Brief Behavioral Intervention for Pain (Shepherd's Hope)
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 111
- 试验地点
- 1
- 主要终点
- Change in Pain Unpleasantness Numeric Rating Scale
研究概览
简要总结
This is a single-site, two-arm, parallel-group randomized clinical trial (RCT). The clinical effects of a 4-minute audio-recorded mindfulness intervention for 100 English-speaking patients and 100 Spanish-speaking patients at a free acute care clinic will be investigated relative to a 4-minute audio-recoding about pain psychoeducation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Triple (Participant, Investigator, 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
- 是
入选标准
- •Seeking treatment at the Shepherd's Hope Downtown Clinic
排除标准
- •Cognitive impairment preventing completion of study procedures.
- •Other unstable illness judged by medical staff to interfere with study involvement.
研究组 & 干预措施
Pain Coping Information
Participants will be randomized to listen to a 4-minute audio recording providing common pain coping techniques (e.g., ice, rest, medication, surgery).
干预措施: Pain Coping Information (Behavioral)
Mindful Pain Management
Participants will be randomized to listen to a 4-minute audio recording consisting of a 1-minute introduction to mindfulness followed by a 1-minute and 30-second mindful breathing practice and a 1-minute and 30-second mindfulness of pain practice.
干预措施: Mindful Pain Management (Behavioral)
结局指标
主要结局
Change in Pain Unpleasantness Numeric Rating Scale
时间窗: Immediately before to after 4-minute audio recording
Single Likert scale item ranging from 0-10, with 0 indicating no pain and 10 representing the most unpleasant pain imaginable.
次要结局
- Change in Anxiety Numeric Rating Scale(Immediately before to after 4-minute audio recording)
- Change in Pain Intensity Numeric Rating Scale(Immediately before to after 4-minute audio recording)
研究者
Adam Hanley
Principal Investigator
Florida State University