Community-based program for youth with opioid use disorder
Official title: Houston Emergency Engagement System for Youths and Adolescents
Run by The University of Texas Health Science Center, Houston · NCT04811014 · Data updated 2026-11-12
This study is testing a community program that helps young people with opioid use disorder get better treatment and support to see if it keeps them engaged in recovery and reduces overdoses.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Ages | 13 Years to 17 Years |
| Sex | All |
| Enrollment | 250 (estimated) |
| Sponsor | The University of Texas Health Science Center, Houston Academic / other |
| Locations | 1 site (Houston, Texas) |
| Status | Recruiting |
| Started | April 19, 2021 |
| Main results expected | August 31, 2030 |
| Study ends | August 31, 2030 |
| Registry record updated | October 1, 2025 |
| Trial ID | NCT04811014 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are youths and adolescents who are opioid-dependent, willing to stop using opioids, and able to communicate in English.
✕Probably not a fit
Patients who are physiologically dependent on other substances requiring immediate medical attention or have severe medical conditions may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The Young Houston Emergency Opioid Engagement System (Young HEROES) is a community-based initiative aimed at improving treatment engagement for youths and adolescents with opioid use disorder. This non-randomized cohort study recruits participants through assertive outreach, community referrals, and emergency department referrals, providing immediate access to medication for opioid use disorder, behavioral counseling, and peer recovery support. The study evaluates the effectiveness of these combined interventions on patient outcomes, focusing on engagement and retention in treatment, as well as the prevalence of opioid overdoses among youth in Houston.
Why it matters
Potential benefit: If successful, this program could significantly improve treatment retention and reduce opioid-related overdoses among youth.
How similar studies have gone: Other studies have shown success with similar community-based approaches to opioid treatment, indicating potential for positive outcomes.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * In otherwise good health based on physician assessment and medical history * Drug screen positive for opioids * Patients express a willingness to stop opioid use * Meet Diagnostic and Statistical Manual of Mental Disorders - Text Revision (DSM-IV-TR) criteria for opioid dependence * Patients must be able to speak English * Be agreeable to and capable of signing the informed consent and assent (parent or guardian must consent, minor must assent) Exclusion Criteria: * Non-English-speaking patients * Have a known sensitivity to buprenorphine or naloxone * Be physiologically dependent on alcohol, benzodiazepines, or other drugs of abuse that require immediate medical attention. Other substance use diagnoses are not exclusionary. * Have a medical condition that would, in the opinion of the study physician, make participation medically hazardous, including unstable cardiovascular disease, neurological deficits, trauma, acute hepatitis, stroke, and liver or renal disease) * Be acutely psychotic, severely depressed, and in need of inpatient treatment, or is an immediate suicide risk * Be a nursing or pregnant female
Where it's running
-
The University of Texas Health Science Center at Houston
Houston, Texas, United States Recruiting
Study contacts
- Principal investigator: James R Langabeer, PhD — The University of Texas Health Science Center, Houston
- Study coordinator: James R Langabeer, PhD
- Email: james.r.langabeer@uth.tmc.edu
- Phone: 713-500-3925
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Bundled telehealth, peer support, and buprenorphine after ED discharge to prevent opioid overdoses
This trial tests a bundled approach with telehealth, peer support, buprenorphine, and care linkage to see if it helps people who have overdosed and were discharged from the ED continue treatment and avoid repeat overdoses.
-
Brief alcohol-focused program tailored for people taking buprenorphine
This project will try a short, opioid-informed alcohol counseling program for adults on prescribed buprenorphine who drink alcohol to see if it reduces drinking and helps them stay in treatment.
-
Mild electrical brain stimulation (tDCS) with cognitive training to reduce cocaine cravings.
This trial will test whether brief sessions of mild electrical brain stimulation (tDCS) combined with cognitive reappraisal training can lower craving in adults receiving inpatient treatment for cocaine use disorder.
-
Impact of MOUD Policy Changes During the Pandemic on Opioid and Alcohol Use Disorders
This study tests how federal and state policy changes during the COVID-19 pandemic affected access to and use of medications for opioid use disorder among Veterans with opioid or alcohol use disorders.
-
Kratom and other substances safety in people with past opioid use
This study tests kratom at different doses against a placebo and oxycodone to see how people with a history of opioid use tolerate and respond to them.
-
Lemborexant for insomnia in adults with opioid use disorder on buprenorphine
This trial will see if taking lemborexant each night for 8 weeks improves sleep, mood, and impulsive behavior in adults with moderate opioid use disorder who are stable on buprenorphine.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.