Constraint-Induced Movement Therapy for the Lower Extremities in Multiple Sclerosis: Case Series With 4-Year Follow-Up

被引:25
作者
Mark, Victor W. [1 ,2 ,3 ]
Taub, Edward [3 ]
Uswatte, Gitendra [3 ,4 ]
Bashir, Khurram [2 ]
Cutter, Gary R. [5 ]
Bryson, Camille C. [3 ]
Bishop-McKay, Staci [3 ]
Bowman, Mary H. [3 ]
机构
[1] Univ Alabama Birmingham, Dept Phys Med & Rehabil, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Neurol, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Dept Psychol, Birmingham, AL 35294 USA
[4] Univ Alabama Birmingham, Dept Phys Therapy, Birmingham, AL 35294 USA
[5] Univ Alabama Birmingham, Dept Biostat, Birmingham, AL 35294 USA
来源
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION | 2013年 / 94卷 / 04期
基金
美国国家卫生研究院;
关键词
Mobility limitation; Multiple sclerosis; Physical therapy specialty; Recovery of function; Rehabilitation; PHYSICAL-ACTIVITY; COMBINED EXERCISE; LEARNED NONUSE; STROKE; REHABILITATION; DISABILITY; INTERVENTION; MOBILITY; OUTCOMES; APHASIA;
D O I
10.1016/j.apmr.2012.09.032
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Objective: To evaluate in a preliminary manner the feasibility, safety, and efficacy of Constraint-Induced Movement therapy (CIMT) of persons with impaired lower extremity use from multiple sclerosis (MS). Design: Clinical trial with periodic follow-up for up to 4 years. Setting: University-based rehabilitation research laboratory. Participants: A referred sample of ambulatory adults with chronic MS (N=4) with at least moderate loss of lower extremity use (average item score <= 6.5/10 on the functional performance measure of the Lower Extremity Motor Activity Log [LE-MAL]). Interventions: CIMT was administered for 52.5 hours over 3 consecutive weeks (15 consecutive weekdays) to each patient. Main Outcome Measures: The primary outcome was the LE-MAL score at posttreatment. Secondary outcomes were posttreatment scores on laboratory assessments of maximal lower extremity movement ability. Results: All the patients improved substantially at posttreatment on the LE-MAL, with smaller improvements on the laboratory motor measures. Scores on the LE-MAL continued to improve for 6 months afterward. By 1 year, patients remained on average at posttreatment levels. At 4 years, half of the patients remained above pretreatment levels. There were no adverse events, and fatigue ratings were not significantly changed by the end of treatment. Conclusions: This initial trial of lower extremity CIMT for MS indicates that the treatment can be safely administered, is well tolerated, and produces substantially improved real-world lower extremity use for as long as 4 years afterward. Further trials are needed to determine the consistency of these findings. Archives of Physical Medicine and Rehabilitation 2013;94:753-60 (C) 2013 by the American Congress of Rehabilitation Medicine
引用
收藏
页码:753 / 760
页数:8
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