Remote Intervention to Prevent Overdose

Part of paid clinical trials in Birmingham, Alabama.

Sponsor
University of Alabama at Birmingham
Study ID
NCT07128485
Status
Not Yet Recruiting

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Conditions

  • Accidental Overdose of Opiate

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Overdose prevention resources — OTHER
    Overdose prevention resources (e.g., naloxone) are resources used to prevent drug overdose.
  • Overdose prevention education — BEHAVIORAL
    Developed in the R61 phase, the educational intervention will provide participants with knowledge about how prevent drug overdose.

Study Details

This Type 1 hybrid effectiveness-implementation randomized controlled trial, A Remote Intervention to Prevent Overdose among People who Use Stimulants and/or Opioids, aims to address the United States opioid crisis driven by fentanyl and other synthetic opioids by reducing overdose rates. It is supported by and included in the HEAL Initiative. This study would be the first national, fully remote trial to assess the impact of remote education on overdose outcomes, using a novel 2x2 design crossing remote education with remote access support. This research will inform scalability around remote education programs to address the nation's opioid overdose crisis.

Key Dates

First listed
Aug 19, 2025
Start date
Jan 31, 2027
Status verified
Jun 2026
Primary completion
Nov 30, 2027
Completion
Nov 30, 2027

Study Design

Enrollment
100 participants (estimated)
Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION

Arms

  • Experimental: Education plus access support
    This arm receives both overdose prevention education and access to overdose prevention resources.
  • Experimental: Education only
    The Education only arm receives overdose prevention education.
  • Experimental: Access support
    This arm receives access to overdose prevention resources.
  • No Intervention: Referral
    The referral only arm receives a resource list for obtaining naloxone and other overdose prevention resources on their own.

Primary Outcome Measure

Overdose [ Time Frame: Baseline, 1 month, 3 months, 6 months ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
University of Alabama at BirminghamBirminghamAlabama35233-
University of Alabama at BirminghamBirminghamAlabama35233
Emma S Kay, PhD
205-996-5547
Emma S Kay, PhD (PRINCIPAL_INVESTIGATOR)

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