[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hand-arthritis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hand-arthritis":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,45,91],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100579148","trapeziectomy-and-suture-suspensionplasty-for-thumb-carpometacarpal-arthritis---is-in-clinic-therapy-needed-100579148",false,"NCT06820528","Trapeziectomy and Suture Suspensionplasty for Thumb Carpometacarpal Arthritis - Is In-Clinic Therapy Needed?","Inclusion Criteria:\n\n* Patients over the age of 18 years\n* Patients undergoing CMC Arthroplasty\n* Ability to read and write in English\n* Ability to provide informed consent\n\nExclusion Criteria:\n\n* Patients undergoing revision CMC arthroplasty\n* Acute traumatic dislocation of the CMC joint as indication for surgery\n* Concomitant treatment of MCP hyperextension","ALL","18 Years",{"count":18,"type":19},180,"ESTIMATED","INTERVENTIONAL",[22],"NA","The study is a randomized, controlled trial to evaluate the efficacy of formal occupational therapy on outcomes following CMC arthroplasty",[25,26,27],"CMC Arthritis","Occupational Therapy","Hand Arthritis",[29,30,31],"CMC Arthroplasty","Thumb Arthritis","Hand Therapy","RECRUITING","2026-06-03",{"date":35,"type":36},"2026-06-05","ACTUAL",{"date":38,"type":36},"2025-04-17",{"date":40,"type":19},"2028-01-01",{"name":42,"class":43},"Julie Nuelle","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":55,"phases":4,"briefSummary":56,"conditions":57,"keywords":75,"overallStatus":81,"whyStopped":4,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":44},"100633082","early-functional-response-as-a-predictor-of-clinical-outcomes-in-hand-rehabilitation-a-prospective-feasibility-study-using-a-digital-monitoring-system-100633082","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",{"count":54,"type":19},60,"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.",[58,31,59,60,61,62,27,63,64,65,66,67,68,69,70,71,72,73,74],"Hand","Upper Extremity","Prediction Models","Hand Injuries","Hand Injuries and Disorders","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",[76,77,78,79,80],"digital health monitoring","real-world evidence","clinical decision support","upper extremity rehabilitation","early response prediction","NOT_YET_RECRUITING","2026-04-03",{"date":84,"type":36},"2026-04-13",{"date":86,"type":19},"2026-06-15",{"date":88,"type":19},"2027-06-01",{"name":90,"class":43},"Hacettepe University",{"id":92,"slug":93,"hasResults":11,"nctId":94,"briefTitle":95,"officialTitle":96,"acronym":4,"eligibilityCriteria":97,"healthyVolunteers":11,"sex":15,"minAge":98,"maxAge":4,"enrollmentInfo":99,"targetDuration":4,"studyType":20,"phases":100,"briefSummary":101,"conditions":102,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":44},"100586262","ultrasonication-mediated-microbubbles-dressing-for-hand-arthritis-100586262","NCT06913088","Ultrasonication-mediated Microbubbles Dressing for Hand Arthritis","Ultrasonication-mediated Microbubbles Dressings Increase the Therapeutic Efficacy of Piroxicam Gel for Hand Arthritis: Assessments Using Conventional and Ultrafast Power Doppler Imaging","Inclusion Criteria:\n\n* Clinical diagnosis of hand arthritis\n* Have at least three symptomatic joints over wrist, metacarpophalangeal joints, and interphalangeal joints\n\nExclusion Criteria:\n\n* Infectious arthritis\n* Acute gout","20 Years",{"count":54,"type":19},[22],"The goal of this clinical trial is to learn if ultrasonication-mediated microbubbles dressing works to treat hand arthritis in adults. It will also learn about the safety of ultrasonication-mediated microbubbles dressing. The main questions it aims to answer are:\n\nDoes ultrasonication-mediated microbubbles dressing increase the therapeutic efficacy of piroxicam gel for hand arthritis?\n\nResearchers will compare \"ultrasonication-mediated microbubbles dressing + piroxicam gel \" to \"ultrasonication + piroxicam gel\" and \"piroxicam gel alone\" to see if ultrasonication-mediated microbubbles dressing works to treat hand arthritis.\n\nParticipants will:\n\nTake \"ultrasonication-mediated microbubbles dressing (day 1,3,5) + piroxicam gel (day 2,4,6,7) \", \"ultrasonication (day 1,3,5) + piroxicam gel (day 2.4.6.7)\", and \"piroxicam gel alone (day 1-7)\" for 1 week.\n\nVisit the clinic on day 1 and day 8 for checkups and tests Keep a diary of their symptoms",[27],"2025-04-14",{"date":38,"type":36},{"date":106,"type":36},"2025-04-02",{"date":108,"type":19},"2026-03-31",{"name":110,"class":43},"National Taiwan University"]