[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100624634":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":30,"centralContacts":35,"locations":40,"responsibleParty":52,"collaborators":26,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":58,"acronym":26,"eligibilityCriteria":59,"healthyVolunteers":56,"sex":60,"minAge":61,"maxAge":26,"enrollmentInfo":62,"targetDuration":26,"studyType":65,"phases":66,"briefSummary":68,"conditions":69,"keywords":71,"overallStatus":42,"whyStopped":26,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":84},{"fullName":5,"class":6},"Peking University Third Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Online Wearable Device Training Group","EXPERIMENTAL","The online wearable device training group trained independently using wearable sensor devices according to the 'Fugu Medical Mini Program' instructions. Training started from the 5th week post-surgery and continued until the 12th week, totaling 8 weeks, with a minimum of 3 training days per week and 50 minutes each day.",[13],"Device: Wearable device rehabilitation",{"label":15,"type":16,"description":17,"interventionNames":18},"Offline Traditional Rehabilitation Group","ACTIVE_COMPARATOR","The offline traditional rehabilitation group carries out rehabilitation training under the guidance of therapists. Starting from the 5th week post-surgery and continuing until the 12th week, the training lasts for a total of 8 weeks, with at least 3 sessions per week, each lasting 50 minutes.",[19],"Other: Offline Traditional Rehabilitation",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","Wearable device rehabilitation","Patients with rotator cuff tears wear sensors and undergo training in conjunction with 'Fugu Medical'.",[9],null,{"type":6,"name":28,"description":28,"armGroupLabels":29,"otherNames":26},"Offline Traditional Rehabilitation",[15],[31],{"name":32,"affiliation":33,"role":34},"Shuang Ren, Doctor","Affiliated with the organization","STUDY_CHAIR",[36],{"name":32,"role":37,"phone":38,"phoneExt":26,"email":39},"CONTACT","17610252992","xixishuang123@126.com",[41],{"facility":5,"status":42,"city":43,"state":26,"zip":26,"country":44,"countryCode":45,"cosmosGeoPoint":46,"geoPoint":51,"contacts":26},"RECRUITING","Beijing","China","CN",{"type":47,"coordinates":48},"Point",[49,50],116.39723,39.9075,{"lat":50,"lon":49},{"type":53,"investigatorFullName":26,"investigatorTitle":26,"investigatorAffiliation":26,"oldNameTitle":26,"oldOrganization":26},"SPONSOR","100624634","research-and-clinical-validation-of-a-wearable-device-based-remote-rehabilitation-system-for-postoperative-rotator-cuff-injury-100624634",false,"NCT07412184","Research and Clinical Validation of a Wearable Device-Based Remote Rehabilitation System for Postoperative Rotator Cuff Injury","Inclusion Criteria:\n\n* Age ≥18 years;\n* First-time rotator cuff injury surgery and received surgical treatment at Peking University Third Hospital;\n* MRI shows a tear with a maximum diameter \\\u003C3 cm, confirmed by at least three musculoskeletal rehabilitation radiologists;\n* Possess a mobile device with internet access (e.g., smartphone or tablet) capable of using mobile applications;\n* Able to complete the planned study and follow-ups within 6 months after discharge;\n* No visual, hearing, cognitive, or communication impairments;\n* Able to provide informed and valid consent to participate in the study.\n\nExclusion Criteria:\n\n* Presence of serious cardiovascular or cerebrovascular diseases, or cervical spondylosis with nerve damage;\n* Presence of cognitive impairment or vision problems;\n* Stroke, rheumatic disease, neurological disorders, or diseases limiting overall physical function or cardiopulmonary function within the past 2 years;\n* No prior history of shoulder joint injury, and having undergone other surgeries within the past 6 months;\n* Patients who cannot complete the entire cycle or drop out midway;\n* Presence of serious postoperative complications, such as wound infection, venous thromboembolism, etc.","ALL","18 Years",{"count":63,"type":64},72,"ESTIMATED","INTERVENTIONAL",[67],"NA","This study included patients who underwent their first shoulder rotator cuff surgery at Peking University Third Hospital, diagnosed with small to medium rotator cuff tears based on MRI results. Participants were randomly divided into an online wearable device training group and an offline traditional rehabilitation group, with 36 individuals in each group. Before testing began, patients were ensured to participate voluntarily and had signed informed consent forms.",[70],"Rotator Cuff Tear",[72,73,74],"Rotator cuff tear","Wearable device","Remote rehabilitation","2026-03-08",{"date":77,"type":78},"2026-03-10","ACTUAL",{"date":80,"type":78},"2026-01-23",{"date":82,"type":64},"2027-12-31",{"name":5,"class":6},1]