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临床试验/NCT02308852
NCT02308852暂停不适用

Improving Bi-manual Activities in Stroke Patients With Application of Neuro-stimulation

University Hospital of Mont-Godinne2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2014年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
暂停
发起方
入组人数
100
试验地点
2
主要终点
bimanual coordination

研究概览

简要总结

Noninvasive brain stimulations (NIBS) will be used in healthy volunteers and in chronic stroke patients to improve bimanual activities and motor learning.

Functional magnetic resonance imaging will be used to evaluate the mechanisms underlying bimanual activities and motor learning in healthy volunteers and in chronic stroke patients.

A neuro-rehabilitation robot (REA2PLAN, AXINESIS, Louvain-la-Neuve, Belgium) will be used for motor learning.

详细描述

tDCS will be used in a sham-controlled, double-blind, randomized, cross-over control trial in chronic stroke patients with motor deficits. After informed consent and recruitment, patients will be randomly (computer method) allocated to real or sham tDCS, that will be applied during performance of bimanual activities and/or motor learning. A few minutes/hours/days/weeks after completing one trial's arm, the patients will enter the other trial's arm (double-blind cross-over design).

Baseline and follow-up outcomes about bimanual and unimanual motor tasks will be collected.

For a subset of subjects, motor learning and data acquisition will be performed with a neuro-rehabilitation robot (REA2PLAN, AXINESIS, Louvain-la-Neuve, Belgium) .

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 95 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • stroke with at least slight deficit

排除标准

  • contraindication to tDCS and/or to fMRI
  • presence of metal in the head
  • inability to understand / complete behavioral tasks
  • chronic intake of alcohol or recreational drugs
  • major health condition
  • presence of pacemaker (for the fMRI part only)
  • pregnancy

结局指标

主要结局

bimanual coordination

时间窗: up to 2 hours after intervention. Recall test at 1 week and up to,2,3,4 weeks after the intervention

The effect of intervention on bimanual motor coordination will be quantified before, during and after executive tasks.

次要结局

  • standard unimanual evaluation(immediately, 30, 60 min; and up to 2 hours after intervention. Recall test at 1 week and up to,2,3,4 weeks after the intervention))

研究者

发起方
University Hospital of Mont-Godinne
申办方类型
Other
责任方
Principal Investigator
主要研究者

Pr Yves Vandermeeren, MD, PhD

Professer Yves Vandermeeren

University Hospital of Mont-Godinne

研究点 (2)

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