[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100635221":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":25,"centralContacts":30,"locations":25,"responsibleParty":36,"collaborators":25,"id":40,"slug":41,"hasResults":42,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":25,"eligibilityCriteria":46,"healthyVolunteers":42,"sex":47,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":25,"studyType":53,"phases":54,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":63,"whyStopped":25,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":25},{"fullName":5,"class":6},"West China Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Clinic rehabilitation group","ACTIVE_COMPARATOR","Postoperatively, patients received systematic on-site rehabilitation guidance from a therapist and were permitted to continue rehabilitation at home independently only after mastering the essential techniques of the prescribed exercises.",[13],"Other: Clinic rehabilitation",{"label":15,"type":16,"description":17,"interventionNames":18},"Telerehabilitation group","EXPERIMENTAL","Postoperatively, patients underwent systematic telerehabilitation training assisted by smart wearable devices.",[19],"Other: Telerehabilitation intervention based on wearable devices",[21,26],{"type":6,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"Telerehabilitation intervention based on wearable devices","This model integrated 5G network connectivity, mobile terminal applications, and wearable devices, enabling patients to perform rehabilitation exercises under real-time video and audio guidance. Patients underwent systematic telerehabilitation training assisted by wearable devices, following the same rehabilitation protocol as the on-site rehabilitation group. The patients installed the software on their smartphones and received a 24-week daily exercise program through the software platform. The rehabilitation training content for each phase was developed by a therapist on the software backend and then delivered to the patient via the application.",[15],null,{"type":6,"name":27,"description":28,"armGroupLabels":29,"otherNames":25},"Clinic rehabilitation","Patients in the on-site rehabilitation group attended outpatient follow-up visits at 2, 6, 12, and 24 weeks postoperatively. During these visits, they received one-on-one, face-to-face systematic exercise rehabilitation training and guidance from a uniformly trained rehabilitation therapist, with at least one session per time point, each lasting 40 minutes. After mastering the essential techniques of the prescribed exercises, patients continued rehabilitation at home independently according to the established protocol.",[9],[31],{"name":32,"role":33,"phone":34,"phoneExt":25,"email":35},"Qian Deng","CONTACT","+86 134-3807-6366","dengqianre@163.com",{"type":37,"investigatorFullName":38,"investigatorTitle":39,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"PRINCIPAL_INVESTIGATOR","Deng Qian","Rehabilitation therapist","100635221","application-of-smart-wearable-device-based-remote-rehabilitation-in-postoperative-recovery-after-arthroscopic-surgery-for-discoid-meniscus-100635221",false,"NCT07549867","Application of Smart Wearable Device-Based Remote Rehabilitation in Postoperative Recovery After Arthroscopic Surgery for Discoid Meniscus","Application of Smart Wearable Device-Based Remote Rehabilitation in Postoperative Recovery After Arthroscopic Surgery for Discoid Meniscus: A Prospective, Randomized Controlled Trial Protocol","Inclusion Criteria:\n\n* 1.Aged between 10 and 60 years.\n* 2.Diagnosed with a discoid meniscus injury, confirmed by both magnetic resonance imaging (MRI) and arthroscopy.\n* 3.Underwent arthroscopic partial meniscectomy (saucerization) with concomitant suture repair.\n* 4.Willing to participate in the clinical trial and comply with the follow-up protocol.\n\nExclusion Criteria:\n\n* 1.Presence of concomitant injuries in the same knee, such as ligament tears, fractures, or cartilage lesions.\n* 2.Kellgren \\& Lawrence osteoarthritis grade greater than II.\n* 3.History of trauma or surgery in other weight-bearing joints of the lower limb (e.g., ankle ligament tears, osteonecrosis of the femoral head) that could indirectly affect knee joint loading and movement.","ALL","10 Years","60 Years",{"count":51,"type":52},60,"ESTIMATED","INTERVENTIONAL",[55],"NA","This study is designed as a single-center, prospective, randomized controlled trial. The aim of this clinical trial is to evaluate the effectiveness, safety, and feasibility of a wearable device-based telerehabilitation approach for postoperative recovery in patients undergoing arthroscopic surgery for discoid meniscus injury. The core research questions to be addressed are: to compare the effects of two postoperative rehabilitation methods (clinic rehabilitation versus telerehabilitation) on knee function scores in patients after arthroscopic discoid meniscus surgery; and to compare patient satisfaction, rehabilitation adherence, and clinical benefit between the two postoperative rehabilitation interventions. Participants will be randomly assigned to either the clinic rehabilitation group or the telerehabilitation group. The telerehabilitation group will undergo digital rehabilitation using wearable devices and a telerehabilitation system postoperatively, while the clinic rehabilitation group will receive one-on-one exercise rehabilitation sessions in an outpatient setting. Both groups will be followed up for six months postoperatively, with assessments scheduled at multiple time points: preoperatively, and at 2 weeks, 6 weeks, 12 weeks, and 24 weeks postoperatively. The primary outcome measures focus on clinical functional improvement, including range of motion (ROM), weight-bearing progression, muscle strength, swelling, limb circumference, functional scores (Visual Analog Scale \\[VAS\\] for pain, Tegner activity scale, International Knee Documentation Committee \\[IKDC\\] subjective form, Lysholm knee score, Ikeuchi meniscus postoperative functional score), three-dimensional gait analysis parameters, and return-to-sports evaluation. Secondary outcomes include patient satisfaction, rehabilitation adherence, imaging findings, and complication assessment.",[58],"Discoid Meniscus of Knee",[60,61,62],"telerehabilitation","wearable device","discoid meniscus","NOT_YET_RECRUITING","2026-04-18",{"date":66,"type":67},"2026-04-24","ACTUAL",{"date":69,"type":52},"2026-05-01",{"date":71,"type":52},"2028-03-31",{"name":5,"class":6}]