NCT06467123已完成不适用
A Pilot Study Comparing Two Rehabilitation Approaches for Individuals With Irritable Shoulder Pain
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 24
- 试验地点
- 2
- 主要终点
- Report preliminary outcomes of treatment effects
研究概览
简要总结
This pilot study will assess feasibility and obtain preliminary effects of a tissue based intervention to a biopsychosocial intervention in individuals with shoulder pain.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Shoulder pain intensity rated as 3/10 or higher in the past 24 hours
排除标准
- •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
结局指标
主要结局
Report preliminary outcomes of treatment effects
时间窗: 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
时间窗: through study completion, 4 weeks
Number of participants who complete the study and adverse events will be reported
次要结局
未报告次要终点
研究者
Abigail Wilson
Assistant Professor
University of Central Florida
研究点 (2)
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