Research and Clinical Validation of a Wearable Device-Based Remote Rehabilitation System for Postoperative Rotator Cuff Injury

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorPeking University Third Hospital

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

Treatment groups

72 Participants
are divided into 2 treatment groups