[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100577376":3},{"organization":4,"armGroups":7,"interventions":16,"overallOfficials":22,"centralContacts":32,"locations":38,"responsibleParty":63,"collaborators":22,"id":67,"slug":68,"hasResults":69,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":73,"eligibilityCriteria":74,"healthyVolunteers":75,"sex":76,"minAge":77,"maxAge":78,"enrollmentInfo":79,"targetDuration":22,"studyType":82,"phases":83,"briefSummary":85,"conditions":86,"keywords":88,"overallStatus":40,"whyStopped":22,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":101},{"fullName":5,"class":6},"Fondazione Policlinico Universitario Campus Bio-Medico","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Patients with shoulder musculoskeletal disorders","EXPERIMENTAL","The study will involve 50 adults with shoulder musculoskeletal disorders. Eligible participants are those over 18 with significant shoulder pathologies, excluding individuals with neurological conditions, infections, inflammatory diseases, major previous shoulder surgeries, or pregnancy. After obtaining informed consent, baseline demographic and anthropometric data will be collected. Patients will be assessed by a clinician across four rehabilitation phases: T1 (0-4\u002F6 weeks), T2 (6-12 weeks), T3 (12-20 weeks), and T4 (beyond 20 weeks). Each phase includes a shoulder examination followed by a 30-minute VR-based rehabilitation session, customized to the patient's physical characteristics.",[13,14,15],"Diagnostic Test: Shoulder Physical Examination","Procedure: Shoulder Rehabilitation in a Virtual Environment","Other: Usability assessment and presence and co-presence evaluation",[17,23,28],{"type":18,"name":19,"description":20,"armGroupLabels":21,"otherNames":22},"DIAGNOSTIC_TEST","Shoulder Physical Examination","shoulder physical examination is conducted to assess the patient's musculoskeletal condition and to track progress throughout the rehabilitation phases",[9],null,{"type":24,"name":25,"description":26,"armGroupLabels":27,"otherNames":22},"PROCEDURE","Shoulder Rehabilitation in a Virtual Environment","The rehabilitation protocol for shoulder disorders is executed using a Virtual Reality (VR) system, where patients perform customized exercises tailored to their physical characteristics.",[9],{"type":6,"name":29,"description":30,"armGroupLabels":31,"otherNames":22},"Usability assessment and presence and co-presence evaluation","The usability of the VR system, along with the sense of presence and co-presence during rehabilitation, is assessed using validated scales",[9],[33],{"name":34,"role":35,"phone":36,"phoneExt":22,"email":37},"Umile Giuseppe Longo, MD, MSc, PhD","CONTACT",": +39 06225418816","g.longo@policlinicocampus.it",[39,55],{"facility":5,"status":40,"city":41,"state":42,"zip":43,"country":42,"countryCode":44,"cosmosGeoPoint":45,"geoPoint":50,"contacts":51},"RECRUITING","Roma","Italy","00128","IT",{"type":46,"coordinates":47},"Point",[48,49],11.10642,44.99364,{"lat":49,"lon":48},[52],{"name":53,"role":35,"phone":54,"phoneExt":22,"email":37},"Umile Giuseppe Longo, PhD","06225411",{"facility":5,"status":56,"city":57,"state":42,"zip":43,"country":42,"countryCode":44,"cosmosGeoPoint":58,"geoPoint":62,"contacts":22},"NOT_YET_RECRUITING","Rome",{"type":46,"coordinates":59},[60,61],12.51133,41.89193,{"lat":61,"lon":60},{"type":64,"investigatorFullName":65,"investigatorTitle":66,"investigatorAffiliation":5,"oldNameTitle":22,"oldOrganization":22},"PRINCIPAL_INVESTIGATOR","Umile Giuseppe Longo","Professor","100577376","virtual-reality-for-shoulder-rehabilitation-100577376",false,"NCT06797492","Virtual Reality for Shoulder Rehabilitation","Virtual Reality for Shoulder Rehabilitation: New Approaches and Applications in Orthopedics","REVISA","Inclusion Criteria:\n\n* Patients with shoulder musculoskeletal disorders\n* Patients aged 18-75 years\n* Patients who have signed informed consent\n\nExclusion Criteria:\n\n* Patients with insufficient cognitive and language functions to follow instructions provided by clinicians and\u002For experimenters involved in the project\n* Patients who do exhibit impediments that could hinder the use of VR devices",true,"ALL","18 Years","75 Years",{"count":80,"type":81},50,"ESTIMATED","INTERVENTIONAL",[84],"NA","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.\n\nParticipant Population: The study will enroll 50 patients with shoulder musculoskeletal disorders will be enrolled\n\nMain Questions:\n\n* How does the integration of Virtual Reality (VR) in rehabilitation programs impact the usability of the system for patients with shoulder musculoskeletal disorders?\n* To what extent does the sense of presence experienced by patients using VR systems influence their motivation and adherence to rehabilitation exercises?\n* How do patients with shoulder musculoskeletal disorders perceive the co-presence in VR rehabilitation scenarios, and how does it affect their overall treatment experience?\n\nParticipant Tasks:\n\n* Shoulder Physical Examination\n* Instructions to the patient on exercises to be performed using Oculus and selection of customizable settings on the VR app\n* Execution of the protocol developed for shoulder rehabilitation in a virtual environment\n* Evaluation of the usability of the VR system, sense of presence, and co-presence through different validated scales",[87],"Shoulder Musculoskeletal Disorders",[89,90,91],"Musculoskeletal disorders","shoulder rehabilitation","virtual reality","2026-03-02",{"date":94,"type":95},"2026-03-04","ACTUAL",{"date":97,"type":95},"2025-09-01",{"date":99,"type":81},"2027-12",{"name":5,"class":6},2]