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Clinical Trials/NCT06024551
NCT06024551
Completed
N/A

Investigation of the Efficacy of Telerehabilitation in Patients With Rotator Cuff Tendinopathy

Izmir Democracy University1 site in 1 country34 target enrollmentDecember 15, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Rotator Cuff Injuries
Sponsor
Izmir Democracy University
Enrollment
34
Locations
1
Primary Endpoint
Simple Shoulder Test
Status
Completed
Last Updated
last year

Overview

Brief Summary

The goal of this study is to investigate the effect of telerehabilitation in patients with rotator cuff tendinopathy. The main questions it aims to answer are:

  • Is telerehabilitation effective in improving the functional status of patients with rotator cuff tendinopathy?
  • Is telerehabilitation effective in reducing the pain of rotator cuff patients?

Detailed Description

Patients between the ages of 18-65 who were diagnosed with rotator cuff tendinopathy will be included in the study. Patients will be divided into two groups. Patients in group 1 will be given a home exercise program. Then, the patients will be called 3 times a week and it will be evaluated whether they do their exercises regularly and whether they do it correctly. At the end of the first month, the patients will be evaluated again for functionality and pain. The patients in group 2 will be given a home exercise program and at the end of the first month, the patients will be evaluated again in terms of functionality and pain.

Registry
clinicaltrials.gov
Start Date
December 15, 2023
End Date
June 15, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Izmir Democracy University
Responsible Party
Principal Investigator
Principal Investigator

Ferruh Taşpınar

Associate Professor

Izmir Democracy University

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of Rotator cuff tendinopathy
  • Being able to do the prescribed exercises
  • Having an access to internet and having a computer or smart phone for telerehabilitation

Exclusion Criteria

  • Patients with a neurological disease that may affect the effectiveness of exercise
  • History of fracture in shoulder region
  • History of surgery in shoulder region
  • Patients with a psychiatric disorder

Outcomes

Primary Outcomes

Simple Shoulder Test

Time Frame: one month

A questionnaire about the function of the involved shoulder. Overall scored is calculated by number of yes/number of completed items. Minimum score is 0 %and maximum is 100 %. Higher scores indicate better function.

Western Ontario Rotator Cuff Index

Time Frame: one month

Western Ontario Rotator Cuff Index is a disease-specific quality of life questionnaire, evaluating the change in symptoms and functional ability, specific to a Rotator Cuff tendinopathy. Raw scores range from 0 to 2100 with a higher score indicating decreased quality of life.

Secondary Outcomes

  • Range of motion(one month)

Study Sites (1)

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