach s alpha) and test retest reliability (intraclass correlation coefficient, ICC 2.1), measurement error by calculating the minimum detectable change (MDC), construct validity by assessing hypotheses of QBPDS correlations with the Roland Morris Disability Scale (RMDQ), the Oswestry Disability Questionnaire (ODI) and a pain numerical rating scale (NRS) (Spearman s correlations). It took one month to develop a consensus-based version of the QBPDS-I. The questionnaire was administered to 201 subjects with chronic LBP and was well accepted. EFA suggested a one-factor 20-item solution (first factor variance explained = 54.7%). Internal consistency ( = 0.95) and test retest reliability (ICC = 0.90) were excellent. The MDC was 12 scale points. Construct validity was good as all of the hypotheses were met; correlations: RMDQ (r = 0.40), ODI (r = 0.48) and NRS (r = 0.44). The QBPDS-I is unidimensional, reliable and valid in patients with chronic LBP. Its use is recommended for clinical and research purposes.
机译:正在延长注意力措施,以评估低腰痛(LBP)的干预措施。魁北克背痛残疾问卷(QBPDS)在意大利患者中从未验证过,该研究的目的是在文化上调整和验证意大利QBPDS(QBPDS-I)的意大利版本,以允许其与意大利语患者一起使用慢性LBP。 QBPDS-I通过前瞻性翻译制定,由专家委员会的最终审查以及PRESTIMP版本的测试来评估其可理解性。心理测量测试包括探索性因子分析(EFA)的结构有效性,内部一致性的可靠性(Cronbach S Alpha)和测试重度可靠性(跨族相关系数,ICC 2.1),通过计算最小可检测变化(MDC),构建有效性来计算测量误差通过评估与罗兰莫里斯残疾秤(RMDQ)的QBPDS相关性的假设,OSWestry残疾问卷(ODI)和止痛数评定量表(NRS)(Spearman S相关)。它花了一个月的时间来制定基于QBPDS-I的基于共识的版本。调查问卷由慢性LBP施用至201个受试者,并受到很好的接受。 EFA建议一个单因素20 - 项目解决方案(第一个因子方差解释= 54.7%)。内部一致性(= 0.95)和测试重度可靠性(ICC = 0.90)优异。 MDC是12个比例点。构建有效性很好,因为所有的假设都满足;相关性:RMDQ(R = 0.40),ODI(r = 0.48)和NRS(r = 0.44)。 QBPDS-I对慢性LBP患者具有单向,可靠,有效,有效。建议使用其使用进行临床和研究目的。

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