Patient-Reported Outcomes in Huntington's Disease: Quality of Life in Neurological Disorders (Neuro-QoL) and Huntington's Disease Health-Related Quality of Life (HDQLIFE) Physical Function Measures

被引:12
|
作者
Carlozzi, Noelle E. [1 ]
Ready, Rebecca E. [2 ]
Frank, Samuel [3 ]
Cella, David [4 ,5 ]
Hahn, Elizabeth A. [5 ]
Goodnight, Siera M. [1 ]
Schilling, Stephen G. [1 ,6 ]
Boileau, Nicholas R. [1 ]
Dayalu, Praveen [7 ]
机构
[1] Univ Michigan, Dept Phys Med & Rehabil, North Campus Res Complex,2800 Plymouth Rd, Ann Arbor, MI 48109 USA
[2] Univ Massachusetts, Dept Psychol & Brain Sci, Amherst, MA 01003 USA
[3] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[4] Northwestern Univ, Inst Hlth Serv Res & Policy Studies, Feinberg Sch Med, Chicago, IL 60611 USA
[5] Northwestern Univ, Dept Med Social Sci, Chicago, IL 60611 USA
[6] Univ Michigan, Inst Social Res, Ann Arbor, MI USA
[7] Univ Michigan, Dept Neurol, Ann Arbor, MI USA
基金
美国国家卫生研究院;
关键词
Neuro-QoL; HDQLIFE; Huntington's disease; physical functioning; chorea; motor symptoms; health-related quality of life; patient-reported outcome (PRO); CONTROLLED-TRIAL; EXERCISE PROGRAM; CLINICAL-TRIALS; PROGRESSION; PEOPLE; CHOREA; HD; FEASIBILITY; PREMANIFEST; DIAGNOSIS;
D O I
10.1002/mds.27046
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: There is a need for patient-reported outcome measures that capture the impact that motor impairments have on health-related quality of life in individuals with Huntington's disease. Objectives: The objectives of this study were to establish the reliability and validity of new physical functioning patient-reported outcome measures in Huntington's disease. Methods: A total of 510 individuals with Huntington's disease completed 2 Quality of Life in Neurological Disorders (Lower Extremity Function and Upper Extremity Function) and 3 Huntington's Disease Health-Related Quality of Life (Chorea, Speech Difficulties, and Swallowing Difficulties) measures. Clinician-rated and generic self-report measures were also administered. Results: Reliabilities for the new patient reported physical functioning measures were excellent (all Cronbach's a >.92). Convergent, discriminant validity and known group validity was supported. Conclusions: The results provide psychometric support for new patient-reported physical functioning measures and the fact that these measures can be used as clinically meaningful endpoints in Huntington's disease research and clinical practice. (C) 2017 International Parkinson and Movement Disorder Society
引用
收藏
页码:1096 / 1102
页数:8
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