Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07324343

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

Led by Istanbul University - Cerrahpasa · Updated on 2026-01-07

116

Participants Needed

1

Research Sites

65 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals aged 18-65 years
  • Shoulder pain lasting at least 4 weeks
  • Diagnosed by an orthopedic physician with impingement, subacromial bursitis, rotator cuff tendinopathy, or partial tear
  • Activity-related pain score of 3 or higher on the Numerical Pain Rating Scale
  • Able to understand the education and provide written informed consent
Not Eligible

You will not qualify if you...

  • History of shoulder surgery
  • Diagnosis of frozen shoulder, full-thickness or massive rotator cuff tear, or shoulder instability
  • Neurological or psychiatric conditions that prevent exercise
  • Received physical therapy, rehabilitation, or injection treatment within the last 6 months
  • Shoulder pain lasting more than 12 months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

İstanbul University Cerrahpasa Faculty of Health Sciences, İstanbul

Istanbul, Turkey (Türkiye)

Actively Recruiting

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Research Team

M

Merve KOYUNCU CENİKLİ Research asistant, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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