The Efficacy and Safety of Utilizing Mobile Phone and Motion Detector For Telerehabilitation After Arthroscopic Surgery of Rotator Cuff Tear: Single-center, Prospective Randomized Controlled Trial

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000030150

Enrollment

Unknown

Registered

2020-02-24

Start date

2020-03-01

Completion date

Unknown

Last updated

2020-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

rotator cuff tear

Interventions

experimental group:utilizing mobile phone and action detector for telerehabilitation

control group:outpatient and manual rehabilitation

Eligibility

Sex/Gender

All

Age

16 Years to 64 Years

Inclusion criteria

Inclusion criteria: (1)Aged between 16 and 64 years, owing a mobile phone (2)Agreed to receive arthroscopic repair of rotator cuff (3)Diagnosed as small to medium full-thickness rotator cuff tear(less than 3cm), with imaging support (4)Living at least 100 km or a 2 hours drive away from the hospitals (5)Signed the informed consent.

Exclusion criteria

Exclusion criteria: (1)Diagnosed as tuberculosis, shoulder joint infection and tumor patients. (2)Those who accepted rotator cuff repair or other major shoulder joint surgeries before this trial. (3)Patients with large or massive rotator cuff tear(more than 3cm) or other shoulder joint injury as SLAP injuryBankart injury. (4)Patients with shoulder duskinesia. (5)Those who could not complete the rehabilitation exercise because of mental retardation or other reasons.

Design outcomes

Secondary

Measure	Time frame
ROM;VAS;EQ-5D;UCLA;rate of retear;	—

Primary

Measure	Time frame
ASES;	—

Countries

China

Contacts

Public ContactJingyi Hou

Department of Orthopedics, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University

houjingyi246@126.com+86 15920530546

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026