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Clinical Trials in Turkey / NCT07654023
Starting soon Observational

Central Sensitization and Functional Outcomes in Chronic Shoulder Pain

NCT07654023 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-06-15
Last updated
2026-06-17

Condition(s) studied

Chronic Shoulder Pain

Investigational drug(s) / intervention(s)

Physiotherapy Rehabilitation Program

Physiotherapy Rehabilitation Program: A standardized 6-week exercise-based physiotherapy and rehabilitation program routinely applied in clinical practice, including patient education, scapular stabilization exercises, strengthening exercises, range of motion exercises, functional training, and home exercise recommendations for individuals with chronic shoulder pain.

Study summary

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * 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 * Ability to complete study assessments and questionnaires * Provision of written informed consent Exclusion Criteria: * 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) * Severe cognitive impairment * Communication problems preventing participation * Shoulder injection within the previous 4 weeks * Pregnancy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Burdur Mehmet Akif Ersoy Üniversitesi Burdur Türkiye

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07654023 on ClinicalTrials.gov ↗ ← All trials in Turkey