[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cubital-tunnel-syndrome\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cubital-tunnel-syndrome":42},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,63,86,119],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":44,"overallStatus":50,"whyStopped":4,"lastUpdateSubmitDate":51,"lastUpdatePostDateStruct":52,"startDateStruct":55,"completionDateStruct":57,"leadSponsor":59,"locationsCount":62},"100633082","early-functional-response-as-a-predictor-of-clinical-outcomes-in-hand-rehabilitation-a-prospective-feasibility-study-using-a-digital-monitoring-system-100633082",false,"NCT07522060","Early Functional Response as a Predictor of Clinical Outcomes in Hand Rehabilitation: A Prospective Feasibility Study Using a Digital Monitoring System","Early Functional Response as a Predictor of Clinical Outcomes in Hand Rehabilitation: A Prospective Feasibility Study Using a Clinician-Developed Digital Monitoring System","HANDREHPREDICT","Inclusion Criteria:\n\n* Adults aged 18 years or older\n* Hand or upper extremity pathology requiring rehabilitation, including but not limited to: flexor or extensor tendon injuries, peripheral nerve injuries or compression syndromes (including carpal tunnel syndrome, cubital tunnel syndrome), distal radius fractures, metacarpal or phalangeal fractures, joint injuries and instabilities, arthropathy (osteoarthritis, rheumatoid arthritis), trapeziometacarpal osteoarthritis, trigger finger, Dupuytren's disease, DeQuervain tenosynovitis, lateral epicondylitis and post-surgical upper extremity conditions\n* Under clinical responsibility of the principal investigator at the Faculty of Physical Therapy and Rehabilitation, Hacettepe University\n* Expected to attend minimum 8 rehabilitation sessions\n* Able to provide written informed consent\n\nExclusion Criteria:\n\n* • Active psychiatric illness precluding participation or completion of assessment tools\n\n  * Severe cognitive impairment precluding understanding of patient-reported outcome measures\n  * Literacy difficulties preventing self-completion of questionnaires\n  * Concurrent enrollment in another interventional clinical study\n  * Refusal to provide written informed consent","ALL","18 Years",{"count":20,"type":21},60,"ESTIMATED","OBSERVATIONAL","This study investigates whether early changes observed during the first weeks of hand and upper extremity rehabilitation can predict patient outcomes months later. In rehabilitation practice, clinicians make numerous decisions each session regarding exercise type, frequency, duration, and treatment approach. Most of these decisions are currently made without systematic longitudinal data. This study addresses three fundamental questions using data collected during routine clinical care: (1) Can the rate of improvement in the first weeks of treatment predict functional status months later, across both session-based and milestone-based time points? (2) Are there meaningfully different recovery profiles among hand rehabilitation patients? (3) Is there measurable variation in clinical decision-making among patients with similar profiles, and does this variation relate to outcomes? A digital patient monitoring platform developed by the principal investigator, a physiotherapist and academic researcher specializing in hand rehabilitation serves as the data collection infrastructure. The platform records standard clinical assessment measures in a structured format and has been in active clinical use at Hacettepe University prior to this study. For research purposes, the system has been expanded to include structured capture of patient-reported outcomes, patient global impression of change, treatment protocol coding, home exercise adherence, and automated calculation of early response metrics.\n\nThis is a 12-month prospective observational cohort study enrolling a minimum of 60 patients. Data are stored securely on the university's institutional network. Patients are anonymized using identification codes. The study is subject to Hacettepe University Ethics Committee approval and participant informed consent. Findings are expected to generate evidence supporting data-driven clinical decision-making in rehabilitation and to provide a feasibility foundation for a larger multi-center study.",[25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43],"Hand","Hand Therapy","Upper Extremity","Prediction Models","Hand Injuries","Hand Injuries and Disorders","Hand Arthritis","Tendon Injuries","Wrist Fractures","Carpal Tunnel Syndrome (CTS)","Peripheral Nerve Injuries","Upper Extremity Injuries","Wrist Injuries","Finger Injuries","Trigger Finger","Trapeziometacarpal (TMC) Arthrosis","DeQuervain's Tenosynovitis","Cubital Tunnel Syndrome","Postoperative Rehabilitation",[45,46,47,48,49],"digital health monitoring","real-world evidence","clinical decision support","upper extremity rehabilitation","early response prediction","NOT_YET_RECRUITING","2026-04-03",{"date":53,"type":54},"2026-04-13","ACTUAL",{"date":56,"type":21},"2026-06-15",{"date":58,"type":21},"2027-06-01",{"name":60,"class":61},"Hacettepe University","OTHER",1,{"id":64,"slug":65,"hasResults":11,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":4,"eligibilityCriteria":69,"healthyVolunteers":70,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":71,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":73,"conditions":74,"keywords":4,"overallStatus":76,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":62},"100631109","median-and-ulnar-nerve-function-in-tattoo-artists-100631109","NCT07496398","Median and Ulnar Nerve Function in Tattoo Artists","Occupational Hand-Arm Vibration Exposure and Its Effects on Median and Ulnar Nerve Function in Tattoo Artists: A Case-Control Study","Inclusion Criteria:\n\n* Age ≥ 18 years\n* Professional tattoo artists with at least 1 year of occupational