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Individual finger synchronized robot-assisted hand rehabilitation in subacute to chronic stroke: A prospective randomized clinical trial of efficacy

机译:亚急性慢性卒中的个体手指同步机器人辅助手康复:一项前瞻性随机临床疗效试验

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Objective: To evaluate individual finger synchronized robot-assisted hand rehabilitation in stroke patients. Design: Prospective parallel group randomized controlled clinical trial. Subjects: The study recruited patients who were ≥18 years old, more than three months post stroke, showed limited index finger movement and had weakened and impaired hand function. Patients with severe sensory loss, spasticity, apraxia, aphasia, disabling hand disease, impaired consciousness or depression were excluded. Interventions: Patients received either four weeks (20 sessions) of active robot-assisted intervention (the FTI (full-term intervention) group, 9 patients) or two weeks (10 sessions) of early passive therapy followed by two weeks (10 sessions) of active robot-assisted intervention (the HTI (half-term intervention) group, 8 patients). Patients underwent arm function assessments prior to therapy (baseline), and at 2, 4 and 8 weeks after starting therapy. Results: Compared to baseline, both the FTI and HTI groups showed improved results for the Jebsen Taylor test, the wrist and hand subportion of the Fugl-Meyer arm motor scale, active movement of the 2nd metacarpophalangeal joint, grasping, and pinching power (P < 0.05 for all) at each time point (2, 4 and 8 weeks), with a greater degree of improvement for the FTI compared to the HTI group (P < 0.05); for example, in Jebsen Taylor test (65.9 ± 36.5 vs. 46.4 ± 37.4) and wrist and hand subportion of the Fugl- Meyer arm motor scale (4.3 ± 1.9 vs. 3.4 ± 2.5) after eight weeks. Conclusions: A four-week rehabilitation using a novel robot that provides individual finger synchronization resulted in a dose-dependent improvement in hand function in subacute to chronic stroke patients.
机译:目的:评估中风患者的单指同步机器人辅助手康复。设计:前瞻性平行组随机对照临床试验。受试者:该研究招募了≥18岁,卒中后三个月以上,食指运动受限,手功能减弱和受损的患者。排除严重感觉丧失,痉挛,失语,失语,手部残疾,意识障碍或抑郁的患者。干预措施:患者接受了四周(20节)的主动机器人辅助干预(FTI(足月干预)组,九名患者)或两周(10堂)的早期被动治疗,然后接受了两周(10堂)机器人辅助主动干预(HTI(半期干预)组,8例患者)。患者在治疗前(基线)以及开始治疗后的第2、4和8周接受手臂功能评估。结果:与基线相比,FTI和HTI组的Jebsen Taylor试验,Fugl-Meyer臂运动量表的腕部和手部,第2掌指关节的活动,抓握和捏捏力​​(P在每个时间点(2、4和8周)均<0.05),与HTI组相比,FTI的改善程度更大(P <0.05);例如,在Jebsen Taylor测试中(65.9±36.5 vs. 46.4±37.4)以及Fugl-Meyer手臂运动量表的手腕和手部分(八周后为4.3±1.9 vs. 3.4±2.5)。结论:使用提供个体手指同步功能的新型机器人进行了为期四周的康复,导致亚急性慢性卒中患者的手部功能呈剂量依赖性改善。

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