VR goggles could revolutionize physio for chronic shoulder pain

NCT ID NCT07392762

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 whether using virtual reality (VR) headsets during shoulder exercises is practical and acceptable for people with long-term shoulder pain. Twenty participants will do three weekly VR exercise sessions at a hospital. Researchers will measure pain, movement, and quality of life, and interview participants about their experience. The goal is to see if a larger trial is worth doing.

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 exercise program (SyncVR platform)
What this could lead to
If this approach works, it could make physiotherapy more engaging and help people stick with their exercises, potentially improving shoulder pain and function.
What could go wrong
This is a very small feasibility study with only 20 people and no control group. It is designed to see if a larger trial is possible, not to prove effectiveness. The VR program may not be suitable for everyone.

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 20 people

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

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Dec 2026

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

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: * Adult patients \>18 years with diagnosed unilateral/ bilateral shoulder pain with/ without co-existing symptoms of instability and or stiffness (persisting \> three months) generated from a Musculoskeletal origin * Patients who have been referred for conservative management * New or follow-up patients * Sufficient English to understand written materials/verbal instruction/or accompanied by family/friends able to translate * Patients who provide informed, written consent to enter the study Exclusion Criteria: * Unable to provide informed consent * On a waiting list for surgery and/or injections * Referred for post-operative physiotherapy * Shoulder pain not originating from an MSK aetiology (such as hemiplegia or peripheral nerve injury) * Active history of seizures * Other relevant medical conditions deemed inappropriate for patients to participate e.g. visual impairment, unstable psychiatric illnesses. * Shoulder pain associated with bone metastasis * Currently taking part in any other upper limb research study * Patients who do not adequately understand verbal explanations or written information given in English (or are not accompanied by an interpreter/family member).

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Conditions

The condition(s) this trial relates to.

Shoulder Pain

As listed by the trial registrant

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

How to take part

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

  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

  • Royal National Orthopaedic Hospital

    Middlesex, London, HA74LP, United Kingdom

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