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临床试验/NCT01149317
NCT01149317已完成不适用

Acupuncture to Decrease Disparities in Outcomes of Pain Treatment

Albert Einstein College of Medicine2 个研究点 分布在 1 个国家目标入组 235 人开始时间: 2008年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
235
试验地点
2
主要终点
Brief Pain Inventory

研究概览

简要总结

Chronic pain is a significant public health problem, associated with impairments of physical and psychological functioning. While a third or more of the general population may suffer from chronic pain, it is often under recognized and under treated in health care settings. Low income and minority samples experience disparities in the prevalence of chronic pain, in perceived access to effective pain treatment, and in consultations for pain. A great deal of literature suggests that acupuncture offers potential benefit in the management of chronic pain, but it is rarely available to low income patients. The Acupuncture to Decrease Disparities in Outcomes of Pain Treatment (ADDOPT) project will introduce and evaluate the addition of acupuncture to the management of chronic pain for ethnically diverse, low-income primary care patients. The project represents a collaboration between the New York City Research and Improvement Networking Group (NYC RING), a practice-based research network dedicated to decreasing health disparities through primary care research, the Continuum Center for Health and Healing,The Swedish Institute School of Acupuncture, and Pacific College of Oriental Medicine. Our intervention will involve addition of weekly acupuncture sessions at 3 urban primary care practices. During training sessions at each practice, primary care providers will become familiar with acupuncture and indications for referral. Patients will be eligible if they experience chronic pain due to neck pain, back pain, or osteoarthritis. Our process evaluation, guided by Glasgow's REAIM framework, will assess barriers to implementation and adoption of the intervention in busy urban practices and acceptability to patients and providers. The investigators will employ a quasiexperimental design to assess primary outcomes (pain and quality of life) and obtain preliminary estimates of secondary outcomes (health care utilization and costs) of the intervention at each health center. This design will permit comparison across sites to discern practice level differences in uptake and outcomes.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Chronic pain due to osteoarthritis, back pain or neck pain; English or Spanish speaking

排除标准

  • Active substance abuse; cognitive impairment; coumadin therapy

结局指标

主要结局

Brief Pain Inventory

时间窗: 1 mo pre-acupuncture and 6 mo

次要结局

  • Pain Free Days(pre-acupuncture and 6 mo)
  • Pain Impact Questionnaire(1 mo pre-acupuncture and 6 mo)
  • Quality of Life(1 mo pre-acupuncture and 6 mo)

研究者

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

Diane Mckee

Associate Professor, Dept of Family and Social Medicine

Albert Einstein College of Medicine

研究点 (2)

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