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临床试验/NCT02539914
NCT02539914已完成不适用

Interactive System for Diagnostics and Rehabilitation of Cognitive-motor Deficits: Controlled Longitudinal Clinical Study With Stroke Patients

Universidade da Madeira2 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2015年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
18
试验地点
2
主要终点
Change from baseline in the Fugl-Meyer Assessment Test (upper extremity)

研究概览

简要总结

The purpose of this study is to determine whether it is feasible to use a virtual reality task for stroke rehabilitation for training motor and cognitive (attention and memory) domains based on the use of positive stimuli, and to evaluate the potential benefits in comparison to standard rehabilitation.

详细描述

There is evidence that positive emotion stimuli can lead to improved performance in attention tasks and the investigators aim to understand the benefits of using this principle in cognitive and upper-limb motor rehabilitation following stroke. For this purpose, the investigators developed a VR attention task in which the user has to find a target image within a variable number of distractors by controlling a virtual arm. In some levels of the task the target has to be memorized, hence training both attention and memory. The target stimuli are positive images based on the individual preferences of each user.

40 participants within the first 6 months after stroke will be randomly allocated to one of two groups: 1) VR motor-cognitive task or 2) standard rehabilitation. The VR motor-cognitive task group will use the above described virtual task customized to each user in terms of the positive content. This also includes selected music that will be introduced in half of the sessions. The standard rehabilitation group will undergo conventional motor and cognitive rehabilitation. The intervention consists of 12 sessions of 45 minutes administered within a 4-6 weeks period. The participants will be evaluated using a number motor and cognitive assessment scales at baseline, end of the intervention and a 1-month follow-up.

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
None

入排标准

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

入选标准

  • ischemic or hemorrhagic stroke within the first 6 months post-stroke
  • motor impairment of the upper extremity but with a minimum score of 28 in the Motricity Index (elbow flexion and shoulder abduction domains combined score)
  • cognitive deficit but with enough capacity to understand the task and follow instructions with a minimum score of 11 over 17 in the Token Test (6-item version, portuguese population)
  • able to read

排除标准

  • previous motor and/or cognitive deficits
  • normal cognitive functioning with a score above 26 points in the Montreal Cognitive Assessment
  • unilateral spatial neglect
  • moderate to severe depressive symptomatology with a score above 20 points in the Geriatric Depression Scale
  • vision disorders that may interfere with the execution of the task

结局指标

主要结局

Change from baseline in the Fugl-Meyer Assessment Test (upper extremity)

时间窗: Baseline, End (4-6 weeks) and 4-weeks follow-up

Assessment of change from baseline in motor and joint functioning of the paretic upper extremity.

Change form baseline in the Chedoke Arm and Hand Activity Inventory

时间窗: Baseline, End (4-6 weeks) and 4-weeks follow-up

Assessment of change from baseline in the functionality of the paretic upper extremity.

Change from baseline in the Montreal Cognitive Assessment

时间窗: Baseline, End (4-6 weeks) and 4-weeks follow-up

Assessment of change from baseline in cognitive domains: attention and concentration, executive functions, memory, language, visuoconstructional skills, conceptual thinking, calculations, and orientation.

次要结局

  • Change from baseline in the Modified Ashworth Scale(Baseline, End (4-6 weeks) and 4-weeks follow-up)
  • Change from baseline in cancellation tests (single letter, number, bells)(Baseline, End (4-6 weeks) and 4-weeks follow-up)
  • Change from baseline in the Barthel Index(Baseline, End (4-6 weeks) and 4-weeks follow-up)
  • Change from baseline in the Motricity Index (upper extremity)(Baseline, End (4-6 weeks) and 4-weeks follow-up)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sergi Bermúdez i Badia

Professor Auxiliar

Universidade da Madeira

研究点 (2)

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