[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100644233":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":10,"centralContacts":24,"locations":10,"responsibleParty":30,"collaborators":10,"id":34,"slug":35,"hasResults":36,"nctId":37,"briefTitle":38,"officialTitle":38,"acronym":10,"eligibilityCriteria":39,"healthyVolunteers":36,"sex":40,"minAge":41,"maxAge":42,"enrollmentInfo":43,"targetDuration":10,"studyType":46,"phases":10,"briefSummary":47,"conditions":48,"keywords":10,"overallStatus":50,"whyStopped":10,"lastUpdateSubmitDate":51,"lastUpdatePostDateStruct":52,"startDateStruct":55,"completionDateStruct":57,"leadSponsor":59,"locationsCount":10},{"fullName":5,"class":6},"Kanuni Sultan Suleyman Training and Research Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Patients with Central Sensitization",null,"Patients with supraspinatus partial-thickness tears who are classified as having central sensitization based on the Central Sensitization Inventory (CSI) at baseline and who receive the standardized physical therapy program.",[13],"Behavioral: Standard Physical Therapy and Rehabilitation",{"label":15,"type":10,"description":16,"interventionNames":17},"Patients without Central Sensitization","Patients with supraspinatus partial-thickness tears who are classified as not having central sensitization based on the Central Sensitization Inventory (CSI) at baseline and who receive the same standardized physical therapy program.",[13],[19],{"type":20,"name":21,"description":22,"armGroupLabels":23,"otherNames":10},"BEHAVIORAL","Standard Physical Therapy and Rehabilitation","All participants will receive the same standardized physical therapy and rehabilitation program administered according to routine clinical practice. The treatment program will include therapeutic exercises, stretching, strengthening, range-of-motion exercises, and appropriate physical therapy modalities as determined by the rehabilitation protocol. No experimental intervention or additional procedure will be performed for research purposes. The study is observational and aims to evaluate whether the presence of central sensitization influences the clinical response to the standardized rehabilitation program.",[9,15],[25],{"name":26,"role":27,"phone":28,"phoneExt":10,"email":29},"Zeynep Karakuzu Güngör, M.D","CONTACT","+90 (212) 404 15 00.","zeynepkarakuzu@hotmail.com.tr",{"type":31,"investigatorFullName":32,"investigatorTitle":33,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","Zeynep Karakuzu Güngör","Specialist Physician in Physical Medicine and Rehabilitation","100644233","effect-of-central-sensitization-on-response-to-physical-therapy-in-patients-with-partial-supraspinatus-tear-100644233",false,"NCT07664137","Effect of Central Sensitization on Response to Physical Therapy in Patients With Partial Supraspinatus Tear","Inclusion Criteria:\n\nAdults aged 18 to 65 years. Diagnosis of supraspinatus partial-thickness tear confirmed by clinical examination and magnetic resonance imaging (MRI).\n\nPresence of shoulder pain for at least 6 weeks. Candidates for a standardized physical therapy and rehabilitation program. Ability to understand the study procedures and provide written informed consent.\n\nExclusion Criteria:\n\nFull-thickness rotator cuff tear or history of previous shoulder surgery on the affected side.\n\nAcute fracture, shoulder dislocation, or other major traumatic injury involving the affected shoulder.\n\nInflammatory rheumatic diseases, active infection, or malignancy affecting the musculoskeletal system.\n\nNeurological disorders that may influence pain perception or upper extremity function (e.g., stroke, cervical myelopathy, peripheral neuropathy).\n\nSevere glenohumeral or acromioclavicular osteoarthritis requiring surgical treatment.\n\nReceipt of corticosteroid injection or any invasive shoulder intervention within the previous 3 months.\n\nParticipation in another structured rehabilitation program for the affected shoulder within the previous 3 months.\n\nPregnancy or inability to comply with the study protocol or complete the required questionnaires.","ALL","18 Years","65 Years",{"count":44,"type":45},60,"ESTIMATED","OBSERVATIONAL","This prospective observational study aims to investigate whether central sensitization influences the response to physical therapy in patients with partial supraspinatus tendon tears. Participants will undergo standardized clinical evaluation before treatment and after a 6-week physical therapy program. Pain intensity, shoulder function, disability, and central sensitization-related symptoms will be assessed using validated outcome measures. The study seeks to determine the relationship between baseline central sensitization status and treatment outcomes, thereby identifying factors that may predict rehabilitation success and support individualized treatment strategies for patients with partial supraspinatus tears.",[49],"Rotator Cuff Tears","NOT_YET_RECRUITING","2026-06-17",{"date":53,"type":54},"2026-06-24","ACTUAL",{"date":56,"type":45},"2026-06-30",{"date":58,"type":45},"2026-11-30",{"name":5,"class":6}]