A Pilot Study Comparing Two Rehabilitation Approaches for Individuals With Irritable Shoulder Pain
Not Applicable
Completed
- Conditions
- Shoulder Pain
- Registration Number
- NCT06467123
- Lead Sponsor
- University of Central Florida
- Brief Summary
This pilot study will assess feasibility and obtain preliminary effects of a tissue based intervention to a biopsychosocial intervention in individuals with shoulder pain.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 24
Inclusion Criteria
- Shoulder pain intensity rated as 3/10 or higher in the past 24 hours
Exclusion Criteria
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Report preliminary outcomes of treatment effects through study completion, 4 weeks Shoulder pain intensity measured with the numeric pain rating scale will be compared between groups.
Report rate of adherence and adverse effects through study completion, 4 weeks Number of participants who complete the study and adverse events will be reported
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of Central Florida
🇺🇸Orlando, Florida, United States
University of Central Florida🇺🇸Orlando, Florida, United States