Home-based Non-invasive Brain Stimulation and Hand Tracking Rehabilitation for People With Chronic Stroke
2019年5月9日 更新者：University of Minnesota
Home-based tDCS and Hand Tracking Rehabilitation for Chronic Stroke
This is a device feasibility study, which will assess telerehabilitation in people with chronic stroke using a combination of noninvasive brain stimulation and finger tracking training.
Telerehabilitation allows patients to train in their own home which also allows for longer training periods than what is currently allowed clinically.
Noninvasive transcranial direct current stimulation (tDCS) uses two surface electrodes connected to a small battery that will be attached to the head.
This will be used to modulate neuronal excitability.
With sensors attached to fingers and the wrist, the patient will move the joints to track a target displayed on a screen.
The combined treatment will be applied in two experiments.
The first will be on 3 patients coming to our lab and the second on 3 patients in their home, both under supervision.
We will integrate the two components and test the resulting and novel treatment system for technical feasibility, which will set the stage for future efficacy studies under federal grant support.
We hypothesize that the developed system will be safe and feasible.
研究概览
详细说明
This study will assess the feasibility of a telerehabilitation protocol involving non-invasive brain stimulation.
Therefore, the two arms of the study are 1) implementation of this protocol in a controlled laboratory setting and 2) implementation of this protocol in a patient's home, being set up by the patient but controlled remotely using a blue-tooth system by an investigator in a different location.
The two arms of this study will occur successively with the first arm being completed with three patients followed by the second arm being completed with a second group of three patients.
研究类型
介入性
注册 (实际的)
6
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
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Minnesota
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Minneapolis、Minnesota、美国、55455
- University of Minnesota
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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 及以上 (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:
- adult at least 18 years old
- stroke duration >6 months,
- Mini-Mental State Examination score 24 or higher
- presence of tactile sensation on the scalp
- at least 10 degrees of active finger or wrist motion in the stroke hand
- ability to walk 100 feet and transfer independently
Exclusion Criteria:
- seizure within past two years
- pregnancy
- metal inside the had (dental metal is permitted)
- implanted medical devices incompatible with tDCS
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：设备可行性
- 分配：非随机化
- 介入模型：单组作业
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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有源比较器：In-lab tDCS
Three people with chronic stroke will participate in finger tracking training while receiving transcranial direct current stimulation (tDCS) in a controlled laboratory environment with an investigator.
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Transcranial direct current stimulation (tDCS) uses two surface electrodes placed on the scalp.
These electrodes pass a low voltage current and modulate membrane potentials of underlying neurons.
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实验性的：In-home tDCS
Three people with chronic stroke will participate in finger tracking training while receiving transcranial direct current stimulation (tDCS) in their own home.
Patients will be taught how to use a blue-tooth enabled telerehabilitation module that is being controlled by an investigator in the lab on the University campus.
For safety, an investigator will be in the home with each patient during tDCS use and finger tracking training but will only be supervising procedures.
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Transcranial direct current stimulation (tDCS) uses two surface electrodes placed on the scalp.
These electrodes pass a low voltage current and modulate membrane potentials of underlying neurons.
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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 |
|---|---|---|
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Digit Span
大体时间：First day of study and one day following the final treatment
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Short-term memory test using single numerical digits
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First day of study and one day following the final treatment
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Box and block
大体时间：First day of study and one day following the final treatment
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Finger dexterity test using both paretic and nonparetic hands
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First day of study and one day following the final treatment
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Quantification of Compliance Questionnaire
大体时间：First day of study and one day following the final treatment
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First day of study and one day following the final treatment
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User perception survey
大体时间：First day of study and one day following the final treatment
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Survey
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First day of study and one day following the final treatment
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次要结果测量
结果测量 |
大体时间 |
|---|---|
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Survey of symptoms questionnaire
大体时间：Each day of study as well as one day following the final treatment
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Each day of study as well as one day following the final treatment
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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：James Carey, PhD, PT、University of Minnesota
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 (实际的)
2017年1月1日
初级完成 (实际的)
2017年5月1日
研究完成 (实际的)
2017年5月1日
研究注册日期
首次提交
2015年5月29日
首先提交符合 QC 标准的
2015年5月29日
首次发布 (估计)
2015年6月2日
研究记录更新
最后更新发布 (实际的)
2019年5月13日
上次提交的符合 QC 标准的更新
2019年5月9日
最后验证
2019年5月1日
更多信息
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.