Central Sensitization and Functional Outcomes in Chronic Shoulder Pain

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorPamukkale University

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

59 Participants
are divided into 1 treatment group

Locations

1
Burdur Mehmet Akif Ersoy Üniversitesi19300, BurdurTürkiye, Turkey (Türkiye)

Sponsors and collaborators

Pamukkale University

Lead sponsor

Burdur Mehmet Akif Ersoy University

Sponsor institution