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Interactive Intention-Driven Upper-Limb Training Robotic System

2017年2月23日 更新者:Raymond KY Tong、The Hong Kong Polytechnic University

Trial: Interactive Intention-Driven Upper-Limb Training Robotic System

The goal of this study is to determine robotic hand system is more effective than conventional physical and occupational therapy at promoting functional recovery of the affected arm in subjects after stroke.

研究概览

详细说明

This study will investigate the recovery in hand and upper limb functions when the physical training is assisted by an exoskeleton robotic hand system.

Subjects with a pure unilateral motor paresis after a stroke (ischemic or hemorrhagic). All subjects should have sufficient cognition to follow simple instructions as well as understand the content and purpose of the experiment, and also should be able to sit up for 1 hour.

During the training, you will be asked to do the hand open and hand grasp by Electromyography-driven robotic control strategy.

There will be evaluations on the upper limb motor functions before and after the 20-session of training and follow up session by clinical assessments on functional recovery.

研究类型

介入性

注册 (预期的)

70

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Hong Kong、香港
        • The Hong Kong Polytechnic University

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 100年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Subjects with a pure unilateral motor paresis after a stroke (ischemic or hemorrhagic). All subjects should have sufficient cognition to follow simple instructions as well as understand the content and purpose of the experiment, and also should be able to sit up for 1 hour.

Exclusion Criteria:

  • Excessive spasticity of the affected arm
  • Participation in any therapeutic treatment ("outside therapy") performed with the paralyzed arm during the planned study - including baseline and follow up.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Hand Robotic Training
Training for 20 sessions for one hour, 3-5 times per week.
实验性的:Hand and Arm Robotic Training
Training for 20 sessions for one hour, 3-5 times per week.
有源比较器:常规疗法
Training for 20 sessions for one hour, 3-5 times per week.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Fugl-Meyer Assessment
大体时间:Change from baseline Fugl-Meyer Assessment at the end of intervention, at three months and at six months

Evaluate the change from baseline assessment at the end of intervention and monitor the continuous change at three months and six months.

Baseline assessment will be conducted at within one week prior to intervention. Participants will be followed for the duration of hospital stay, an expected average of 5 weeks for the 20-session intervention. The assessment at the end of intervention will be conducted within one week after the intervention. The other two assessments will be conducted at three months and six months after the last session of the intervention.

Change from baseline Fugl-Meyer Assessment at the end of intervention, at three months and at six months
Action Research Arm Test
大体时间:Change from baseline Action Research Arm Test at the end of intervention, at three months and at six months

Evaluate the change from baseline test at the end of intervention and monitor the continuous change at three months and six months.

Baseline test will be conducted at within one week prior to intervention. Participants will be followed for the duration of hospital stay, an expected average of 5 weeks for the 20-session intervention. The assessment at the end of intervention will be conducted within one week after the intervention. The other two assessments will be conducted at three months and six months after the last session of the intervention.

Change from baseline Action Research Arm Test at the end of intervention, at three months and at six months

次要结果测量

结果测量
措施说明
大体时间
Wolf Motor Function Test
大体时间:Change from baseline Wolf Motor Function Test at the end of intervention, at three months and at six months

Evaluate the change from baseline test at the end of intervention and monitor the continuous change at three months and six months.

Baseline test will be conducted at within one week prior to intervention. Participants will be followed for the duration of hospital stay, an expected average of 5 weeks for the 20-session intervention. The assessment at the end of intervention will be conducted within one week after the intervention. The other two assessments will be conducted at three months and six months after the last session of the intervention.

Change from baseline Wolf Motor Function Test at the end of intervention, at three months and at six months
modified Ashworth Scale
大体时间:Change from baseline modified Ashworth Scale at the end of intervention, at three months and at six months

Evaluate the change from baseline test at the end of intervention and monitor the continuous change at three months and six months.

Baseline test will be conducted at within one week prior to intervention. Participants will be followed for the duration of hospital stay, an expected average of 5 weeks for the 20-session intervention. The assessment at the end of intervention will be conducted within one week after the intervention. The other two assessments will be conducted at three months and six months after the last session of the intervention.

Change from baseline modified Ashworth Scale at the end of intervention, at three months and at six months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Raymond KY Tong, PhD、The Hong Kong Polytechnic University

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2014年1月1日

初级完成 (实际的)

2015年12月31日

研究完成 (实际的)

2016年12月31日

研究注册日期

首次提交

2014年2月27日

首先提交符合 QC 标准的

2014年3月3日

首次发布 (估计)

2014年3月4日

研究记录更新

最后更新发布 (实际的)

2017年2月24日

上次提交的符合 QC 标准的更新

2017年2月23日

最后验证

2017年2月1日

更多信息

与本研究相关的术语

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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