Empowered Relief® for Cancer Survivors With Chronic Pain
Feasibility and Preliminary Efficacy of Empowered Relief® for Cancer Survivors With Chronic Pain
研究概览
详细说明
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Sophia You, PhD, ABPP
- 电话号码:918-660-3923
- 邮箱:Dokyoung-You@ou.edu
研究联系人备份
- 姓名:Jordan Keast, BS
- 邮箱:jordan-keast@ou.edu
学习地点
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Oklahoma
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Tulsa、Oklahoma、美国、74135
- 招聘中
- University of Oklahoma Schusterman Center - Tulsa
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接触:
- Jordan Keast, BS
- 邮箱:jordan-keast@ou.edu
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
History of cancer diagnosis, completion of active cancer treatment, cancer free at the time of enrollment, experience of body pain most or every day, pain duration at least 3 months, and English fluency.
Exclusion Criteria:
Significant psychological and cognitive impairment that limits one's ability to complete study tasks (completion of online survey, attending the zoom-based ER class). Life-threatening acute illness (e.g., infection, heart attack, injury), and no access to a computer, a smartphone or a tablet.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Empowered Relief
Participants in this arm of the study will complete the one-time 2hr Empowered Relief zoom course.
They will also complete a post-course survey as well as the standardized 1, 2, and 3-month follow-up surveys.
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This is a one-time 2 hour long skills-based pain management class delivered by certified instructors.
Participants learn three core pain relief skills, develop a personalized plan, and receive access to a free binaural audio app for daily use and supportive daily text messages.
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无干预:Wait-List Control
Participants in the Wait-List Control (WLC) arm will not have initial access to the empowered relief course. Additionally they will not have to complete a post-course survey. The WLC group will be asked to complete the 1, 2, and 3-month follow-up studies after no intervention. After this 3-month observatory period, WLC participants will have voluntary access to the Empowered Relief course. |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Overall treatment satisfaction
大体时间:Immediately after intervention
|
0-10 scale, higher scores indicate greater satisfaction, mean should be 8 or higher
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Immediately after intervention
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Pain Intensity
大体时间:1 month after intervention
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0-10 scale, higher scores indicate higher pain
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1 month after intervention
|
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Pain Interference
大体时间:1 month after intervention
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T-scores, higher scores indicate higher pain interference
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1 month after intervention
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Pain Intensity
大体时间:3 months after intervention
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0-10 Scale, higher scores indicate higher pain
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3 months after intervention
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Pain Interference
大体时间:3 months after intervention
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T-scores, higher scores indicate higher pain interference
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3 months after intervention
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合作者和调查者
调查人员
- 首席研究员:Sophia You, PhD, ABPP、University of Oklahoma
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- 18957P
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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