About this trial
This prospective observational cohort study aims to investigate whether baseline central sensitization and psychological factors predict functional outcomes following rehabilitation in individuals with chronic shoulder pain. Participants with chronic shoulder pain will receive a standardized 6-week physiotherapy and rehabilitation program routinely applied in the clinic. Assessments will be performed before and after treatment, including pain severity, shoulder function, central sensitization symptoms, and psychological factors such as pain catastrophizing. The findings of this study may contribute to a better understanding of biopsychosocial factors affecting rehabilitation outcomes in chronic shoulder pain and help improve individualized rehabilitation approaches.
Eligibility criteria
Qualifiers
Adults aged 18 years and older
Presence of chronic shoulder pain lasting at least 3 months
Clinical findings consistent with shoulder-related pain
Willingness to participate in a 6-week physiotherapy rehabilitation program
Disqualifiers
History of shoulder surgery within the previous 6 months
Major shoulder trauma within the previous 6 months
Serious pathology affecting the shoulder (e.g., infection, tumor, systemic inflammatory disease)
Neurological disorders affecting the upper extremity (e.g., cervical radiculopathy, myelopathy, peripheral nerve injury)
Trial design
Treatments tested in this trial
- Physiotherapy Rehabilitation Program
Treatment groups
Sponsors and collaborators
Pamukkale University
Lead sponsor
Burdur Mehmet Akif Ersoy University
Sponsor institution