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首页> 外文期刊>JAMA: the Journal of the American Medical Association >Effect of constraint-induced movement therapy on upper extremity function 3 to 9 months after stroke: the EXCITE randomized clinical trial.
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Effect of constraint-induced movement therapy on upper extremity function 3 to 9 months after stroke: the EXCITE randomized clinical trial.

机译:约束诱发的运动疗法对卒中后3至9个月的上肢功能的影响:EXCITE随机临床试验。

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CONTEXT: Single-site studies suggest that a 2-week program of constraint-induced movement therapy (CIMT) for patients more than 1 year after stroke who maintain some hand and wrist movement can improve upper extremity function that persists for at least 1 year. OBJECTIVE: To compare the effects of a 2-week multisite program of CIMT vs usual and customary care on improvement in upper extremity function among patients who had a first stroke within the previous 3 to 9 months. DESIGN AND SETTING: The Extremity Constraint Induced Therapy Evaluation (EXCITE) trial, a prospective, single-blind, randomized, multisite clinical trial conducted at 7 US academic institutions between January 2001 and January 2003. PARTICIPANTS: Two hundred twenty-two individuals with predominantly ischemic stroke. INTERVENTIONS: Participants were assigned to receive either CIMT (n = 106; wearing a restraining mitt on the less-affected hand while engaging in repetitive task practice and behavioral shaping with the hemiplegic hand) or usual and customary care (n = 116; ranging from no treatment after concluding formal rehabilitation to pharmacologic or physiotherapeutic interventions); patients were stratified by sex, prestroke dominant side, side of stroke, and level of paretic arm function. MAIN OUTCOME MEASURES: The Wolf Motor Function Test (WMFT), a measure of laboratory time and strength-based ability and quality of movement (functional ability), and the Motor Activity Log (MAL), a measure of how well and how often 30 common daily activities are performed. RESULTS: From baseline to 12 months, the CIMT group showed greater improvements than the control group in both the WMFT Performance Time (decrease in mean time from 19.3 seconds to 9.3 seconds [52% reduction] vs from 24.0 seconds to 17.7 seconds [26% reduction]; between-group difference, 34% [95% confidence interval {CI}, 12%-51%]; P<.001) and in the MAL Amount of Use (on a 0-5 scale, increase from 1.21 to 2.13 vs from 1.15 to 1.65; between-group difference, 0.43 [95% CI, 0.05-0.80]; P<.001) and MAL Quality of Movement (on a 0-5 scale, increase from 1.26 to 2.23 vs 1.18 to 1.66; between-group difference, 0.48 [95% CI, 0.13-0.84]; P<.001). The CIMT group achieved a decrease of 19.5 in self-perceived hand function difficulty (Stroke Impact Scale hand domain) vs a decrease of 10.1 for the control group (between-group difference, 9.42 [95% CI, 0.27-18.57]; P=.05). CONCLUSION: Among patients who had a stroke within the previous 3 to 9 months, CIMT produced statistically significant and clinically relevant improvements in arm motor function that persisted for at least 1 year.Trial Registration clinicaltrials.gov Identifier: NCT00057018.
机译:背景:单点研究表明,对于中风后1年以上,保持手部和腕部运动的患者进行为期2周的约束诱发运动疗法(CIMT)方案,可以改善上肢功能,这种功能至少持续1年。目的:比较一项为期2周的CIMT多站点计划与常规和常规护理对前3到9个月内首次中风的患者上肢功能改善的影响。设计与地点:肢体约束诱导疗法评估(EXCITE)试验,这是一项前瞻性,单盲,随机,多站点临床试验,于2001年1月至2003年1月间在美国7家学术机构中进行。缺血性中风。干预措施:参与者被分配为接受CIMT(n = 106;在患病较少的手上戴着约束手套,同时用偏瘫手进行重复性任务练习和行为塑形)或常规和习惯护理(n = 116;范围从在正式接受药理或物理治疗干预后未进行任何治疗);患者按性别,卒中前支配侧,卒中侧和臂突功能水平进行分层。主要观察指标:沃尔夫运动功能测试(WMFT),用于衡量实验室时间和基于力量的能力以及运动质量(功能能力)的度量,以及运动活动日志(MAL),用于度量良好程度和频率30进行日常的日常活动。结果:从基线到12个月,CIMT组在WMFT执行时间上均显示出比对照组更大的改善(平均时间从19.3秒减少到9.3秒[减少52%],而从24.0秒减少到17.7秒[26%]减少];组间差异为34%[95%置信区间{CI},为12%-51%]; P <.001),并且MAL的使用量(以0-5的比例从1.21增加到2.13 vs.1.15至1.65;组间差异0.43 [95%CI,0.05-0.80]; P <.001)和MAL运动质量(0-5级,从1.26至2.23 vs.1.18至1.66 ;组间差异为0.48 [95%CI,0.13-0.84]; P <.001)。 CIMT组的自我感觉手功能难度(卒中影响量表手域)降低了19.5,而对照组则降低了10.1(组间差异为9.42 [95%CI,0.27-18.57]; P = .05)。结论:在前3到9个月内患有中风的患者中,CIMT在手臂运动功能方面具有统计学上显着且与临床相关的改善,至少持续1年。临床注册临床试验.gov标识符:NCT00057018。

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