Virtual Reality for Shoulder Rehabilitation
Goal: The clinical investigation involves the evaluation of the usability level of the VR system, sense of presence, and co-presence during the execution of various rehabilitation exercises through specific questionnaires. Participant Population: The study will enroll 50 patients with shoulder musculoskeletal disorders
| Condition(s) | Shoulder Musculoskeletal Disorders |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | Goal: The clinical investigation involves the evaluation of the usability level of the VR system, sense of presence, and co-presence during the execution of various rehabilitation exercises through specific questionnaires. Participant Population: The study will enroll 50 patients with shoulder musculoskeletal disorders will be enrolled Main Questions: * How does the integration of Virtual Reality (VR) in rehabilitation programs impact the usability of the system for patients with shoulder musculoskeletal disorders? * To what extent does the sense of presence experienced by patients using VR systems influence their motivation and adherence to rehabilitation exercises? * How do patients with shoulder musculoskeletal disorders perceive the co-presence in VR rehabilitation scenarios, and how d |
| Who can participate | Inclusion Criteria: * Patients with shoulder musculoskeletal disorders * Patients aged 18-75 years * Patients who have signed informed consent Exclusion Criteria: * Patients with insufficient cognitive and language functions to follow instructions provided by clinicians and/or experimenters involved in the project * Patients who do exhibit impediments that could hinder the use of VR devices |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Accepts healthy volunteers | Yes |
| Lead sponsor | Fondazione Policlinico Universitario Campus Bio-Medico |
| Locations | Roma, Italy, Italy; Rome, Italy, Italy |
| Start date | 2025-09-01 |
| NCT ID | NCT06797492 |
| Official listing | https://clinicaltrials.gov/study/NCT06797492 |