Adaptation of Mindfulness Training to Treat Chronic Pain in the Military
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 14
- 试验地点
- 1
- 主要终点
- Chronic Pain - Pain Interference
研究概览
简要总结
The overall aim of this study is to test the acceptability and feasibility of an interactive, web-based mindfulness training with active duty soldiers being treated for chronic pain.
详细描述
The overall aim of study is to test the acceptability and feasibility of an interactive, web-based mindfulness training with active duty soldiers being treated for chronic pain. We will adapt the evidence-based Mindfulness-based Stress Reduction (MBSR) training for use with this population. The adapted training will be enhanced by mobile applications (apps) for skills practice, using an existing apps platform.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
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
- •Adult patients who have experienced chronic pain for at least 6 months
排除标准
- •Do not have any of the following conditions: substance abuse or dependence, psychosis, suicidal ideation in the last 2 months, high levels of trauma symptoms,
- •plans to have a permanent change of station or deploy in the coming 6 months, or
- •pregnancy
研究组 & 干预措施
Mindfulness training
6 90-minute sessions interactive, web-based mindfulness training complemented with mobile application
干预措施: Mindfulness Training (Behavioral)
结局指标
主要结局
Chronic Pain - Pain Interference
时间窗: 6 - 8 weeks post-treatment
Assess pain intensity using the Patient Reported Outcomes Measurement Information System (PROMIS) Short Form (SF) v.1.0 - Pain Interference 8a
Chronic Pain
时间窗: 6 - 8 weeks post-treatment
Assess intensity of sensory and affective pain using Short-Form McGill Pain Questionnaire
Chronic Pain - Pain Intensity
时间窗: 6 - 8 weeks post-treatment
Assess pain intensity using the Patient Reported Outcomes Measurement Information System (PROMIS) Short Form (SF) v.1.0 - Pain Intensity 3a
Chronic Pain
时间窗: Baseline
Assess intensity of sensory and affective pain using Short-Form McGill Pain Questionnaire
Chronic Pain - Pain Intensity
时间窗: Baseline
Assess pain intensity using the Patient Reported Outcomes Measurement Information System (PROMIS) Short Form (SF) v.1.0 - Pain Intensity 3a
Chronic Pain - Pain Interference
时间窗: Baseline
Assess pain intensity using the Patient Reported Outcomes Measurement Information System (PROMIS) Short Form (SF) v.1.0 - Pain Interference 8a
次要结局
- Co-Occurring Conditions - Post Traumatic Stress Disorder(6 - 8 weeks post-treatment)
- Co-Occurring Conditions - Prescription drug misuse(6 - 8 weeks post-treatment)
- Co-Occurring Conditions - Anxiety(6 - 8 weeks post-treatment)
- Quality of Life - Physical Functioning(6 - 8 weeks post-treatment)
- Co-Occurring Conditions - Alcohol Use(6 - 8 weeks post-treatment)
- Quality of Life - Sleep disturbance(6 - 8 weeks post-treatment)
- Quality of Life - Fatigue(6 - 8 weeks post-treatment)
- Self-Regulation - Pain Catastrophizing Scale(6 - 8 weeks post-treatment)
- Self-Regulation - Chronic Pain Acceptance Scale(6 - 8 weeks post-treatment)
- Co-Occurring Conditions - Depression(6 - 8 weeks post-treatment)
- Quality of Life - Role satisfaction(6 - 8 weeks post-treatment)
- Self-Regulation - Emotional Behavioral Dysregulation(6 - 8 weeks post-treatment)
- Mindfulness(6 - 8 weeks post-treatment)
- Self-Regulation - Chronic Pain Acceptance Scale(Baseline)
- Co-Occurring Conditions - Depression(Baseline)
- Co-Occurring Conditions - Anxiety(Baseline)
- Co-Occurring Conditions - Alcohol Use(Baseline)
- Co-Occurring Conditions - Post Traumatic Stress Disorder(Baseline)
- Co-Occurring Conditions - Prescription drug misuse(Baseline)
- Quality of Life - Physical Functioning(Baseline)
- Quality of Life - Sleep disturbance(Baseline)
- Quality of Life - Fatigue(Baseline)
- Quality of Life - Role satisfaction(Baseline)
- Self-Regulation - Pain Catastrophizing Scale(Baseline)
- Self-Regulation - Emotional Behavioral Dysregulation(Baseline)
- Mindfulness(Baseline)