Effect of Telerehabilitation on Quality of Life, Pain, and Function After Rotator Cuff Surgery (TELERO-ROT)

Aysan Yaghoubi

Status: Completed

Conditions: Rotator Cuff Tears

Treatments: Other: Conventional physiotherapy program; Other: Telerehabilitation exercise program

Study type: Interventional

Funder types: Other

Identifiers

NCT07205094

AYSAN2025-RCT

Details and patient eligibility

About

he purpose of this study was to find out whether telerehabilitation after rotator cuff surgery can help reduce pain, improve shoulder movement, increase muscle strength, enhance functional ability, and improve quality of life compared to conventional physiotherapy. The study included 30 participants who had undergone rotator cuff surgery at least six weeks earlier. They were divided into two groups: a telerehabilitation group (n=20) and a conventional physiotherapy control group (n=10). Both groups followed an eight-week exercise program, which included range of motion, stretching, strengthening, and stabilization exercises.

The study found that both groups improved in pain, shoulder mobility, muscle strength, function, and quality of life. Participants in the telerehabilitation group showed particularly greater improvements in shoulder flexion, flexor muscles, external rotator muscles, and overall quality of life. These results suggest that telerehabilitation may be an effective alternative to traditional physiotherapy after rotator cuff surgery.

Enrollment: 30 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Individuals who have undergone rotator cuff surgery
• At least 6 weeks post-surgery
• Possess the necessary technology for telerehabilitation (smartphone, computer, internet access)
• Willing to participate in the study and have signed the informed consent form

Exclusion criteria

• History of neurological disorders
• Severe cardiovascular or pulmonary conditions
• Need for special medical care due to postoperative infection or complications
• Inability to comply with telerehabilitation due to psychiatric conditions
• Lack of access to or knowledge of technology required for telerehabilitation
• Participation in another rehabilitation program during the study period

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

30 participants in 2 patient groups

Telerehabilitation

Experimental group

Description:

8-week telerehabilitation program including range of motion, stretching, strengthening, and stabilization exercises

Treatment:

Other: Telerehabilitation exercise program

Conventional Physiotherapy

Active Comparator group

Description:

8-week conventional face-to-face physiotherapy program including range of motion, stretching, strengthening, and stabilization exercises

Treatment:

Other: Conventional physiotherapy program