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临床试验/NCT01127789
NCT01127789撤回1 期

The Use of Transcranial Direct Current Stimulation (tDCS) to Study Implicit Motor Learning on Patients With Brain Injury

National Taiwan University Hospital2 个研究点 分布在 1 个国家开始时间: 2010年3月最近更新:
适应症

试验速览

阶段
1 期
状态
撤回
试验地点
2
主要终点
Reaction time (millisecond)

研究概览

简要总结

The purpose of this study is to study motor learning and recovery of patients with brain damage caused by traumatic brain injury or stroke with transcranial direct current stimulation (tDCS). It is hypothesized that anodal tDCS on the lesion side and/or cathodal tDCS on the healthy side of motor cortex could improve the recovery of motor function such as learning.

详细描述

We aim to apply transcranial direct current stimulation (tDCS) to study the recovery process of motor learning on the patients with brain damage caused by traumatic brain injury or stroke. Both anodal and cathodal tDCS will be used to test whether the increase of motor cortical activity by anodal tDCS over lesional side or the decrease of brain activity by cathodal tDCS on healthy side will improve the learning skill (SRTT: serial reaction time task). The result could help to understand the mechanism of motor and cognitive recovery after brain damage, and further rationalize the application of non-invasive brain stimulation such as tDCS for patient rehabilitation.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • TBI or stroke patients
  • with partially preserved fine motor function

排除标准

  • with metal clips in head or device (e.g. pacemaker)
  • with active CNS drugs

结局指标

主要结局

Reaction time (millisecond)

时间窗: 24 hours post intervention

Primary outcome measure is the average reaction time of 360 trials from each block -- the task is composed of 8 blocks. After intervention, 3 blocks will be re-tested for 3 times to evaluate the consolidating effect of tDCS on motor learning.

次要结局

  • Error rate (percentage)(24 hours post intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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