Effect of Telerehabilitation on Quality of Life, Pain, and Function After Rotator Cuff Surgery

NCT ID: NCT07205094

Last Updated: 2025-10-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-02-28

Study Completion Date

2025-05-02

Brief Summary

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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.

Detailed Description

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Conditions

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Rotator Cuff Tears

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Participants were assigned to two groups: a telerehabilitation group (n=20) and a conventional physiotherapy control group (n=10). Both groups followed an eight-week exercise program, including range of motion, stretching, strengthening, and stabilization exercises. Outcomes such as pain, shoulder mobility, muscle strength, functional ability, and quality of life were compared between the groups.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Telerehabilitation

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

Group Type EXPERIMENTAL

Telerehabilitation exercise program

Intervention Type OTHER

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

Group Type ACTIVE_COMPARATOR

Conventional physiotherapy program

Intervention Type OTHER

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

Interventions

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Telerehabilitation exercise program

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

Intervention Type OTHER

Conventional physiotherapy program

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

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Aysan Yaghoubi

OTHER

Sponsor Role lead

Responsible Party

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Aysan Yaghoubi

Master's Graduate in Physiotherapy and Rehabilitation

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Beykent University Hospital

Istanbul, Istanbul, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Provided Documents

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Document Type: Informed Consent Form

View Document

Other Identifiers

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AYSAN2025-RCT

Identifier Type: -

Identifier Source: org_study_id

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