experience (case group)\n* Healthy individuals without occupational vibration exposure (control group)\n* Voluntary participation and provision of informed consent\n* No upper extremity trauma or surgery within the last 6 months\n\nExclusion Criteria:\n\n* Diagnosis of diabetes mellitus\n* Diagnosis of peripheral neuropathy\n* History of cervical radiculopathy or cervical disc herniation\n* History of upper extremity surgery or injury\n* Presence of rheumatologic or systemic inflammatory diseases\n* Pregnancy\n* Substance or alcohol abuse\n* Engagement in a second occupation involving repetitive hand use or vibration exposure",true,{"count":72,"type":21},20,"This case-control study aims to investigate the effects of occupational hand-arm vibration exposure on median and ulnar nerve functions in tattoo artists. Chronic exposure to vibration generated by tattoo machines may lead to neurosensory impairment, reduced tactile sensitivity, and decreased hand strength. Objective assessments including nerve provocation tests, sensory threshold evaluation, two-point discrimination, vibration perception, grip and pinch strength measurements, and validated patient-reported outcome questionnaires will be used. Findings will be compared with age- and sex-matched healthy controls.",[75,34,42],"Peripheral Neuropathy Pain","RECRUITING","2026-03-23",{"date":79,"type":54},"2026-03-27",{"date":81,"type":54},"2026-03-01",{"date":83,"type":21},"2026-08-01",{"name":85,"class":61},"Gazi University",{"id":87,"slug":88,"hasResults":11,"nctId":89,"briefTitle":90,"officialTitle":91,"acronym":4,"eligibilityCriteria":92,"healthyVolunteers":70,"sex":17,"minAge":18,"maxAge":93,"enrollmentInfo":94,"targetDuration":4,"studyType":96,"phases":97,"briefSummary":99,"conditions":100,"keywords":102,"overallStatus":76,"whyStopped":4,"lastUpdateSubmitDate":110,"lastUpdatePostDateStruct":111,"startDateStruct":113,"completionDateStruct":115,"leadSponsor":117,"locationsCount":62},"100469661","conditioning-electrical-stimulation-to-improve-outcomes-in-cubital-tunnel-syndrome-100469661","NCT05395715","Conditioning Electrical Stimulation to Improve Outcomes in Cubital Tunnel Syndrome","Conditioning Electrical Stimulation Enhances Recovery Following Surgery for Severe Cubital Tunnel Syndrome: A Double-Blind Randomized Controlled Trial","Inclusion Criteria:\n\n1. Patients aged \\>18 yr,\n2. If signs and symptoms of severe CuTS (ie, McGowan-Goldberg grade 3) were observed,\n3. If needle EMG examination showed evidence of chronic motor axonal loss and reduced recruitment in the ulnar-innervated intrinsic hand muscles, and\n4. If electrophysiologic evidence of severe motor axonal loss with motor unit number estimation (MUNE) greater than 2 standard deviations below the normative mean.\n\nExclusion Criteria:\n\n1\\) Patients were excluded if they had concurrent nerve injury, prior surgery for CuTS or coexisting neurologic conditions","79 Years",{"count":95,"type":21},30,"INTERVENTIONAL",[98],"NA","Cubital tunnel syndrome is the second most common compression neuropathy. In severe cases, functional recovery, even with surgery, is often poor. Therefore, alternative adjunct treatments capable of increasing the speed of nerve regeneration are much needed.",[42,101],"Electrical Stimulation",[103,104,105,106,107,108,109],"Cubital tunnel syndrome","Nerve regeneration","Electrical stimulation","Functional outcomes","Randomized control trial","Surgery","Peripheral nerve regeneration","2026-02-04",{"date":112,"type":54},"2026-02-09",{"date":114,"type":54},"2022-04-01",{"date":116,"type":21},"2028-06-28",{"name":118,"class":61},"University of Alberta",{"id":120,"slug":121,"hasResults":11,"nctId":122,"briefTitle":123,"officialTitle":123,"acronym":4,"eligibilityCriteria":124,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":125,"enrollmentInfo":126,"targetDuration":4,"studyType":96,"phases":128,"briefSummary":129,"conditions":130,"keywords":133,"overallStatus":76,"whyStopped":4,"lastUpdateSubmitDate":136,"lastUpdatePostDateStruct":137,"startDateStruct":139,"completionDateStruct":141,"leadSponsor":143,"locationsCount":145},"100593028","investigation-of-the-effectiveness-of-kinesiological-taping-in-cubital-tunnel-syndrome-100593028","NCT07001111","Investigation of the Effectiveness of Kinesiological Taping in Cubital Tunnel Syndrome","Inclusion Criteria:\n\n* Aged between 18 and 65 years\n* Patients with at least 3 points of pain according to the Numeric Rating Scale (NRS)\n* Patients diagnosed with Cubital Tunnel Syndrome via Electroneuromyography (ENMG)\n* Literate\n* Willing to consent to participate in the study\n\nExclusion Criteria:\n\n* Having any secondary entrapment neuropathy such as diabetes, inflammatory arthritis, or hypothyroidism\n* Pregnancy\n* Active cancer presence\n* Skin infection, burns, wounds, or scars on the forearm\n* History of elbow trauma\n* Cervical radiculopathy or brachial plexopathy\n* Polyneuropathy\n* Having previously undergone Cubital Tunnel decompression surgery\n* Having received a corticosteroid injection into the Cubital Tunnel within the last 3 months\n* Illiterate\n* Not consenting to participate in the study","65 Years",{"count":127,"type":21},36,[98],"This study aims to investigate the effect of kinesiological taping, applied in addition to exercise, on clinical symptoms in patients diagnosed with Cubital Tunnel Syndrome. The patients will be randomized into three groups (exercise, exercise + kinesiological taping, exercise + sham taping) and will be evaluated at the 1st and 3rd months after a 3-week treatment period.",[42,131,132],"Kinesio Taping","Ulnar Neuropathies",[42,134,135],"Kinesio taping","ulnar neuropathies","2025-09-05",{"date":138,"type":54},"2025-09-12",{"date":140,"type":54},"2025-04-21",{"date":142,"type":21},"2026-02",{"name":144,"class":61},"Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey",2]