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临床试验/NCT03666533
NCT03666533已完成不适用

Transcranial Direct Current Stimulation for Post-stroke Gait Rehab

VA Office of Research and Development2 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2018年9月13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
44
试验地点
2
主要终点
Change in Gait Speed From Baseline (Meters/Second)

研究概览

简要总结

Stroke affects upwards of 800,000 Americans every year and has an enormous impact on the well-being of the American Veteran population with 6,000 new stroke admissions every year. Many of these stroke survivors are living with walking disabilities. Gait problems result in inability to function independently, high risk of falls and poor quality of life. Unfortunately, current gait rehabilitation treatments are limited and many stroke survivors do not achieve full recovery. Therefore, it is critical to develop new approaches to enhance gait rehabilitation methods. The investigators propose to evaluate a brain stimulation treatment called transcranial Direct Current Stimulation (tDCS) that can be added to physical therapy. tDCS has been applied for arm rehabilitation after stroke with positive results, but gait-related investigations are lacking. The investigators will test whether simultaneous tDCS and gait training produces greater improvement in walking abilities than gait training alone. Adjunct tDCS therapy may improve outcomes, and reduce cost of both rehabilitation and post-stroke care.

详细描述

Current rehabilitation methods fail to restore normal gait for many stroke survivors leading to dependence on others, recurrent falls, limitations in community ambulation and poor quality of life. The main objective of this study is to test both efficacy and neurophysiological mechanisms of a novel approach to treat persistent gait deficits after stroke with a combination of simultaneous non-invasive brain stimulation with transcranial Direct Current Stimulation (tDCS) and gait training. The investigators will enroll chronic stroke subjects (>6 months) with gait deficits. Subjects will be randomized to 10 sessions of either active tDCS+gait training or sham tDCS+gait training. Gait training will be accomplished in the treadmill-based Virtual Reality environment targeting longer single limb stance with the paretic limb. The primary outcome measure will be both gait speed and single limb stance duration. Other outcome measures will assess various components of gait-related functional domains. The study will also characterize neuroplastic brain changes in response to bihemispheric tDCS combined with gait training based on corticospinal excitability using motor evoked potentials and functional connectivity using resting state functional Magnetic Resonance Imaging (rs-fMRI).

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • Medically and psychologically stable and at least 6 months after first ever unilateral stroke
  • Cognition sufficiently intact to give valid informed consent to participate
  • FMLE score >15; and ability to actively dorsiflex the paretic ankle in synergy (FMLE item II Flexor synergy-ankle dorsiflexion score 1).
  • Sufficient endurance to participate in the study

排除标准

  • Activity tolerance is insufficient to complete treadmill training
  • Inability to produce a trace contraction of ankle dorsiflexors in synergy
  • Normal ankle dorsiflexion/knee flexion on FMLE standing items (FMLE item IV score=4)
  • Stroke affecting both sides
  • Contraindications for rTMS according to the most recent TMS-use guidelines
  • Contraindications for MRI
  • Inability to understand English

结局指标

主要结局

Change in Gait Speed From Baseline (Meters/Second)

时间窗: baseline to post treatment (after 5 weeks of treatment)

Gait speed will be calculated based on Ten Meter Walk Test

次要结局

  • Change From Baseline to Post Treatment on Timed up and go (Seconds)(baseline to post treatment (after 5 weeks of treatment))
  • Change From Baseline to Post Treatment in Functional Gait Assessment (Points)(baseline to post treatment (after 5 weeks of treatment))
  • Change From Baseline to Post Treatment on Fugl Meyer Lower Limb(baseline to post treatment (after 5 weeks of treatment))
  • Change From Baseline to Post Treatment on Gait Assessment and Intervention Tool(baseline to post treatment (after 5 weeks of treatment))
  • Change From Baseline to Post Treatment on Timed up and go (Seconds)(baseline to post treatment (after 5 weeks of treatment))
  • Change From Baseline to Post Treatment in Functional Gait Assessment (Points)(baseline to post treatment (after 5 weeks of treatment))
  • Change From Baseline to Post Treatment on Fugl Meyer Lower Limb(baseline to post treatment (after 5 weeks of treatment))
  • Change From Baseline to Post Treatment on Gait Assessment and Intervention Tool(baseline to post treatment (after 5 weeks of treatment))
  • Change in Asymmetry of Tibialis Anterior Muscle Motor Evoked Potentials From Baseline(baseline to after 5 weeks of treatment)

研究者

申办方类型
Fed
责任方
Sponsor

研究点 (2)

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