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A low cost virtual reality system for home based rehabilitation of the arm following stroke: a randomised controlled feasibility trial

机译:一种低成本的虚拟现实系统,用于家庭康复手臂中风:一项随机对照可行性试验

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摘要

Objective udTo assess the feasibility of conducting a randomised controlled trial of a home-based virtual reality system for rehabilitation of the arm following stroke.ududDesignudTwo group feasibility randomised controlled trial of intervention versus usual care.ududSetting udPatients’ homes.ududParticipants udPatients aged 18 or over, with residual arm dysfunction following stroke and, no longer receiving any other intensive rehabilitation.ududInterventionsudEight weeks’ use of a low cost home-based virtual reality system employing infra-red capture to translate the position of the hand into game play or usual care.ududMain measures udThe primary objective was to collect information on the feasibility of a trial, including recruitment, collection of outcome measures and staff support required. Patients were assessed at three time points using the Wolf Motor Function Test, Nine-Hole Peg Test, Motor Activity Log and Nottingham Extended Activities of Daily Living.ududResults udOver 15 months only 47 people were referred to the team. Twenty seven were randomised and 18 (67%) of those completed final outcome measures. Sample size calculation based on data from the Wolf Motor Function Test indicated a requirement for 38 per group. There was a significantly greater change from baseline in the intervention group on midpoint Wolf Grip strength and two subscales of the final Motor Activity Log. Training in the use of the equipment took a median of 230 minutes per patient.ududConclusions To achieve the required sample size, a definitive home-based trial would require additional strategies to boost recruitment rates and adequate resources for patient support.
机译:目的 ud评估进行基于家庭的虚拟现实系统进行卒中后手臂康复的随机对照试验的可行性。 ud udDesign ud两组干预与常规护理的两组可行性随机对照试验。 ud udSetting udPatients的住所。 ud ud参与者 ud18岁或以上的患者,中风后手臂残余功能障碍,不再接受任何其他密集的康复治疗。 ud udInterventions ud八周使用低成本的基于家庭的虚拟现实系统 ud ud主要措施 ud主要目标是收集有关试验可行性的信息,包括招募,收集结果措施和所需的人员支持。使用狼运动功能测试,九孔钉测试,运动活动记录和诺丁汉日常生活扩展活动在三个时间点对患者进行了评估。 ud ud结果 ud超过15个月,只有47人被转介至该团队。 27例患者被随机分组​​,其中18例(67%)完成了最终结局指标。根据来自沃尔夫汽车功能测试的数据进行的样本数量计算表明,每组需要38人。干预组的中点Wolf Grip强度和最终运动活动日志的两个分量表与基线相比有明显更大的变化。每位患者使用该设备的培训平均花费230分钟。 ud ud结论为达到所需的样本量,一项确定的家庭试验需要其他策略来提高招募率和充足的患者支持资源。

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