๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-06-26

Telehealth vs In-Person Evaluation of Addiction Treatment After Visiting the Emergency Department (NCT06961058)

In Person vs Telehealth Opioid Use Disorder Treatment After Patients Leave the Emergency Department

๐ŸŸข Recruiting Observational / Diagnostic ๐Ÿ“‹ Clinical Research Protocol Sponsor: University of California, Davis

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

Main study objective: compare long-term buprenorphine treatment outcomes for patients who start buprenorphine for opioid use disorder (OUD) in the emergency department and are then referred to get outpatient buprenorphine treatment either via telehealth or at an in-person clinic. Researchers will: Compare rates of establishing outpatient OUD treatment, how long patients stay on buprenorphine, and patients' experience with care to determine whether patient experiences and outcomes are better for patients referred to telehealth treatment versus patients patients referred to in-person treatment after they leave the emergency department. Participants will: Be recruited from 3 different hospital emergency departments. Answer questionnaires at baseline and then 1, 3, 6, and 9 months after their initial emergency department visit.

Who can join: Review the eligibility criteria below.

Location: El Centro Regional Medical Center Emergency Department โ€” El Centro, California

Age range: 18 Years

๐Ÿงช Interventions in This Study

  • referral to telehealth treatment (OTHER)
  • referral to in person treatment (OTHER)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (3 Sites)

  • El Centro Regional Medical Center Emergency Department โ€” El Centro, California
  • University of California Davis Emergency Department โ€” Sacramento, California
  • Olive View - UCLA Medical Center Emegency Department โ€” Sylmar, California

๐Ÿ“ž Contact the Study Coordinator

Phone: (916) 734-7391

Email: masoulsby@health.ucdavis.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—