[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"upper-extremity-fractures\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:upper-extremity-fractures":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100629538","the-effect-of-the-cold-arm-sling-elevation-pillow-on-postoperative-anxiety-and-comfort-in-children-100629538",false,"NCT07475975","The Effect of the Cold Arm Sling Elevation Pillow on Postoperative Anxiety and Comfort in Children","The Effect of Cold and Arm Sling Elevation Pillow on Postoperative Anxiety and Comfort in Pediatric Upper Extremity Fractures","Inclusion Criteria:\n\n* Children aged 7-12 years\n* Scheduled for elective surgery with a diagnosis of upper extremity fracture\n* Planned to receive analgesic treatment every 8 hours (three times daily) for postoperative pain management\n* Fully oriented and without any condition that would impair communication or cooperation\n* Expected to have a hospital stay of at least 24 hours in the orthopedic wards where the study is conducted\n* Children and their parents\u002Flegal guardians who provide consent to participate in the study\n\nExclusion Criteria:\n\n* Undergoing emergency surgical intervention\n* Presence of an open wound, infection, suspected compartment syndrome, or vascular injury at the fracture site\n* Presence of sensory loss or neurological deficit in the affected extremity\n* Presence of cognitive, hearing, speech, or severe physical disabilities\n* Treated conservatively with cast immobilization\n* Planned postoperative analgesic regimens that are more frequent or less frequent than every 8 hours, or that require high-dose analgesic therapy\n* Requiring revision surgery\n* Presence of metabolic or neuromuscular comorbidities (e.g., osteogenesis imperfecta, recurrent fractures)\n* Children whose mothers are unable to communicate or do not speak Turkish","ALL","7 Years","12 Years",{"count":20,"type":21},80,"ESTIMATED","INTERVENTIONAL",[24],"NA","The purpose of this clinical trial is to learn whether the use of a \"cold and arm sling elevation pillow\" affects anxiety and comfort levels in children aged 7-12 years undergoing surgery for upper extremity fractures. The main questions it aims to answer are:\n\n* Does the use of a cold and arm sling elevation pillow reduce postoperative anxiety levels in children?\n* Does the use of a cold and arm sling elevation pillow increase postoperative comfort levels in children?\n\nResearchers will compare the experimental group (using the specially designed cold and arm sling elevation pillow) with the control group (receiving standard clinical care, including standard pillows and separate ice packs) to see the effects of the integrated pillow on anxiety and comfort.\n\nParticipants will:\n\n* Receive education before surgery based on their randomly assigned group (experimental or control),\n* Use the assigned elevation and cold application method for the first 24 hours following surgery,\n* Complete anxiety and comfort assessment scales at four different time points: before the intervention, just before surgery, 6 hours after surgery, and at the time of discharge.",[27,28,29],"Upper Extremity Fractures","Postoperative Anxiety","Patient Comfort",[28,29,31,32,33],"Upper Extremity Fracture","Cold and arm sling elevation pillow","children","NOT_YET_RECRUITING","2026-03-23",{"date":37,"type":38},"2026-03-27","ACTUAL",{"date":40,"type":21},"2026-04-01",{"date":42,"type":21},"2027-11-01",{"name":44,"class":45},"Istanbul University - Cerrahpasa","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":66,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":46},"100597180","digital-aftercare-for-wrist-and-clavicle-fractures-100597180","NCT07055139","Digital Aftercare for Wrist and Clavicle Fractures","Comparison of Digital Versus Traditional Aftercare for Uncomplicated Distal Radius and Clavicle Fractures","DA-DRAC","Inclusion Criteria:\n\n* Age between 18 and 65 years\n* Surgically treated, uncomplicated distal radius or clavicle fracture\n* Use of a smartphone (iOS or Android)\n* Ability to understand German and complete study-related questionnaires\n* Provided written informed consent\n\nExclusion Criteria:\n\n* Polytrauma or additional injuries to the same upper extremity\n* No access to or inability to use a smartphone\n* Cognitive, psychiatric, or language barriers impairing participation\n* Pregnancy\n* Inability or unwillingness to comply with the study protocol","18 Years","65 Years",{"count":58,"type":21},84,[24],"This prospective, two-arm, open-label clinical trial compares digital aftercare with traditional follow-up in adult patients after surgical treatment of uncomplicated distal radius or clavicle fractures. The primary objective is to assess functional recovery at three months, using the Patient-Rated Wrist Evaluation (PRWE) for wrist fractures and the QuickDASH for clavicle fractures. Secondary outcomes include range of motion, patient satisfaction, quality of life, complication rates, healthcare costs, and work disability. In the digital aftercare group, program adherence and user experience will also be evaluated through app usage data and a structured questionnaire. The study aims to determine whether digital aftercare is a clinically and economically equivalent alternative to standard in-person care.",[62,63,64,65,27],"Distal Radius Fracture","Clavicle Fracture","Postoperative Care","Patient-Reported Outcome Measures (PROMs)",[67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,64],"distal radius fracture","clavicle fracture","digital aftercare","app-based aftercare","App-Based Rehabilitation","Wrist Fracture","Fracture Recovery","Functional Outcome","QuickDASH","PRWE","eHealth","Patient Satisfaction","Quality of Life","EQ-5D","Complication Rate","2025-06-27",{"date":84,"type":38},"2025-07-08",{"date":86,"type":21},"2025-09-01",{"date":88,"type":21},"2027-03-31",{"name":90,"class":45},"Luzerner Kantonsspital"]