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临床试验/NCT02586597
NCT02586597已完成不适用

Paired Associative Stimulation Modulates Motor Excitability and Plasticity in Chronic Stroke Patients

Medical University of South Carolina2 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2015年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
17
试验地点
2
主要终点
Intracortical facilitation

研究概览

简要总结

Stroke is the third most common cause of death in the United States after heart disease and cancer, and the leading cause of long-term disability. This work will develop an innovative brain stimulation method (paired associative stimulation) which might set the stage for a new treatment for stroke rehabilitation.

详细描述

Stroke is the third most common cause of death in the United States after heart disease and cancer. An innovative recovery treatment is in demand for stroke motor recovery. Paired associative stimulation (PAS) is a new technique where one pairs a peripheral stimulation with centrally applied transcranial magnetic stimulation (TMS), and produces plasticity, as measured by TMS motor-evoked potentials (MEP's). The investigators will also compare post-stroke patients to healthy controls on the modulation effect of PAS and motor behavior measures.

Aim1. To investigate whether PAS (PAS25 or PAS10) can modulate motor excitability and plasticity;

Aim2. To investigate whether PAS can modify motor behaviors measures in both post-stroke patients and healthy controls;

Aim3. To investigate whether post-stroke patients show different modulation of PAS on both cortical plasticity and motor behavior measure compared to healthy controls.

For this study the investigators will enroll a total of 10 chronic stroke patients and 10 neurologically healthy controls matched for age and gender. Participants will have 4 visits. The first visit is for screening. They will receive either sham PAS or real PAS25 or real PAS10 at each following treatment visit.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Device Feasibility
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18-80 years old;
  • first-ever ischemic stroke involving only one hemisphere;
  • Patient demonstrates at least 10 degrees of voluntary finger, thumb and wrist extension; ;
  • 6 - 24 months after ischemic stroke

排除标准

  • Primary or secondary intracerebral hematoma, or subarachnoid hemorrhage, or subdural/epidural hematoma;
  • Bihemispheric ischemic strokes;
  • History of prior stroke or old infarct demonstrated on the CT or MRI or documented in medical records or current on anticoagulant;
  • Other concomitant neurological disorders, such as brain tumor, abscess or spinal cord disease affecting upper extremity motor function;
  • Documented history of dementia prior to index event;
  • Presence of any MRI/TMS risk factors such as (a) an electrically, magnetically or mechanically activated implant including cardiac pacemaker, intracerebral vascular clips or any other electrically sensitive support system; (b) non-fixed metal in any part of the body, including a previous metallic injury to eye [all jewelry will be removed during stimulation]; (c) pregnancy, since the effect of TMS on the fetus is unknown, females of child bearing age will have to undergo a pregnancy test to confirm eligibility; (d) history of seizure disorder or post-stroke seizures. This last exclusion criterion applies only to the modulation portion of the proposal; (e) median nerve is damaged

结局指标

主要结局

Intracortical facilitation

时间窗: 10-day treatment

the peak magnitude of MEP

次要结局

  • Clinical behavioral measures-Handgrip(10-day treatment)
  • Nine-hole peg test(10-day treatment)
  • wolf motor function test(10-day treatment)

研究者

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

Xingbao Li

Assistant Professor

Medical University of South Carolina

研究点 (2)

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