Effect of Telerehabilitation on Quality of Life, Pain, and Function After Rotator Cuff Surgery
NCT ID: NCT07205094
Last Updated: 2025-10-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
30 participants
INTERVENTIONAL
2025-02-28
2025-05-02
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Telerehabilitation in Individuals With Rotator Cuff Tear
NCT05904249
Investigation of the Effect of Motor Control Exercises in Patients Undergoing Rotator Cuff Surgery
NCT06156423
Investigation of the Efficacy of Telerehabilitation in Patients With Rotator Cuff Tendinopathy
NCT06024551
Effectiveness of Video-Based Rehabilitation Program on Pain, Functionality and Quality of Life in the Treatment of Rotator Cuff Tears
NCT03373799
Multimodal Physical Therapy With Exercise in Partial-thickness Rotator Cuff Tears
NCT03597490
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Telerehabilitation
8-week telerehabilitation program including range of motion, stretching, strengthening, and stabilization exercises
Telerehabilitation exercise program
8-week telerehabilitation program including range of motion, stretching, strengthening, and stabilization exercise
Conventional Physiotherapy
8-week conventional face-to-face physiotherapy program including range of motion, stretching, strengthening, and stabilization exercises
Conventional physiotherapy program
8-week conventional face-to-face physiotherapy program including range of motion, stretching, strengthening, and stabilization exercises
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Telerehabilitation exercise program
8-week telerehabilitation program including range of motion, stretching, strengthening, and stabilization exercise
Conventional physiotherapy program
8-week conventional face-to-face physiotherapy program including range of motion, stretching, strengthening, and stabilization exercises
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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
18 Years
65 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Aysan Yaghoubi
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Aysan Yaghoubi
Master's Graduate in Physiotherapy and Rehabilitation
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Beykent University Hospital
Istanbul, Istanbul, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Informed Consent Form
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
AYSAN2025-RCT
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.