Raborn Anthony, Savord Andrea, Houts Carrie R, Pease Sheryl, Scippa Kayla, Ramchandren Sindhu
Vector Psychometric Group, LLC, Chapel Hill, NC, USA.
Janssen Research and Development, LLC, Raritan, NJ, USA.
Qual Life Res. 2025 Jun 14. doi: 10.1007/s11136-025-03998-9.
To evaluate the psychometric properties of the Neuro-QoL Fatigue patient-reported outcome measure and its short form when used to assess fatigue in adults living with generalized Myasthenia Gravis (gMG).
Data from Vivacity-MG3 (ClinicalTrials.gov Identifier: NCT04951622), a double-blind placebo-controlled phase 3 study of nipocalimab enrolled 196 participants living with gMG were analyzed. Psychometric analyses of Neuro-QoL Fatigue scores (19-item version and short-form version) focused on data from Baseline and the 24-week double-blind interventional phase of the trial. Factor analytic and classical test theory (CTT) analyses were performed to investigate support for intended Neuro-QoL Fatigue score use, along with convergent and discriminant relationships, known groups analyses, and sensitivity to change analyses. Thresholds to define meaningful within-person change (improvement) over time were also investigated.
The full form factor analytic analyses showed evidence that a unidimensional model adequately fits the data (TLI = 0.99, RMSEA = 0.07), CTT analyses showed high internal consistency (alpha = 0.95), and high test-retest reliability for stable participants (r = 0.92); similar results were observed for the short form. Both versions' scores were correlated with a variety of reference variables at expected levels, demonstrated the ability to differentiate between clinically meaningfully distinct groups, and were significantly correlated with changes in other reference variables. Analyses suggested 19-item and short-form score changes of 6.7 and 7.6, respectively, as showing meaningful improvement over time.
Results provided robust psychometric evidence that supports the use of Neuro-QoL Fatigue scores for assessing fatigue in adults living with gMG.
评估患者报告的神经生活质量疲劳结局指标及其简版在评估全身型重症肌无力(gMG)成年患者疲劳状况时的心理测量特性。
对Vivacity-MG3(ClinicalTrials.gov标识符:NCT04951622)的数据进行分析,该研究是一项关于尼泊卡利单抗的双盲安慰剂对照3期研究,纳入了196例gMG患者。对神经生活质量疲劳评分(19项版本和简版)进行心理测量分析,重点关注试验基线和24周双盲干预阶段的数据。进行因素分析和经典测试理论(CTT)分析,以研究对神经生活质量疲劳评分预期用途的支持情况,以及收敛和区分关系、已知组分析和变化敏感性分析。还研究了定义随时间有意义的个体内变化(改善)的阈值。
完整版本的因素分析表明,有证据显示单维模型能充分拟合数据(TLI = 0.99,RMSEA = 0.07),CTT分析显示内部一致性高(α = 0.95),稳定参与者的重测信度高(r = 0.92);简版也观察到类似结果。两个版本的评分均与各种参考变量在预期水平上相关,证明有能力区分临床意义上明显不同的组,并且与其他参考变量的变化显著相关。分析表明,19项和简版评分分别变化6.7和7.6时,显示随时间有意义的改善。
结果提供了有力的心理测量证据,支持使用神经生活质量疲劳评分来评估gMG成年患者的疲劳状况。