Examining the Efficacy of a Single Session Mindfulness Oriented Recovery Enhancement Intervention: One MORE
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Pain Catastrophizing
研究概览
简要总结
This study will be a single-site, two-arm randomized controlled trial conducted among chronic pain patients. Chronic pain patients will be randomized by a computer-generated randomization schedule with simple random allocation (1:1) to either One MORE or a wait-list control condition (WLC). One MORE will be delivered individually via a HIPAA compliant virtual meeting platform.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •men/women ≥18 years of age
- •current chronic pain diagnosis
- •reporting pain ≥3 on 0-10 scale
排除标准
- •unstable illness judged by clinician to interfere with study participation
研究组 & 干预措施
One MORE
干预措施: One MORE (Behavioral)
Waitlist Control
结局指标
主要结局
Pain Catastrophizing
时间窗: Will be completed at baseline, week 2, and 1, 2, and 3 months after baseline.
Change in pain catastrophizing from baseline through 3-month follow-up will be assessed with the Pain Catastrophizing Scale. Scores range from 0 to 52, with higher scores reflecting greater pain catastrophizing.
次要结局
- Pain Intensity(Will be completed at baseline, week 2, and 1, 2, and 3 months after baseline.)
- Pain Interference(Will be completed at baseline, week 2, and 1, 2, and 3 months after baseline.)
研究者
Adam Hanley
Assistant Professor
University of Utah