Wild D, Patrick D, Johnson E, Berzon R, Wald A
Metris Research, Embankment, London, UK.
Qual Life Res. 1995 Dec;4(6):532-9. doi: 10.1007/BF00634748.
A disease-specific measure was needed for use in an international clinical trial to evaluate an investigational drug for genital herpes. A new measure was developed initially in the UK and translated and adapted for use in France, Italy, Germany, Denmark, Spain and the USA. This paper describes the translation and adaptation of the USA measure. It also describes the assessment of internal consistency, reproducibility, content validity, and construct validity (convergent and discriminant) of the measure. Two outcome measures of the final genital herpes-specific measure were developed: (1) a 21-item symptoms subscale; and (2) a 20-item HRQOL subscale. Each measure was scored and analyzed separately; the psychometric testing discussed in this paper refers to the HRQOL subscale only. The internal consistency of the HRQOL subscale is high (r = 0.93), as is the reproducibility measured with a two week interval (r = 0.85). Convergent validity is moderate to high. (Fleming Self-Regard subscale, r = 0.48; SF-36 Social Functioning dimension r = 0.59; SF-36 Mental Health dimension r = 0.50). The number of herpes outbreaks in the past year was a significant predictor of scores on the HRQOL subscale (0-1 outbreaks, mean = 82.1; 2+ outbreaks, mean = 72.1, p = 0.058) suggesting discriminant validity. The measure is currently in a phase III clinical trial including anti-viral therapy where the question of responsiveness can be addressed.
在一项国际临床试验中,需要一种针对特定疾病的测量方法来评估一种用于治疗生殖器疱疹的研究性药物。一种新的测量方法最初在英国开发,然后被翻译并改编用于法国、意大利、德国、丹麦、西班牙和美国。本文描述了美国测量方法的翻译和改编过程。它还描述了该测量方法的内部一致性、可重复性、内容效度和结构效度(收敛效度和区分效度)的评估。最终的生殖器疱疹特异性测量方法产生了两个结果测量指标:(1)一个包含21个条目的症状子量表;(2)一个包含20个条目的健康相关生活质量子量表。每个测量指标分别进行评分和分析;本文讨论的心理测量测试仅指健康相关生活质量子量表。健康相关生活质量子量表的内部一致性较高(r = 0.93),两周间隔测量的可重复性也较高(r = 0.85)。收敛效度为中度到高度。(弗莱明自尊子量表,r = 0.48;SF-36社会功能维度,r = 0.59;SF-36心理健康维度,r = 0.50)。过去一年中疱疹发作的次数是健康相关生活质量子量表得分的一个显著预测因素(0 - 1次发作,平均值 = 82.1;2次及以上发作,平均值 = 72.1,p = 0.058),表明具有区分效度。该测量方法目前正处于一项包括抗病毒治疗的III期临床试验中,在该试验中可以解决反应性的问题。