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?
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Functional level
Timeframe: before the treatment and within 1 week after 2 months of treatment
Functional level
Timeframe: before the treatment and within 1 week after 2 months of treatment
Functional level
Timeframe: before the treatment and within 1 week after 2 months of treatment
Functional level
Timeframe: before the treatment and within 1 week after 2 months of treatment