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临床试验/NCT07524751
NCT07524751招募中不适用

Culturally Adapted Pain Management for Indigenous Peoples in the Pacific Northwest (CAP-I)

University of California, San Diego1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2026年6月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
1
主要终点
Recruitment

研究概览

简要总结

The proposed study involves a randomized feasibility pilot trial of a culturally adapted psychological intervention for chronic pain for American Indian/Alaska Native (AI/AN) individuals receiving care for pain at the Portland Area Indian Health Service - Yakama Service Unit. The study will provide information on whether or not it is feasible to conduct a future fully-powered randomized controlled trial.

详细描述

The prevalence of chronic pain is higher among American Indian/Alaskan Native (AI/AN) people than any other group in the United States. This proposed study aims to begin the process of developing a culturally-adapted psychological intervention for chronic pain among AI/AN individuals receiving care for pain at the Portland Area Indian Health Service - Yakama Service Unit. The K99 phase focused on the development of the intervention and the R00 entails a feasibility randomized pilot trial. The current study (i.e., the R00 phase) aims to assess the feasibility of conducting a future randomized controlled trial with the newly developed culturally-adapted psychological intervention for 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

  • at least 18 years of age
  • identify as AI/AN (or by another preferred name, such Native American, Native, and/or Indigenous)
  • have at least one diagnosis consistent with chronic pain and/or meet criteria for chronic pain diagnosis at enrollment (i.e., experience pain for > 50% in the past 3 months that interferes with daily functioning)
  • possess the ability to speak and understand English
  • have access to a mode of communication for contact, such as a telephone, for study purposes

排除标准

  • significant cognitive impairment
  • current uncontrolled serious psychological issues (e.g., schizophrenia, bipolar disorder)
  • active medical treatment for malignant conditions (e.g., cancer)
  • active suicidality with intent
  • active alcohol and/or substance abuse

研究组 & 干预措施

Treatment-as-usual

No Intervention

Study participants will proceed with their medical care as usual for chronic pain.

Active Treatment

Experimental

Treatment is group-based and remote-based. Treatment groups will include 4-6 study participants. A total of 7 treatment sessions are delivered on a weekly basis. The treatment is an integration of evidence-based psychological tools for pain management and Indigenous healing practices.

干预措施: Braided Skills for Managing Pain (Behavioral)

结局指标

主要结局

Recruitment

时间窗: Until the end of the recruitment phase (once all study participants have been recruited, an estimated 1-2 years).

Successful recruitment is defined by the randomization of 30 study participants

次要结局

  • Treatment adherence(From the start of treatment to the end of treatment at 7 weeks.)
  • Treatment satisfaction(Post-treatment assessment, conducted after completion of the 7 weeks of treatment.)
  • Cultural congruency(Post-treatment assessment, conducted after completion of the 7 weeks of treatment.)

研究者

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

Andrea K. Newman

Assistant Clinical Professor

University of California, San Diego

研究点 (1)

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