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Can virtual reality help seniors move better? new trial investigates

NCT ID NCT07026890

Symptom relief Sponsor: Centre Hospitalier Universitaire Dijon 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether virtual reality (VR) can improve movement in elderly people with Psychomotor Disadaptation Syndrome, a condition that affects balance and walking. Fifty hospitalized patients will either receive standard rehab or VR sessions three times a week. The goal is to see if VR makes rehab more effective and engaging.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
virtual reality rehabilitation sessions
What this could lead to
If it works, this could offer a more engaging and effective way to help elderly patients regain mobility and reduce fall risk.
What could go wrong
This is a small, early-stage trial with only 50 participants, so results may not apply widely. VR may not be better than standard exercises and could cause discomfort or dizziness in some patients.

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 50 people

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

Started

Jul 2025

Expected to finish

Sep 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

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

Ages

65 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: * Person who has given written consent * Person aged ≥ 65 years; * With a proven diagnosis of motor maladjustment syndrome; * Hospitalised in a geriatric care unit; * Able to understand a simple instruction and answer a closed question; * Ability to perform the TUG within 7 days of arriving on site Exclusion Criteria: * Person not affiliated to or not benefiting from a social security scheme * Person subject to a legal protection measure (curatorship, guardianship) * Person subject to a judicial protection measure * An adult who is incapable or unable to give consent * Persons with epilepsy, kinetosis or known claustrophobia Persons unable to understand simple instructions for carrying out tests * Anyone with a severe visual and/or hearing impairment * Any person with a behavioural disorder (agitation, aggressiveness) * Any person with a severe walking or balance problem that makes motor exercises unsuitable * Anyone with a pathology, injury, wound or severe deformity to the head or cervical spine * Any person suffering from severe vertigo, diagnosed at the discretion of the investigating doctor * Inability to use arm for pointing * Persons susceptible to migraines * Non-French speakers * Anyone with an inter-pupillary distance outside the range of possible helmet adjustments

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As listed by the trial registrant

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

Psychomotor disadaptation syndrome

How to take part

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. 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 ↗

  3. 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

Locations

  • CHU Dijon Bourgogne

    RECRUITING

    Dijon, 21000, France

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