A Pilot Study Comparing Two Rehabilitation Approaches for Individuals With Irritable Shoulder Pain
Completed · Not applicable
Conditions studied: Shoulder Pain
In brief
This pilot study will assess feasibility and obtain preliminary effects of a tissue based intervention to a biopsychosocial intervention in individuals with shoulder pain.
Key facts
- Study ID
- NCT06467123
- Run by
- University of Central Florida
- People needed
- 24
- Starts
- 2024-06-28
- Expected to finish
- 2025-02-28
- Last updated by the study team
- 2025-03-05
Who can join
Age: 18 and older, up to 60. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Shoulder pain intensity rated as 3/10 or higher in the past 24 hours
You may not qualify if…
- Non-English speaking
- Systemic medical conditions that affect sensation, such as uncontrolled diabetes
- History of shoulder surgery or fracture within the past 6 months
- blood clotting disorder, such as hemophilia
- contraindication to the application of ice ((blood pressure > 140/90 mmHg, cold urticaria, cryogobulinemia, paroxysmal cold hemoglobinuria, circulatory compromise)
- Unable to exercise without a medical clearance (assessed on the PAR-Q+ on the first visit)
- Exceed pressure and sensory safety thresholds (assessed on the first visit)
- Categorized as low irritability (assessed on the first visit)
- currently pregnant
- currently receiving physical therapy to treat shoulder pain
Where it is running
- University of Central Florida — Orlando, Florida, United States
Full record on ClinicalTrials.gov
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