Effect of Telerehabilitation on Quality of Life, Pain, and Function After Rotator Cuff Surgery
TELERO-ROT
Effect of Telerehabilitation Versus Conventional Physiotherapy on Quality of Life, Pain, and Functional Outcomes in Patients Following Rotator Cuff Surgery
1 other identifier
interventional
30
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 28, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 2, 2025
CompletedFirst Submitted
Initial submission to the registry
September 24, 2025
CompletedFirst Posted
Study publicly available on registry
October 3, 2025
CompletedOctober 3, 2025
October 1, 2025
2 months
September 24, 2025
October 1, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pain intensity (Visual Analog Scale [VAS], 0-10 points)
Pain intensity was assessed before and after the 8-week intervention using the Visual Analog Scale (VAS) during activity, at rest, and at night. Scores range from 0 (no pain) to 10 (worst imaginable pain), with higher scores indicating worse pain. Changes were compared between the telerehabilitation group and the conventional physiotherapy control group.
Baseline and after 8-week intervention
Secondary Outcomes (4)
Shoulder range of motion (Goniometer, degrees)
Baseline and after 8-week intervention
Muscle strength (Manual Muscle Testing, 0-5 scale)
Baseline and after 8-week intervention
Quality of life (Western Ontario Rotator Cuff Index [WORC], 0-2100 points)
Baseline and after 8-week intervention
Functional status (Disabilities of the Arm, Shoulder, and Hand [DASH] questionnaire, 0-100 points)
Baseline and after 8-week intervention.
Study Arms (2)
Telerehabilitation
EXPERIMENTAL8-week telerehabilitation program including range of motion, stretching, strengthening, and stabilization exercises
Conventional Physiotherapy
ACTIVE COMPARATOR8-week conventional face-to-face physiotherapy program including range of motion, stretching, strengthening, and stabilization exercises
Interventions
8-week telerehabilitation program including range of motion, stretching, strengthening, and stabilization exercise
8-week conventional face-to-face physiotherapy program including range of motion, stretching, strengthening, and stabilization exercises
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Aysan Yaghoubilead
Study Sites (1)
Beykent University Hospital
Istanbul, Istanbul, 34500, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Master's Graduate in Physiotherapy and Rehabilitation
Study Record Dates
First Submitted
September 24, 2025
First Posted
October 3, 2025
Study Start
February 28, 2025
Primary Completion
April 30, 2025
Study Completion
May 2, 2025
Last Updated
October 3, 2025
Record last verified: 2025-10
Data Sharing
- IPD Sharing
- Will not share