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Recruiting NCT07324343

Which Patient Group Shows Greater Improvement With Patient Education Alone in Rotator Cuff-Related Shoulder Pain? - A Cohort Study

Conditions: Shoulder Pain Syndrome, Subacromial Pain Syndrome, Rotator Cuff Related Shoulder Pain, Patient Education

Sex: All
Ages: 18 Years – 65 Years
Healthy volunteers: No
Phase: NA
Enrollment: 116
Sponsor: Istanbul University - Cerrahpasa

Location: İstanbul University Cerrahpasa Faculty of Health Sciences, İstanbul Istanbul

Summary

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

Inclusion Criteria: * 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 * Cognitively able to understand the education and provide written informed consent Exclusion Criteria: * 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 * Pain persisting for more than 12 months

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07324343). StuddyBuddy aggregates publicly available trial information.