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临床试验/NCT01487473
NCT01487473已完成不适用

The Effects of Mindfulness-Based Stress Reduction on Attention and Pain-related Symptoms in Chronic Pain Patients: A Randomized Controlled Trial

York University2 个研究点 分布在 1 个国家目标入组 49 人开始时间: 2011年12月最近更新:
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适应症

试验速览

阶段
不适用
状态
已完成
入组人数
49
试验地点
2
主要终点
Pain disability and Attention
研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The main purpose of this study is to determine the degree to which Mindfulness-Based Stress Reduction, a group-based psychological therapy that includes mindfulness meditation exercises, reduces depression, anxiety, stress, pain intensity, and interference of pain with daily life among adult chronic pain patients.

The second purpose is to examine the role of attention in improving psychological and physical health for chronic pain patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Investigator)

入排标准

年龄范围
18 Years 至 80 Years（Adult, Older Adult）
性别
All
接受健康志愿者
否

入选标准

  • •Adult chronic pain patients who are proficient in English
  • •Capable of interacting with others in a group setting
  • •Capable of working with a computer

排除标准

  • •Alcohol or drug abuse (past history is acceptable as long as their situation has been stable for at least 3 months)
  • •Psychiatric psychosis (patients who have a past history of schizophrenia are eligible as long as they are currently stable)
  • •Current major depressive disorder
  • •Current severe social phobia
  • •At immediate risk for suicide
  • •Cerebral lesions or tumors (unless medically and cognitively stable)
  • •Neurological disease
  • •Medically unstable
  • •Cognitively unstable
  • •Previously participated in a mindfulness meditation program

结局指标

主要结局

Pain disability and Attention

时间窗: Baseline, immediately following treatment, and at 3 months follow up

Change in pain disability assessed by the Pain Disability Index (PDI). Change in attention assessed by an adapted version of the Change Blindness Task

次要结局

  • Stress(Baseline, immediately following treatment, and at 3 months follow up)
  • Acceptance(Baseline, immediately following treatment, and at 3 months follow up)
  • Pain Intensity(Baseline, immediately following treatment, and at 3 months follow up)
  • Depression(Baseline, immediately following treatment, and at 3 months follow up)
  • Anxiety(Baseline, immediately following treatment, and at 3 months follow up)
  • Mindfulness(Baseline, immediately following treatment, and at 3 months follow up)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nicholas Cepeda

Associate Professor

York University

研究点 (2)

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