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Efficacy of Hand Exoskeleton Controlled by BCI in Post Stroke Patients

NCT02325947 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2017-09-29

No results posted yet for this study

Summary

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.

Conditions

  • Poststroke/CVA Paresis

Interventions

DEVICE

hand exoskeleton, brain-computer interface (BCI),

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

DEVICE

hand exoskeleton, sham BCI

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

Sponsors & Collaborators

  • Pirogov Russian National Research Medical University

    collaborator OTHER

  • Russian Academy of Medical Sciences

    lead OTHER

Principal Investigators

  • Roman Lyukmanov, MD · Russian Academy of Medical Sciences

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2017-09-30
Completion
2017-09-30

Countries

  • Russia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02325947 on ClinicalTrials.gov