NCT06467123
Completed
N/A
A Pilot Study Comparing Two Rehabilitation Approaches for Individuals With Irritable Shoulder Pain
ConditionsShoulder Pain
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Shoulder Pain
- Sponsor
- University of Central Florida
- Enrollment
- 24
- Locations
- 1
- Primary Endpoint
- Report preliminary outcomes of treatment effects
- Status
- Completed
- Last Updated
- last year
Overview
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.
Investigators
Abigail Wilson
Assistant Professor
University of Central Florida
Eligibility Criteria
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
Outcomes
Primary Outcomes
Report preliminary outcomes of treatment effects
Time Frame: 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
Time Frame: through study completion, 4 weeks
Number of participants who complete the study and adverse events will be reported
Study Sites (1)
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