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临床试验/NCT02325947
NCT02325947已完成不适用

A Multicentre Randomized Single Blind Placebo Controlled Study to Assess Efficacy of Hand Exoskeleton Controlled by Motor Imagery Based BCI for Post Stroke Patients Movement Rehabilitation

Russian Academy of Medical Sciences1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2015年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
75
试验地点
1
主要终点
Change from Baseline in hand paresis level and hand muscle spasticity

研究概览

简要总结

The purpose of this study is to assess the efficacy of non-invasive BCI-exoskeleton technology based on EEG patterns recognition matching to motor imagery in post-stroke patients with hand paresis.

详细描述

The BCI training is based on EEG activity patterns recording during hand motor imagery. A subject sit comfortably 1m from a computer screen which presents visual instructions during the session. The robotic exoskeleton is fixed to the paretic hand. Subject visually fixate on a circle presented in the center of the screen and receive instructions from three surrounding rhomboidal arrows. Subject is given three commands instructing them to relax or imagine slow hand opening movement with the right or left hand. The "Relax" command means that the subject have to sit still and look at the center of the screen. Commands are presented randomly, each of 10 sec duration.

A visual cue provides the subject with feedback regarding the mental task recognition: the central circle turned green if the classifier recognizes the task in agreement with the given command, or remains white if the signal is not recognized. In addition to visual feedback the subject is provided with kinesthetic feedback: the exoskeleton is opening the hand when the classifier recognizes the imagery of paretic hand movement.

The EEG is registered with 30 electrodes distributed over the head in accordance with the standard international 10-20 system. EEG signals are filtered from 5-30Hz. A Bayesian approach for EEG pattern classifying is used in the system. The activity sources most relevant for BCI functioning will be identified using an independent component analysis (ICA). Classification accuracy will by measured with Cohen's kappa (Kohavi and Provost, 1998). The procedure may consist from up to three sessions, the duration of 1 session is 10 min, there are 5 min time brake between session and total duration of procedure is up to 45 min. The number of procedures - at least 10. The maximal interval between procedures is 3 days.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Participant)

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
否

入选标准

  • •Signed informed consent
  • •Medical history of primary acute cerebrovascular event (ischemic or hemorrhagic stroke) at least 4 weeks before screening
  • •focal stroke located in a hemisphere
  • •post stroke hand paresis (mild to plegia according to Medical Research Council (MRC) Scale for Muscle Strength)

排除标准

  • •Montreal Cognitive Assessment (MoCA) scale < 22
  • •Left handedness
  • •Sensory aphasia
  • •Severe impairment of vision
  • •Modified Ashworth Scale (MAS) ≥ 4

研究组 & 干预措施

Study group

Experimental

Hand exoskeleton, brain-computer interface (BCI) 10 sessions of 45-minutes

干预措施: hand exoskeleton, brain-computer interface (BCI), (Device)

Placebo group

Sham Comparator

Hand exoskeleton, sham BCI 10 sessions of 45-minutes (BCI imitation)

干预措施: hand exoskeleton, sham BCI (Device)

结局指标

主要结局

Change from Baseline in hand paresis level and hand muscle spasticity

时间窗: Week 2

ARAT; Fugl-Meyer, Modified Ashworth scale

次要结局

  • Long-term changes from Baseline in hand paresis level and hand muscle spasticity(week 4, week 12, week 24)

研究者

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

Roman Lyukmanov

Research scientist

Russian Academy of Medical Sciences

研究点 (1)

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