NCT07412184

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

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 72 (estimated)
• Sponsor: Peking University Third Hospital · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

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.

Detailed description

In this randomized controlled clinical study, patients with unilateral rotator cuff tears were included. Starting from the fifth week after surgery, they were randomly assigned to either an online wearable device training group or an offline traditional rehabilitation group, with analyses conducted through functional tests and assessments. The study investigated the impact of wearable device rehabilitation on functional recovery in patients with rotator cuff tears and compared it with offline traditional rehabilitation to verify its efficacy.

Conditions

• Rotator Cuff Tear

Interventions

Type	Name	Description
DEVICE	Wearable device rehabilitation	Patients with rotator cuff tears wear sensors and undergo training in conjunction with 'Fugu Medical'.
OTHER	Offline Traditional Rehabilitation	Offline Traditional Rehabilitation

Timeline

• Start date: 2026-01-23
• Primary completion: 2027-12-31
• Completion: 2027-12-31
• First posted: 2026-02-17
• Last updated: 2026-03-10

Locations

1 site across 1 country: China