Adapting Mindfulness-oriented Recovery Enhancement (MORE) for Cancer Pain Relief: The MORE Relief Trial
试验速览
- 阶段
- 2 期
- 状态
- 进行中（未招募）
- 入组人数
- 76
- 试验地点
- 1
- 主要终点
- Rate of participant enrollment to the study
研究概览
简要总结
The purpose of this study is to evaluate whether or not mindfulness-based interventions/MBIs may help reduce chronic pain in participants who have cancer-related chronic pain. MBIs are therapeutic programs that use mindfulness meditation practices to help people focus on the present moment, as well as encourage acceptance of thoughts, emotions, and body sensations. The researchers think that an MBI treatment called Mindfulness-oriented Recovery Enhancement (MORE) may help people who are experiencing cancer-related chronic 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 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •English speaking
- •Age ≥ 18 years or older
- •A history of cancer with no restrictions placed on type of cancer
- •Determined to be either no-evidence of disease or stable oncological disease by referring or study physicians/advanced practice providers
- •Having a pain (musculoskeletal, generalized, or neuropathic) rating of 4 or greater in worst pain on a 0-10 numerical rating scale in the preceding week
- •Having had pain for at least 3 months and at least 15 days with pain in the preceding 30 days
- •Willing to adhere to all study-related procedures, including randomization to one of two treatment arms: MORE or WLC
- •Ability to attend video-call session and a quiet/private location
排除标准
- •Active suicidality or schizophrenia
- •Plan to initiate palliative radiation or interventional pain procedure within the next 12 weeks
- •Cognitive impairment preventing completing PRO independently or participate in virtual MORE as evaluated by study clinicians
研究组 & 干预措施
16-hour MORE treatments
Patients in the 16-hour MORE format will receive one 2hrs treatment a week for 8 consecutive weeks (as per study schema: from week 1 to week 8).
干预措施: MORE treatments (Behavioral)
Wait List Control (WLC) Usual Care Procedure
Participants in the WLC group continue to receive their standard medical care and pain management as prescribed by their physicians or other health care providers.
干预措施: Standard of Care for Pain Management (Other)
8-hour MORE treatments
Patients in the 8-hour MORE format will receive one 2hrs treatment a week for 4 consecutive weeks (as per study schema: from week 1 to week 4).
干预措施: MORE treatments (Behavioral)
2-hour MORE treatments
Patients in the 2-hour MORE format will receive one 2hrs treatment (as per study schema: in week 1).
干预措施: MORE treatments (Behavioral)
结局指标
主要结局
Rate of participant enrollment to the study
时间窗: 12 months
Feasibility of the intervention will be determined by Rate of participant enrollment to the study
次要结局
未报告次要终点