Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Culturally Adapted Pain Management for Indigenous Peoples

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

Run by University of California, San Diego · NCT07524751 · Data updated 2026-11-12

A feasibility test will see if a culturally tailored pain-management program can be delivered to AI/AN adults with chronic pain at the Yakama Service Unit and pave the way for a larger trial.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment30 (estimated)
SponsorUniversity of California, San Diego
Academic / other
Locations1 site (Yakima, Washington)
StatusRecruiting
StartedJuly 8, 2026
Main results expectedJune 30, 2028
Study endsNovember 30, 2028
Registry record updatedOctober 15, 2026
Trial IDNCT07524751 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are AI/AN adults with chronic pain, who speak English, have reliable contact methods, and can participate in a behavioral program.

Probably not a fit

Patients with significant cognitive impairment, severe uncontrolled mental illness, active substance abuse, or active cancer treatment may not benefit from this specific intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized feasibility pilot examines a culturally adapted psychological intervention for chronic pain among American Indian/Alaska Native adults. Participants will be adults 18+ who identify as AI/AN and have chronic pain interfering with function, and will be randomized to receive the braided skills program. The study aims to determine whether a larger, fully powered randomized controlled trial is practical, including recruitment, retention, and preliminary outcomes. The program was developed in earlier work (K99 phase) and is now tested in a real-world clinical setting within the Portland Area Indian Health Service – Yakama Service Unit. Feasibility metrics will guide the design of a future definitive trial.

Why it matters

Potential benefit: If successful, the intervention could offer a culturally resonant approach to managing chronic pain, potentially improving function and quality of life for AI/AN patients.

How similar studies have gone: Previous work has demonstrated the value of culturally adapted psychosocial approaches in similar populations, supporting the potential benefit of this strategy.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 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

Exclusion Criteria:

* 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

Where it's running

  • Portland Area Indian Health Services - Yakama Service Unit
    Yakima, Washington, United States
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.