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Virtual reality rehab: stroke patients try App-Based recovery at home

NCT ID NCT06885502

Symptom relief Sponsor: Eodyne Systems SL Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests a smartphone app that uses virtual and augmented reality to help people who had a stroke improve arm movement and thinking skills from home. Seventy chronic stroke patients will either use the app or receive standard care for six weeks. The main goal is to see if the app improves arm function better than usual therapy.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 70 people

The number the study aims to enrol. It can still change while the study runs.

Started

Feb 2025

Expected to finish

Jun 2026

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patients presenting an ischemic or intracerebral haemorrhagic stroke, ≥ 3 months post-stroke. * Age \> 18 years old * Moderate to mild proximal upper limb motor impairment Medical Research Council Scale (MRC \>2). * ARAT: \<50, inclusive, to avoid ceiling effects while allowing room for improvement. * Able to sit on a chair or a wheelchair to interact with the RGS system. * Minimal experience with smartphone technology based on the clinician's opinion * Willing to participate and agree to comply with the trial scheme and procedures * Must sign an Informed Consent Form (ICF) indicating that they understand the purpose and the procedures of the study. Exclusion Criteria: * Presence of a condition or abnormality that, in the opinion of the investigator, would compromise the safety of the patient or the quality of the data. * Severe cognitive capabilities that prevent the execution of the study, evaluated by the MoCA \< 19 or based on the clinician's opinion. * Pre-stroke history of upper limb motor disability. * Unable to use the RGS independently, according to the clinician's observations, and needing more support from a caregiver to use the RGS.

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Conditions

The condition(s) this trial relates to.

stroke disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Chronic stroke patients Post stroke recovery Stroke Stroke rehabilitation

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The study's own enquiry address

    This study publishes an address for enquiries. See it below .

  2. The places running it

    2 sites in 2 countries. The list below names each one and where it is.

  3. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  4. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Study contacts

  • Contact

    Email: •••••@•••••

Locations

  • Hospital Universitari Joan XXIII de Tarragona

    RECRUITING

    Tarragona, 43005, Spain

  • RoNeuro Institute for Neurological Research and Diagnostics

    RECRUITING

    Cluj-Napoca, 400354, Romania

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