About this trial
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 criteria
Qualifiers
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;
Disqualifiers
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;
Trial design
Treatments tested in this trial
- Wearable device rehabilitation
- Offline Traditional Rehabilitation