Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06565416

Opioid and Pain Treatment in Indigenous Communities (OPTIC) Trial: Implementation of Screening and Brief Intervention

Led by University of New Mexico · Updated on 2025-11-12

225

Participants Needed

3

Research Sites

104 weeks

Total Duration

On this page

Sponsors

U

University of New Mexico

Lead Sponsor

N

National Institute on Drug Abuse (NIDA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating culturally tailored screening and brief intervention methods for chronic pain and opioid misuse or opioid use disorder among American Indian and Alaska Native (AI/AN) clients in three clinics serving these communities. This study addresses the health disparities and limited access to quality care for these conditions in AI/AN populations, aiming to improve provider skills and client outcomes using a culturally centered approach. The trial is a type III effectiveness-implementation study conducted over 24 months at each site. The study involves several phases: an initial baseline period, followed by a 6-month workgroup phase where clinic-specific goals are set, then a 6-month implementation phase where evidence-based strategies are practiced, and finally a sustainment phase to measure how well the clinic maintains these goals. The intervention focuses on training providers to better manage chronic pain and opioid misuse within cultural frameworks that emphasize client functioning rather than pain elimination. Participants will be involved through surveys and electronic medical record data collection to assess staff perspectives and client outcomes. The main outcomes measured include the number of clients screened for chronic pain and opioid misuse/OUD during the implementation and sustainment phases. The study also gathers data on treatment needs and evaluates the effectiveness of the provider-level intervention. Overall participation is structured around these phases and ongoing monitoring of implementation success.

CONDITIONS

Brief Title

Opioid and Pain Treatment in Indigenous Communities (OPTIC) Trial

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Willing and able to provide informed consent
  • Have English comprehension and proficiency
  • Receiving services at one of the participating study sites
  • Report current chronic pain and/or opioid misuse/opioid use disorder
  • Self-identify as American Indian or Alaska Native
Not Eligible

You will not qualify if you...

  • Having a psychiatric, cognitive, or medical condition that interferes with the consenting process

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Pre-Intervention

Duration - Approximately 6 months

Participants are observed at baseline prior to any involvement with the project.

Intervention

Duration - Approximately 6 months

Participants take part in a workgroup at their clinic to select specific goals to target during the implementation phase.

Implementation

Duration - Approximately 6 months

Participants experience evidence-based implementation strategies put into practice to improve screening and brief intervention for chronic pain and opioid misuse/OUD.

Sustainment

Duration - Approximately 6 months

Participants' clinics maintain the implementation phase goals and ongoing efforts are measured.

Trial Site Locations

Total: 3 locations

1

Clinic Site A (blinded pending tribal approval)

Arcata, California, United States, 95521

Actively Recruiting

2

Clinic Site C (blinded pending tribal approval)

Minneapolis, Minnesota, United States, 55404

Not Yet Recruiting

3

Clinic Site B (blinded pending tribal approval)

Toppenish, Washington, United States, 98948

Not Yet Recruiting

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Research Team

K

Kamilla L Venner, PhD

A

Angel R Vasquez, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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