NCT07205094

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2025

Completed
2 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 2, 2025

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

September 24, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

October 3, 2025

Completed
Last Updated

October 3, 2025

Status Verified

October 1, 2025

Enrollment Period

2 months

First QC Date

September 24, 2025

Last Update Submit

October 1, 2025

Conditions

Keywords

Rotator Cuff SurgeryTelerehabilitation MethodPainQuality of LifeFunction

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

EXPERIMENTAL

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

Other: Telerehabilitation exercise program

Conventional Physiotherapy

ACTIVE COMPARATOR

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

Other: Conventional physiotherapy program

Interventions

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

Telerehabilitation

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

Conventional Physiotherapy

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Beykent University Hospital

Istanbul, Istanbul, 34500, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Rotator Cuff InjuriesPain

Condition Hierarchy (Ancestors)

RuptureWounds and InjuriesShoulder InjuriesTendon InjuriesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: 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.
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

Locations