Effects of Conventional Physical Therapy and Functional Strength Training on Upper Limb Motor Recovery After Stroke: A Randomized Phase II Study

被引:58
作者
Donaldson, Catherine [2 ]
Tallis, Raymond [3 ]
Miller, Simon [2 ]
Sunderland, Alan [4 ]
Lemon, Roger [5 ]
Pomeroy, Valerie [1 ]
机构
[1] Univ E Anglia, Fac Hlth, Norwich NR4 7TJ, Norfolk, England
[2] St Georges Univ London, London, England
[3] Univ Manchester, Stockport, Lancs, England
[4] Univ Nottingham, Sch Psychol, Nottingham NG7 2RD, England
[5] UCL, Inst Neurol, London WC1E 6BT, England
关键词
Stroke rehabilitation; Physical therapy; Clinical trial; Upper extremity hemiplegia; UPPER EXTREMITY FUNCTION; RESEARCH ARM TEST; CONTROLLED-TRIAL; PHYSIOTHERAPY TREATMENT; INCREASED-INTENSITY; MUSCLE STRENGTH; PERFORMANCE; WEAKNESS; PEOPLE; GRIP;
D O I
10.1177/1545968308326635
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Background. Functional training and muscle strength training may improve upper limb motor recovery after stroke. Combining these as functional strength training (FST) might enhance the benefit, but it is unclear whether this is better than conventional physical therapy (CPT). Comparing FST with CPT is not straightforward. Objective. This study aimed at assessing the feasibility of conducting a phase III trial comparing CPT with FST for upper limb recovery. Methods. Randomized, observer-blind, phase II trial. Subjects had upper limb weakness within 3 months of anterior circulation infarction. Subjects were randomized to CPT (no extra therapy), CPT+CPT, and CPT+ FST. Intervention lasted 6 weeks. Primary outcome measure was the Action Research Arm Test (ARAT). Measurements were taken before treatment began, after 6 weeks of intervention, and 12 weeks thereafter. Attrition rate was calculated and differences between groups were interpreted using descriptive statistics. ARAT data were used to inform a power calculation. Results. Thirty subjects were recruited (8% of people screened). Attrition rate was 6.7% at outcome and 40% at follow-up. At outcome the CPT+FST group showed the largest increase in ARAT score and this was above the clinically important level of 5.7 points. Median (interquartile range) increases were 11.5 (21.0) for CPT; 8.0 (13.3) for CPT+CPT; and 19.5 (22.0) for CPT+FST. The estimated sample size for an adequately powered subsequent phase III trial was 279 subjects at outcome. Conclusion. Further work toward a phase III clinical trial appears justifiable.
引用
收藏
页码:389 / 397
页数:9
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