Using virtual reality to help rehabilitate shoulder injuries
Official title: Personalized Rehabilitation System Using Gamification With Virtual Reality Technology: A Feasibility Study
Run by La Tour Hospital · NCT06963983 · Data updated 2026-11-12
This study tests whether using virtual reality can make shoulder rehabilitation more engaging and effective for people with shoulder injuries.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 15 (estimated) |
| Sponsor | La Tour Hospital Academic / other |
| Locations | 1 site (Meyrin, Canton of Geneva) |
| Status | Recruiting |
| Started | October 28, 2024 |
| Main results expected | June 28, 2025 |
| Study ends | June 28, 2025 |
| Registry record updated | May 9, 2025 |
| Trial ID | NCT06963983 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults with specific shoulder conditions such as glenohumeral instability, rotator cuff repairs, or frozen shoulder who are able to understand and consent to the study.
✕Probably not a fit
Patients with language barriers, those unlikely to attend follow-ups, or individuals with legal incompetence may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study explores the use of virtual reality (VR) technology to enhance rehabilitation for patients with shoulder pathologies such as instability, frozen shoulder, and rotator cuff tears. By integrating modern motion-tracking with VR, the study aims to improve patient engagement and compliance during rehabilitation exercises, which are often repetitive and can lead to decreased motivation. The goal is to determine if this innovative approach can lead to better functional outcomes compared to traditional rehabilitation methods.
Why it matters
Potential benefit: If successful, this approach could significantly improve recovery outcomes and patient satisfaction in shoulder rehabilitation.
How similar studies have gone: Previous studies have shown benefits of VR in rehabilitation, particularly in post-stroke recovery, but this specific application for shoulder pathologies is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patients able to understand the content of the patient information / consent form and give consent to take part in the research project * Glenohumeral instability surgical treated with traumatic initial instability in a \< 20 years old athlete, recurrent instability with one or more of the following criteria: a failure of conservative treatment, locked dislocation, failed prior surgery, high risk for further recurrence (i.e. collision or competitive athletes), Critical glenoid bone-loss (\>15-20%), bipolar bone-loss resulting in "off-track" lesion * Partial or complete rotator cuff repair with an indication to postoperative rehabilitation depending on surgeon recommendation * Idiopathic, primary, or secondary frozen shoulder Exclusion Criteria: * Patients with a language barrier hindering questionnaires completion * Patients unlikely to attend clinical follow-up (e.g. when living abroad) * Legal incompetence * Enrolment of the investigators, his/her family members, employees and other dependent persons * Non-motivated patients * Active infection * Exclusion criteria related to glenohumeral instability: uncontrolled epilepsy, spontaneous unidirectional instability in a hyperlax patient, multidirectional instability, elher-Danlos syndrome * Exclusion criteria related to rotator cuff tears: Additional procedure(s) (muscle transfer, patch,…) * Exclusion criteria related to VR use: Patients with a predisposition to motion sickness, Patients suffering from epilepsy or having any serious mental illness (schyzophrenia, neurological problems, etc.), Patients with visual impairment , Patients will intellectual disability that prevent them to understand how to use the VR rehabilitation system, Patients with bilateral upper limb injuries, as one side is needed as healthy reference
Where it's running
-
La Tour hospital
Meyrin, Canton of Geneva, Switzerland Recruiting
Study contacts
- Principal investigator: Alexandre Lädermann, MD — La Tour hospital, Meyrin (1217) Geneva, Switzerland
- Study coordinator: Alexandre Lädermann, MD
- Email: alexandre.laedermann@gmail.com
- Phone: +41 22 719 75 55
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Dynamic Anterior Stabilization vs Bankart Repair for recurrent shoulder instability
This study tests whether Dynamic Anterior Stabilization (DAS) or traditional Bankart repair better stabilizes the shoulder in people under 50 with recurring anterior instability and 10-20% glenoid bone loss.
-
Rotator cuff repair with biceps rerouting and dermal graft augmentation for large, difficult tears
This study tests a combined surgical approach to see if it helps tendon retear rates in adults with large rotator cuff tears that are hard to repair.
-
Biomarkers to see if rotator cuff repairs will heal after surgery
This study tests whether biomarkers in shoulder tissue and synovial fluid can predict whether a rotator cuff repair will heal, using MRI after surgery to compare those who heal with those who don’t.
-
Spinal and Kaltenborn mobilization for a stiff shoulder (frozen shoulder)
A randomized trial tests spinal mobilization with arm movement and Kaltenborn mobilization to see if they reduce pain and improve motion and function in people with adhesive capsulitis.
-
Shoulder Frozen Shoulder: TAME vs Corticosteroid Injection
This study tests whether transcatheter arterial microembolization (TAME) works better than corticosteroid injections for people with frozen shoulder.
-
Modified PENG plus SSNB vs Interscalene block for Bankart and Latarjet surgery
This trial tests whether a Modified PENG block with a Suprascapular Nerve Block provides similar pain relief to an Interscalene block for adults having Bankart repair or Latarjet surgery.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.