Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Approximately 6 months
Participants are observed at baseline prior to any involvement with the project.
Duration - Approximately 6 months
Participants take part in a workgroup at their clinic to select specific goals to target during the implementation phase.
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.
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
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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