Effects of Terminal Visual Feedback Therapy After Immersive Virtual Reality in Patients With Chronic Shoulder Pain
Unknown statusNot applicableNCT05640661
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The goal of this clinical trial is effect of terminal visual feedback therapy following the use of immersive virtual reality(VRi) effects on pain,kinesiophobia, fear of pain, disability, self-efficacy, grip strength and range of motion in motion in people with chronic shoulder pain compare with just VRi. The main question\[s\] it aims to answer are: * Can terminal visual feedback therapy following the use of immersive virtual reality software decrease movement-evoked pain in patients with chronic shoulder pain compared with just VRi? * Can terminal visual feedback therapy following the use of immersive virtual reality software increase shoulder flexion range of motion in patients with chronic shoulder pain compared with just VRi? Participants will use a visual feedback therapy following the use of immersive virtual reality software compared with just specific VRi software
Study details
- Official title
- Effects of Terminal Visual Feedback Therapy After Immersive Virtual Reality in Patients With Chronic Shoulder Pain : Mixed-Methods Randomized Clinical Trial
- Conditions
- Shoulder Pain
- Movement Disorders
- Interventions
- Device: Oculus Quest II
- Device: Oculus Quest II
- Sponsor
- University of Malaga
- Start date
- 2023-12-04
- Primary completion
- 2024-07-03
- Sex
- All
- Age range
- from 18 Years to 65 Years
- Results posted
- No results posted in this snapshot
- Countries
- Spain
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * People from 18 to 65 years old * Shoulder pain of at least three months of evolution located in the proximal anterolateral region of the shoulder * Presenting shoulder pain during movements with a history of traumatic or insidious onset * Agree to participate in the study and sign the informed consent Exclusion Criteria: * Shoulder pain resulting from a dysfunction of the cervical spine. * Cognitive deficits * Uso of medicines for pain control in the previous 24 hours, * A history of neurological or psychiatric disorders * Adhesive capsulitis syndrome (limited passive range of motion of the shoulder: external rotation \< 30°; elevation \< 150°) * Patients with shoulder instability * Previous surgery of the shoulder * Rheumatic diseases
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05640661