Establishing Clinical Significance in Rotator Cuff Disease
ConditionRotator Cuff Disease
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorKırklareli University
About this trial
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 criteria
This trial does not accept healthy volunteersQualifiers
to be over 18 years old
to be a rotator cuff patient
Disqualifiers
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
Trial population
The study will be conducted with rotator cuff patients who will have physical therapy at Kırklareli Training and Research Hospital's physical therapy unit.
Trial design
Design model
Case-only
Time perspective
Prospective
Treatments tested in this trial
Exercise
Other interventionPatients with rotator cuff disease will receive exercise treatment for two months.
Treatment groups
69 Participants
are divided into 1 treatment groupGroup A: Rotator cuff patients1 intervention
Trial outcomes
Primary outcomes
1
Functional level
Shoulder Disability Questionnaire (total score between 0-100) (higher values indicate higher disability)
Time frame
before the treatment and within 1 week after 2 months of treatment2
Functional level
The short version of the Western Ontario Rotator Cuff Index (total score between 0-100) (higher values indicate higher functional level)
Time frame
before the treatment and within 1 week after 2 months of treatment3
Functional level
Shoulder Rating Questionnaire (total score between 17-100) (higher values indicate higher functional level)
Time frame
before the treatment and within 1 week after 2 months of treatment4
Functional level
The University of California-Los Angeles Shoulder Scale (total score between 0-100) (higher values indicate higher functional level)
Time frame
before the treatment and within 1 week after 2 months of treatmentSponsors and contacts
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Source ClinicalTrials.gov