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首页> 外文期刊>Journal of Rehabilitation Research and Development >Robot-assisted upper-limb therapy in acute rehabilitation setting following stroke: Department of Veterans Affairs multisite clinical trial
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Robot-assisted upper-limb therapy in acute rehabilitation setting following stroke: Department of Veterans Affairs multisite clinical trial

机译:中风后急性康复环境中机器人辅助的上肢治疗:退伍军人事务部多站点临床试验

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This randomized, controlled, multisite Department of Veterans Affairs clinical trial assessed robotassisted (RA) upperlimb therapy with the Mirror Image Movement Enabler (MIME) in the acute stroke rehabilitation setting. Hemiparetic subjects (n = 54) received RA therapy using MIME for either up to 15 hours (lowdose) or 30 hours (highdose) or received up to 15 hours of additional conventional therapy in addition to usual care (control). The primary outcome measure was the FuglMeyer Assessment (FMA). The secondary outcome measures were the Functional Independence Measure (FIM), Wolf Motor Function Test, Motor Power, and Ashworth scores at intake, discharge, and 6month followup. Mean duration of study treatment was 8.6, 15.8, and 9.4 hours for the lowdose, highdose, and control groups, respectively. Gains in the primary outcome measure were not significantly different between groups at followup. Significant correlations were found at discharge between FMA gains and the dose and intensity of RA. Intensity also correlated with FMA gain at 6 months. The highdose group had greater FIM gains than controls at discharge and greater tone but no difference in FIM changes compared with lowdose subjects at 6 months. As used during acute rehabilitation, motorcontrol changes at followup were no less with MIME than with additional conventional therapy. Intensity of training with MIME was positively correlated with motorcontrol gains.
机译:这项随机,受控,多站点的退伍军人事务部临床试验评估了在急性中风康复环境中使用镜像运动启动器(MIME)进行的机器人辅助(RA)上肢治疗。偏瘫患者(n = 54)接受了使用MIME的RA治疗长达15小时(低剂量)或30小时(高剂量),或者除常规护理外还接受了长达15小时的其他常规治疗(对照)。主要结果指标是FuglMeyer评估(FMA)。次要结局指标为功能独立性指标(FIM),狼运动功能测试,运动功率和入院,出院及6个月随访时的Ashworth评分。低剂量组,高剂量组和对照组的平均研究治疗时间分别为8.6、15.8和9.4小时。随访时各组间主要结局指标的获益无显着差异。出院时发现FMA增高与RA的剂量和强度之间存在显着相关性。强度也与6个月时的FMA增加相关。高剂量组在出院时比对照组具有更大的FIM增益,并且音调更大,但与6个月低剂量组相比,FIM变化无差异。正如在急性康复中使用的那样,MIME随访时的运动控制改变与其他常规疗法相当。 MIME的训练强度与运动控制增益呈正相关。

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