Immersive Virtual Reality for Stroke Motor Rehabilitation

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-02-28

Study Completion Date

2015-11-30

Brief Summary

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The present study aims at investigating (i) the feasibility in chronic stroke of using a dedicated virtual reality (VR) based system that embeds real-time 3D motion capture and embodied visual feedback to deliver functional exercises designed for training of impaired upper limb motor skills, (ii) whether chronic stroke survivors improve in functional outcomes in the upper limb when exposed to intensive VR-based therapy, and (iii) safety and tolerance to such a technology. The investigators hypothesize that intensive VR-based rehabilitation may lead to high rehabilitation doses and functional improvement in chronic stroke.

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Detailed Description

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Conditions

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Chronic Stroke Motor Disorders

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Study Groups

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MindMotion PRO

The training sessions consist of virtual reality based rehabilitation exercises using the MindMotion PRO device.

Group Type EXPERIMENTAL

MindMotion PRO

Intervention Type DEVICE

Patients will receive five weeks of therapy with 2 sessions (minimum) per week lasting for 45-60 minutes each minimum. The training sessions are based on the MindMotion PRO's virtual reality exercises.

Interventions

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MindMotion PRO

Patients will receive five weeks of therapy with 2 sessions (minimum) per week lasting for 45-60 minutes each minimum. The training sessions are based on the MindMotion PRO's virtual reality exercises.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Ischemic or hemorrhagic minor-to-moderate (0\<NIHSS\<16) stroke with hemiparesis and experiencing arm motor difficulties
* At least 6 months after stroke incident
* Maximum 4 on the Medical Research Council Scale (MRCS) for shoulder elevation and elbow flexion/extension
* 18 years and older
* First ever stroke

Exclusion Criteria

* Participating in another movement treatment study at the time of the present study
* Severe cognitive impairment (Mini Mental Status Examination score \< 18 points)
* Orthopedic impairment or visual disorders limiting the treatment
* Unable to give informed consent form
* Risk of epileptic seizures

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No