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Clinical Trials in Turkey / NCT06677320
Recruiting Observational

Establishing Clinical Significance in Rotator Cuff Disease

NCT06677320 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2025-03-03
Last updated
2026-08-13

Condition(s) studied

Rotator Cuff Disease

Investigational drug(s) / intervention(s)

Exercise

Exercise: Patients with rotator cuff disease will receive exercise treatment for two months.

Study summary

The goal of this observational study is to learn about rotator cuff patients. The main questions it aims to answer are:

* What is the minimal clinically important difference value of the Shoulder Disability Questionnaire, the short version of the Western Ontario Rotator Cuff Index, the Shoulder Rating Questionnaire, and the University of California-Los Angeles Shoulder Scale?
* What is the substantial clinical benefit value of the Shoulder Disability Questionnaire, the short version of the Western Ontario Rotator Cuff Index, the Shoulder Rating Questionnaire, and the University of California-Los Angeles Shoulder Scale?
* What is the patient-acceptable symptomatic state value of the Shoulder Disability Questionnaire, the short version of the Western Ontario Rotator Cuff Index, the Shoulder Rating Questionnaire, and the University of California-Los Angeles Shoulder Scale?
* What is the maximal outcome improvement value of the Shoulder Disability Questionnaire, the short version of the Western Ontario Rotator Cuff Index, the Shoulder Rating Questionnaire, and the University of California-Los Angeles Shoulder Scale?
* What are the risk factors that prevent rotator cuff patients from reaching the minimal clinically important difference value?
* What are the risk factors that prevent rotator cuff patients from reaching the substantial clinical benefit value?
* What are the risk factors that prevent rotator cuff patients from reaching the patient-acceptable symptomatic state value?
* What are the risk factors that prevent rotator cuff patients from reaching the maximal outcome improvement value?

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * to be over 18 years old * to be a rotator cuff patient Exclusion Criteria: * to have another pathology in the affected shoulder area * to have a neurological, rheumatological, or oncological disease * to have radiculopathy * to have had a previous fracture or operation in the affected shoulder area * to be not cooperative enough for what will be done within the scope of the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kırklareli Eğitim ve Araştırma Hastanesi Kırklareli Turkey (Türkiye) Recruiting

More Kırklareli University trials in Turkey

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06677320 on ClinicalTrials.gov ↗ ← All trials in Turkey