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Recruiting

NCT Number: NCT04811014

Young Houston Emergency Opioid Engagement System

The Houston Emergency Response Opioid Engagement System for Youths and Adolescents (Young HEROES) is a community-based research program integrating assertive outreach, medication for opioid use disorder (MOUD), behavioral counseling, and peer recovery support. The objective is to compare differences in engagement and retention in treatment for individuals with opioid use disorder. The investigators also intend to understand the prevalence of opioid overdoses and OUD among youth in Houston.

Recruiting

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Key information

Age range

13 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

The University of Texas Health Science Center at Houston

Houston, Texas, 77030, United States

Location status: Recruiting

Location contact

James R Langabeer, PhD

CONTACT

[email protected]

713-500-3925

About this study

The Houston Emergency Response Opioid Engagement System for Youths and Adolescents (Young HEROES) is a non-randomized cohort study based at the University of Texas Health Science Center of Houston. This study recruits participants through three avenues: assertive community outreach with a peer coach and paramedic following and opioid overdose, community referrals, and emergency department referrals. The study explores the effect of the combination of assertive outreach, same-day induction into medication for opioid use disorder, ongoing maintenance treatment, behavioral counseling, peer recovery support, and paramedic follow-up on patient outcomes. The primary outcome is engagement and retention in outpatient treatment. Secondary outcomes include quality of life assessment as well as subsequent relapses and overdoses. The hypothesis is that patients with earlier induction into MOUD treatment who receive routine follow-up, are more likely to engage and remain in treatment long-term.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Buprenorphine, Naloxone Drug Combination

Drug

8mg of buprenorphine/2mg of naloxone to initiate MOUD treatment and bridge, if necessary, until referral to MOUD clinic can be made for ongoing treatment

Other names: Suboxone

Individual counseling

Behavioral

One-on-one counseling with a licensed chemical dependency counselor

Other names: Therapy

Peer Recovery Support Services

Behavioral

24/7 support from our team of certified peer recovery support specialists to assist with emotional support and case management

Other names: Peer Coaching, Recovery Coaching

Support group

Behavioral

Referrals to youth-focused support groups and eventual creation of in-house youth-focused support groups

Other names: Group Therapy

Referral to Medication Management

Behavioral

Study staff will refer patients to long-term MOUD providers in the community

Assertive Outreach

Behavioral

The investigators will conduct weekly outreach to youths who experienced an opioid overdose and attempt to initiate treatment. Outreach is completed by a paramedic and peer coach.

Other names: Community Outreach

Primary outcomes

  1. Patient retention in treatment

    Time frame: 30 days after enrollment

    Percentage of enrolled youth in treatment over time

  2. Patient abstinence from opioids

    Time frame: 30 days after enrollment

    Days without substance use

Secondary outcomes

  1. Frequency of opioid emergencies among adolescents in Houston, Texas

    Time frame: Through study completion, an average of 3 years

    Prevalence of opioid overdoses among youth

Study contacts

Contact information is provided by the study sponsor or research team.

James R Langabeer, PhD

CONTACT

[email protected]

713-500-3925

Meredith M O'Neal, MA

CONTACT

[email protected]

713-500-3624

Sponsors and collaborators

Lead sponsor

The University of Texas Health Science Center, Houston

Other

Registry information

Official study title

Houston Emergency Engagement System for Youths and Adolescents

Acronym: YHEROES

Important dates

Study start
2021
Primary completion
2030
Study completion
2030
First posted
Mar 23, 2021
Registry last updated
Oct 1, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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