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Cross-Cultural Adaptation and Validation of the Italian Version of the Voice Symptom Scale (I-VoiSS)

机译:跨文化适应与验证意大利文字语音症状规模(I-Voiss)

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Summary Objectives To evaluate the reliability and validity of the Italian Voice Symptom Scale (I-VoiSS). Study Design Cross-sectional, nonrandomized, prospective study with controls. Methods The study consisted of five phases: item generation, reliability analysis, normative data generation, validity and responsiveness analysis. A group of 113 dysphonic patients was enrolled for the internal consistency analysis. Seventy-three of them completed the I-VoiSS twice, 2 weeks apart, for test-retest reliability analysis. A group of 150 vocally healthy participants completed the I-VoiSS for normative data generation. I-VoiSS scores obtained by dysphonic and vocally healthy participants were compared for validity analysis. I-VoiSS scores were correlated with those of the Italian version of the Voice Handicap Index (I-VHI) in 49 dysphonic patients for criterion validity analysis. I-VoiSS scores obtained in a group of 37 nonsmoker dysphonic patients before and after surgical treatment for vocal fold polyps were compared for responsiveness analysis. Finally, the cutoff value of the I-VoiSS was calculated. Results All the enrolled participants managed to complete the I-VoiSS autonomously. Internal consistency and test-retest were satisfactory (?= 0.92 and r = 0.91). A significant difference in the I-VoiSS scores between the dysphonic and vocally healthy participants was found ( p = 0.001). Positive significant correlations were found between I-VoiSS and I-VHI scores ( r = 0.85). I-VoiSS scores obtained in the pretreatment condition were significantly higher than those obtained after surgery ( p = 0.001). The cutoff value of I-VoiSS was 15.5. Conclusion I-VoiSS is reliable, valid, responsive to changes, and recommended for clinical practice and outcome research.
机译:摘要目的,评估意大利语音症状规模的可靠性和有效性(I-Voiss)。研究设计横断面,非扫描,前瞻性研究。方法该研究由五个阶段:项目生成,可靠性分析,规范数据生成,有效性和响应性分析组成。注册了113名困扰患者的内部一致性分析。其中七十三个完成了两次,分别2周,用于测试 - 保持最可靠性分析。一组150名声道,社会健康参与者完成了I-Voiss for规范数据生成。使用困难和声乐健康的参与者获得的I-Voiss分数用于有效分析。 I-Voiss分数与49名困难患者的语音障碍指数(I-VHI)的意大利版本的分数相关,以获得标准有效性分析。比较了在37名非主持人困扰患者中获得的I-Voiss分数,以前和后期后的声带息肉息肉进行了响应性分析。最后,计算了I-Voiss的截止值。结果所有注册的参与者都设法自主地完成I-VOISS。内部一致性和测试重新测试是令人满意的(?= 0.92和r = 0.91)。发现了困难和声带与声学健康参与者之间的I-Voiss评分的显着差异(p = 0.001)。在I-Voiss和I-VHI分数之间发现了正显着相关性(r = 0.85)。在预处理条件下获得的I-Voiss分数明显高于手术后获得的分数(P = 0.001)。 I-Voiss的截止值为15.5。结论I-Voiss是可靠的,有效的,响应于变化,并推荐用于临床实践和结果研究。

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