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 — OTHEROverdose prevention resources (e.g., naloxone) are resources used to prevent drug overdose.
- Overdose prevention education — BEHAVIORALDeveloped 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 supportThis arm receives both overdose prevention education and access to overdose prevention resources.
- Experimental: Education onlyThe Education only arm receives overdose prevention education.
- Experimental: Access supportThis arm receives access to overdose prevention resources.
- No Intervention: ReferralThe 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
- Emma S Kay, PhD, MSW205-996-5547
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Alabama at Birmingham | Birmingham | Alabama | 35233 | - |
| University of Alabama at Birmingham | Birmingham | Alabama | 35233 | Emma S Kay, PhD (PRINCIPAL_INVESTIGATOR) |