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Virtual reality could help quadriplegics control hand devices before surgery

NCT ID NCT07642804

Knowledge-focused Sponsor: Centre Bouffard Vercelli - USSAP Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested whether virtual reality can be used to evaluate and improve control interfaces for a neuroprosthesis that stimulates hand movements in people with complete tetraplegia (quadriplegia). Ten participants with spinal cord injuries tried two different control methods in a virtual environment to see how well they could grasp and hold objects. The goal was to find a way to customize and practice using the device before it is implanted, making future use more effective and less frustrating.

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

10 people

The number who actually took part.

Started

Apr 2026

Finished

May 2026

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

18 to 80 years

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: * Spinal cord injury defined by an AIS A, B or score (AIS A, B): complete or incomplete motor deficit below the lesion. This is a standard for describing spinalcord injuries that has been internationally agreed upon. * Spinal cord injury at the neurological level \> C7 * Age greater than or equal to 18 and less than or equal to 80 years * A history of more than 3 months of neurological stability, with no changes in muscle testing. * Participants capable of following instructions for testing and providing feedback on the use of the device. * Participants who have signed the informed consent form to participate in the study after being fully informed. * Participants affiliated with a social security system (either as a beneficiary or a dependent), excluding those covered by State Medical Aid (AME). Exclusion Criteria: * • Participant deprived of liberty (by judicial or administrative decision). * Adult participants are under legal protection or unable to provide informed consent. * Participation in another ongoing clinical trial. * Unstable psychiatric condition. * Severe cognitive impairment. * Unstable acute medical condition * Insufficient proficiency in spoken and written French.

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Conditions

The condition(s) this trial relates to.

quadriplegia

As listed by the trial registrant

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

Intervention study

Contacts and locations

Locations

  • Rehabilitation Center Bouffard-Vercelli USSAP

    Perpignan, 66000, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.