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Clinical application of a robotic ankle training program for cerebral palsy compared to the research laboratory application: Does it translate to practice?

机译:与研究实验室应用相比,针对脑瘫的机器人踝关节训练计划的临床应用:转化为实践吗?

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Objective To determine the clinical efficacy of an ankle robotic rehabilitation protocol for patients with cerebral palsy. Design The clinic cohort was identified from a retrospective chart review in a before-after intervention trial design and compared with a previously published prospective research cohort. Setting Rehabilitation hospital. Participants Children (N=28; mean age, 8.2±3.62y) with Gross Motor Function Classification System levels I, II, or III who were referred for ankle stretching and strengthening used a robotic ankle device in a clinic setting. Clinic results were compared with a previously published cohort of participants (N=12; mean age, 7.8±2.91y) seen in a research laboratory-based intervention protocol. Interventions Patients in the clinic cohort were seen 2 times per week for 75-minute sessions for a total of 6 weeks. The first 30 minutes of the session were spent using the robotic ankle device for ankle stretching and strengthening, and the remaining 45 minutes were spent on functional movement activities. There was no control group. Main Outcome Measures We compared pre- and postintervention measures of plantarflexor and dorsiflexor range of motion, strength, spasticity, mobility (Timed Up and Go test, 6-minute walk test, 10-m walk test), balance (Pediatric Balance Scale), Selective Control Assessment of the Lower Extremity (SCALE), and gross motor function measure (GMFM). Results Significant improvements were found for the clinic cohort in all main outcome measures except for the GMFM. These improvements were equivalent to those reported in the research cohort, except for larger SCALE test changes in the research cohort. Conclusions These findings suggest that translation of repetitive, goal-directed biofeedback training into the clinic setting is both feasible and beneficial for patients with cerebral palsy.
机译:目的确定踝部机器人康复方案对脑瘫患者的临床疗效。设计临床队列是从一项干预前后设计中的回顾性图表审查中确定的,并与先前发表的前瞻性研究队列进行了比较。设置康复医院。参加者具有大腿运动功能分类系统级别I,II或III的儿童(N = 28;平均年龄,8.2±3.62y),他们被要求进行踝关节拉伸和加强训练,并在临床环境中使用了机器人踝关节装置。将临床结果与基于研究实验室的干预方案中先前公布的一组参与者(N = 12;平均年龄,7.8±2.91y)进行比较。干预措施每周两次在临床队列中观察患者75分钟,共6周。训练的前30分钟是使用机器人脚踝装置进行踝部拉伸和加固,其余45分钟用于功能性运动活动。没有对照组。主要结果指标我们比较了干预前后足底屈肌和背屈肌的运动范围,强度,痉挛,活动性(定时跑,6分钟步行测试,10米步行测试),平衡(小儿平衡秤),下肢的选择性控制评估(SCALE)和大运动功能测量(GMFM)。结果除GMFM外,在所有主要结局指标中,临床队列均获得了显着改善。这些改进与研究队列中报告的相同,只是研究队列中的SCALE测试变化较大。结论这些发现表明,将重复的,针对目标的生物反馈训练转换为临床环境对脑瘫患者既可行又有益。

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