About this trial
The primary aim of this study is to determine the clinical effectiveness of patient education alone in individuals with rotator cuff-related shoulder pain and to identify which patient subgroups benefit more from this approach. In addition, the translation and cultural adaptation of the "Patient Knowledge Questionnaire (PKQ-RCRSP)" into Turkish will be carried out to measure the level of patient knowledge regarding patient education.
Eligibility criteria
Qualifiers
Individuals aged 18-65 years
Shoulder pain persisting for at least 4 weeks
Diagnosed by an orthopedic physician with impingement, subacromial bursitis, rotator cuff (RC) tendinopathy, or partial tear
Activity-related pain ≥3 on the NPRS
Disqualifiers
History of shoulder surgery
Diagnosis of frozen shoulder, full-thickness or massive rotator cuff (RC) tear, or instability
Presence of neurological or psychiatric conditions that prevent exercise
History of physical therapy-rehabilitation or injection treatment within the past 6 months
Trial design
Treatments tested in this trial
- Questionnaire Validation
- Patient Education