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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorIstanbul University - Cerrahpasa

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

Treatment groups

116 Participants
are divided into 1 treatment group