REMOTE VS. IN-PERSON STUDY EVALUATION (RISE) ABOVE OPIOID OVERDOSE
State University of New York at Buffalo
Summary
The study will employ a randomized, parallel-group design with two-stage randomization. After an initial brief screen for basic eligibility, participants will be randomized (within site) to either Remote (R) or In-Person (IP) Intake Groups. During the Intake, detailed consent and eligibility assessment will be completed. Participants who are eligible at the Intake will be randomized (within site and Intake Group) to R or IP Treatment and Assessment Groups. Participants will be followed for 3 months.
Eligibility
- Age range
- 18–99 years
- Sex
- All
- Healthy volunteers
- Yes
INCLUSION CRITERIA: Common to all 3 RCTs: 1. age18+ years 2. stable mailing address (for mailing study packets if assigned to Remote Intake and/or Remote Treatment/Assessment) within accessible range (1.5 hours) of each study site (per self report) 3. able to read, speak \& verbally comprehend English 4. currently own an iOS- or Android-compatible smartphone 5. have a valid e-mail address that is checked regularly (at least once per day) or have regular access to text messages (to access follow-up assessments) Specific to RCT 3: e) Meet criteria for Opioid Use Disorder and/or Stimulant Use…
Interventions
- BehavioralOpioid Overdose Prevention Training
All participants receive a brief training video for the use of naloxone for opioid overdose prevention and a naloxone kit.
Location
- University of Oklahoma Health CampusOklahoma City, Oklahoma