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临床试验/NCT03502122
NCT03502122已完成不适用

Design and Verification of Individualized Smart Assistive Devices for Stroke Rehabilitation

National Central University, Taiwan0 个研究点目标入组 48 人开始时间: 2012年4月24日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
48
主要终点
Change in FUGL- MEYER ASSESSMENT OF PHYSICAL PERFORMANCE (FMA)

研究概览

简要总结

This study aims to design and verify a multi-mode smart assistive device system for Stroke Rehabilitation by using EEG, fMRI, IMU and questioners

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
20 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • the first time hemiparetic stroke;
  • diagnosis confirmed by a physician on the basis of the findings of neurological examinations and brain imaging (magnetic resonance imaging or computed tomography scan);
  • aged between 20 and 85 years;
  • Brunnstrom's stage II to V over the proximal and distal part of the upper extremity on the affected side;
  • no cognitive dysfunction, measured by the Mini-Mental State Exam (≧24; suggested by 36 with respect to age and educational level)
  • willing/able to participate and having signed an informed consent form.

排除标准

  • unstable vital sign
  • irreversible contracture over any of the joints of the affected upper extremity
  • history of surgery, fracture, arthritis, pain, or any other complications that might influence the recovery of upper extremity function like aphasia, apraxia and neglect;
  • having spasticity, as measured using the Modified Ashworth scale (score > 2);
  • poststroke seizure;
  • heart attack within 3 months poststroke; cortical lesions in any of the five core motor areas of interest, including the bilateral M1, the bilateral PM, and the SMA.

研究组 & 干预措施

VR rehabilitation

Experimental

Virtual Reality based rehabilitation therapy for motor function, 1 hour a time at an intensity of three times per week over 8 weeks (total, 24 sessions).

干预措施: VR rehabilitation for motor function (Other)

control- conventional rehabilitation

Active Comparator

conventional rehabilitation therapy for motor function, 1 hour a time at an intensity of three times per week over 8 weeks (total, 24 sessions).

干预措施: VR rehabilitation for motor function (Other)

结局指标

主要结局

Change in FUGL- MEYER ASSESSMENT OF PHYSICAL PERFORMANCE (FMA)

时间窗: pre, post (after 24 hrs of intervention) and follow-up (one month after finishing intervention )

FUGL- MEYER ASSESSMENT OF PHYSICAL PERFORMANCE (FMA)

次要结局

  • change in upper extremity performance evaluation test for the elderly (TEMPA)(pre, post (after 24 hrs of intervention) and follow-up (one month after finishing intervention ))
  • change in Brunnstrom stage(pre, post (after 24 hrs of intervention) and follow-up (one month after finishing intervention ))
  • change in Wolf motor function(pre, post (after 24 hrs of intervention) and follow-up (one month after finishing intervention ))

研究者

发起方
National Central University, Taiwan
申办方类型
Other
责任方
Principal Investigator
主要研究者

Chun-Chuan Chen

Associate professor

National Central University, Taiwan

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