Ignite Creation Date:
2025-12-24 @ 11:42 PM
Ignite Modification Date:
2025-12-24 @ 11:42 PM
Study NCT ID:
NCT06024551
Status:
COMPLETED
Last Update Posted:
2024-08-09
First Post:
2023-04-04
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Investigation of the Efficacy of Telerehabilitation in Patients With Rotator Cuff Tendinopathy
Sponsor:
Izmir Democracy University
Organization:
Study Overview
Official Title:
Investigation of the Efficacy of Telerehabilitation in Patients With Rotator Cuff Tendinopathy
Status:
COMPLETED
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
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?
* 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.
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.
Study Oversight
Has Oversight DMC:
False
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: