Virtual reality rehabilitation for chronic tendinopathy
Efficacy of a Physical Rehabilitation Program Using Virtual Reality in Patients With Chronic Tendinopathy (Virtendon-Rehab)
This study is testing a virtual reality rehab program to see if it helps people with chronic tendinopathy recover better and feel less pain.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 120 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Cadiz Academic / other |
| Locations | 1 site (Cadiz) |
| Trial ID | NCT06056440 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of a virtual reality-based physical rehabilitation program for patients suffering from chronic tendinopathy. The program aims to enhance recovery through engaging and competitive activities that motivate patients and allow for personalized exercise regimens. Participants will be randomly assigned to either the VR intervention group or a control group, with outcomes measured in terms of pain, functionality, range of motion, and overall quality of life. The study also seeks to characterize the clinical profiles of participants and monitor their progress throughout the treatment.
Who should consider this trial
Good fit: Ideal candidates include individuals diagnosed with chronic tendinopathy who have experienced symptoms for more than six weeks.
Not a fit: Patients with recent surgeries, contraindicating illnesses, or those who have received corticosteroid injections or exercise therapy in the last three months may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly improve recovery outcomes and quality of life for patients with chronic tendinopathy.
How similar studies have performed: While the use of virtual reality in rehabilitation is an emerging field, similar studies have shown promising results in enhancing patient engagement and recovery outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Clinical diagnosis of tendinopathy (shoulder rotator cuff tendinopathy, epicondylitis/epicondylitis, patellar tendinopathy, achilles tendinopathy). * Duration of symptoms: greater than 6 weeks. Exclusion Criteria: * People who have any pathology that prevents them from performing physical exercise. * Persons who have undergone surgery. * Persons who have an illness that may be a contraindication to the proposed procedure. * Persons who have received exercise therapy in the last 3 months. * Persons who have received corticosteroid injections in the last 3 months.
Where this trial is running
Cadiz
- Faculty of Nursing and Physiotherapy — Cadiz, Spain (Recruiting)
Study contacts
- Study coordinator: David Lucena Anton, PhD
- Email: david.lucena@uca.es
- Phone: 956015699
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.