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RECRUITING
NCT07412184
NA

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

Sponsor: Peking University Third Hospital

View on ClinicalTrials.gov

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.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

72

Start Date

2026-01-23

Completion Date

2027-12-31

Last Updated

2026-03-10

Healthy Volunteers

No

Interventions

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

Locations (1)

Peking University Third Hospital

Beijing, China