Content Validity and Psychometric Evaluation of the Crohn’s Symptom Severity (CSS) Questionnaire in Patients with Moderately to Severely Active Crohn’s Disease

IF 3.4 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Advances in Therapy Pub Date : 2024-08-06 DOI:10.1007/s12325-024-02923-9
Edouard Louis, Wan-Ju Lee, Leighann Litcher-Kelly, Sarah Ollis, Emma Pranschke, Kristina Fitzgerald, Ana Paula Lacerda, Ezequiel Neimark, Yuri Sanchez Gonzalez, Julian Panés
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Abstract

Introduction

Individuals living with Crohn’s disease (CD) experience burdensome symptoms. As such, it is important to measure CD symptom severity in clinical research. The goal of this study was to evaluate the content validity, psychometric performance, and score interpretability of a new patient-reported instrument, the Crohn’s Symptom Severity (CSS) questionnaire, among adolescents and adults with moderately to severely active CD.

Methods

Cognitive debriefing interviews (N = 30; n = 20 adults, n = 10 adolescents) were conducted to evaluate the content validity of the CSS. Additionally, the CSS scores were evaluated for reliability and validity using data from a phase 3 randomized clinical trial of risankizumab (NCT03105128; N = 850). Meaningful within-patient change (MWPC) thresholds were estimated using anchor-based methods.

Results

All interview participants (n = 30/30, 100.00%) reported the CSS was easy to complete and most participants (n = 28/29, 96.55%) reported that the CSS was relevant to their experience of CD. Among the clinical trial subjects (N = 850) the following was found for the CSS: mostly acceptable item–total correlations (0.26–0.79); weak to moderate inter-item correlations (r = 0.07–0.57), good internal consistency (Cronbach’s α = 0.76–0.87); intraclass correlation coefficients ranged from 0.48 to 0.70, not consistently exceeding the acceptable range for test–retest reliability (0.70); acceptable convergent validity and known-groups results; and demonstrated sensitivity to change. Analyses supported an MWPC estimate of 6–11 points.

Conclusions

This study supports use of the CSS for measuring CD symptoms and sleep impact among adolescents and adults aged 16 and older with moderately to severely active CD in clinical research.

Trial Registration

NCT03105128 (registration date 4 April 2017).

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中度至重度活动性克罗恩病患者克罗恩症状严重程度 (CSS) 问卷的内容有效性和心理测量学评估。
导言:克罗恩病(CD)患者的症状令人不堪重负。因此,在临床研究中测量克罗恩病症状的严重程度非常重要。本研究的目的是评估新的患者报告工具--克罗恩病症状严重程度(CSS)问卷--在患有中度至重度活动性克罗恩病的青少年和成人中的内容有效性、心理测量性能和分数可解释性:方法:进行认知汇报访谈(N = 30;n = 20 名成人,n = 10 名青少年),以评估 CSS 的内容效度。此外,还利用利抗珠单抗 3 期随机临床试验(NCT03105128;N = 850)的数据对 CSS 评分的可靠性和有效性进行了评估。采用基于锚的方法估算了患者内部有意义变化(MWPC)阈值:所有受试者(n = 30/30,100.00%)都表示 CSS 很容易完成,大多数受试者(n = 28/29,96.55%)表示 CSS 与他们的 CD 经历相关。在临床试验受试者(N = 850)中,我们发现 CSS 具有以下特点:大部分项目-总相关性(0.26-0.79)可以接受;项目间相关性弱到中等(r = 0.07-0.57);良好的内部一致性(Cronbach's α = 0.76-0.87);类内相关系数从 0.48 到 0.70 不等,没有持续超过测试-再测可靠性的可接受范围(0.70);收敛效度和已知组结果均可接受;对变化表现出敏感性。分析结果表明,MWPC 的估计值为 6-11 分:本研究支持在临床研究中使用CSS测量16岁及以上患有中度至重度活动性CD的青少年和成人的CD症状和睡眠影响:NCT03105128(注册日期:2017年4月4日)。
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来源期刊
Advances in Therapy
Advances in Therapy 医学-药学
CiteScore
7.20
自引率
2.60%
发文量
353
审稿时长
6-12 weeks
期刊介绍: Advances in Therapy is an international, peer reviewed, rapid-publication (peer review in 2 weeks, published 3–4 weeks from acceptance) journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of therapeutics and interventions (including devices) across all therapeutic areas. Studies relating to diagnostics and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. The journal is of interest to a broad audience of healthcare professionals and publishes original research, reviews, communications and letters. The journal is read by a global audience and receives submissions from all over the world. Advances in Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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