Rotator Cuff Disease
Conditions
Keywords
rotator cuff, clinical significance, minimal important chance, substantial clinical benefit, patient acceptable symptomatic state, maximal outcome improvement, Shoulder Disability Questionnaire, Western Ontario Rotator Cuff Index, Shoulder Rating Questionnaire, University of California-Los Angeles Shoulder Scale
Brief 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?
Interventions
OTHERExercise
Patients with rotator cuff disease will receive exercise treatment for two months.
Sponsors
Kırklareli University
Study design
Observational model
CASE_ONLY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Functional level | before the treatment and within 1 week after 2 months of treatment | Shoulder Disability Questionnaire (total score between 0-100) (higher values indicate higher disability) |
Countries
Turkey (Türkiye)
Contacts
CONTACTOzan Gür, MSc
PRINCIPAL_INVESTIGATOROzan Gür, MSc
Kırklareli University
Outcome results
None listed