A Pilot Study Comparing Two Rehabilitation Approaches for Individuals With Irritable Shoulder Pain
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 24
- 试验地点
- 1
- 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
研究组 & 干预措施
Tissue Intervention
Participants will attend eight sessions. During each session, participants will receive education on positions of comfort, progressing activities, and return to function. Participants will complete shoulder stretching and strengthening exercises according to a protocol.
干预措施: Tissue Intervention (Other)
Biopsychosocial Intervention
Participants will attend eight sessions. During each session, participants will receive education on pain neuroscience education, stress management, and maintaining physical activity. Participants will complete shoulder stretching and strengthening exercises according to a graded exercise protocol.
干预措施: Biopsychosocial Intervention (Other)
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