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Virtual reality offers new hope for shoulder pain sufferers

NCT ID NCT06795464

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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 adding immersive virtual reality (IVR) to standard physiotherapy helps people with long-term shoulder pain more than standard care alone. Researchers enrolled 44 adults aged 18 to 70 with rotator cuff-related shoulder pain lasting at least six months. They measured pain, shoulder function, strength, mobility, and blood biomarkers to see if IVR provides extra benefits.

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

44 people

The number who actually took part.

Started

Mar 2025

Finished

Apr 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 70 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: * Age between 18 and 70 years. * Shoulder pain persisting for at least six months. * Presence of shoulder pain during movement. * Clinical diagnosis of rotator cuff-related shoulder pain. * Willingness to participate in the study and signing of informed consent. Exclusion Criteria * Shoulder pain related to cervical spine conditions. * Presence of pain in the elbow, wrist, and/or hand. * Clinical diagnosis of frozen shoulder. * Clinical diagnosis of shoulder instability. * Cognitive impairments. * Concomitant physiotherapy treatments during the study period. * History of trauma associated with the onset of shoulder pain. * Previous fractures in the affected shoulder. * Prior surgeries in the affected shoulder. * Use of analgesic or anti-inflammatory medications within 24 hours prior to study participation. Presence of rheumatic or neurological diseases.

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Conditions

The condition(s) this trial relates to.

Chronic Pain Motor Activity Shoulder Pain

As listed by the trial registrant

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

Contacts and locations

Locations

  • Universidad Francisco de Vitoria

    Madrid, Madrid, 28223, Spain

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