跳至主要内容
临床试验/NCT05877521
NCT05877521进行中(未招募)2 期

Adapting Mindfulness-oriented Recovery Enhancement (MORE) for Cancer Pain Relief: The MORE Relief Trial

Memorial Sloan Kettering Cancer Center2 个研究点 分布在 1 个国家目标入组 76 人开始时间: 2023年5月16日最近更新:
适应症

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
2
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

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

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

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验