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NOT YET RECRUITING
NCT07875569
NA

Remote vs. In-Person Study Evaluation (RISE) Trials: RISE Above Opioid Overdose (Trial 3 of 3)

Sponsor: State University of New York at Buffalo

View on ClinicalTrials.gov

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.

Official title: REMOTE VS. IN-PERSON STUDY EVALUATION (RISE) ABOVE OPIOID OVERDOSE

Key Details

Gender

All

Age Range

18 Years - 99 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-11

Completion Date

2028-05

Last Updated

2026-10-15

Healthy Volunteers

Yes

Interventions

BEHAVIORAL

Opioid Overdose Prevention Training

All participants receive a brief training video for the use of naloxone for opioid overdose prevention and a naloxone kit.

Locations (1)

University of Oklahoma Health Campus

Oklahoma City, Oklahoma, United States