Research and Clinical Validation of a Wearable Device-Based Remote Rehabilitation System for Postoperative Rotator Cuff Injury
Peking University Third Hospital
72 participants
Jan 23, 2026
INTERVENTIONAL
Conditions
Summary
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.
Eligibility
Inclusion Criteria7
- Age ≥18 years;
- First-time rotator cuff injury surgery and received surgical treatment at Peking University Third Hospital;
- MRI shows a tear with a maximum diameter <3 cm, confirmed by at least three musculoskeletal rehabilitation radiologists;
- Possess a mobile device with internet access (e.g., smartphone or tablet) capable of using mobile applications;
- Able to complete the planned study and follow-ups within 6 months after discharge;
- No visual, hearing, cognitive, or communication impairments;
- Able to provide informed and valid consent to participate in the study.
Exclusion Criteria6
- Presence of serious cardiovascular or cerebrovascular diseases, or cervical spondylosis with nerve damage;
- Presence of cognitive impairment or vision problems;
- Stroke, rheumatic disease, neurological disorders, or diseases limiting overall physical function or cardiopulmonary function within the past 2 years;
- No prior history of shoulder joint injury, and having undergone other surgeries within the past 6 months;
- Patients who cannot complete the entire cycle or drop out midway;
- Presence of serious postoperative complications, such as wound infection, venous thromboembolism, etc.
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Interventions
Patients with rotator cuff tears wear sensors and undergo training in conjunction with 'Fugu Medical'.
Offline Traditional Rehabilitation
Locations(1)
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NCT07412184