THRIVE: Culturally AdapTed Harm Reduction Intervention

Description

The goal of this study is to develop and test a culturally adapted harm reduction intervention among Black adults who misuse opioids and/or stimulants. The questions it aims to answer include: will the culturally adapted harm reduction educational intervention increase overall knowledge of overdose and prevention/intervention techniques and increase confidence and willingness to use/teach interventions to others at-risk.

Conditions

Opioid Use, Stimulant Use

Study Overview

Study Details

Study overview

The goal of this study is to develop and test a culturally adapted harm reduction intervention among Black adults who misuse opioids and/or stimulants. The questions it aims to answer include: will the culturally adapted harm reduction educational intervention increase overall knowledge of overdose and prevention/intervention techniques and increase confidence and willingness to use/teach interventions to others at-risk.

Culturally AdapTed Harm Reduction Intervention: Community Engaged InterVention for Black Adults That MisusE Opioids and Stimulants

THRIVE: Culturally AdapTed Harm Reduction Intervention

Condition
Opioid Use
Intervention / Treatment

-

Contacts and Locations

Louisville

Louisville Central Community Center, Louisville, Kentucky, United States, 40203

Cincinnati

Urban Minority Alcoholism and Drug Abuse Outreach Program (UMADAOP) of Cincinnati, Cincinnati, Ohio, United States, 45219

Cincinnati

University of Cincinnati, Cincinnati, Ohio, United States, 45221

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Identify as Black or African American
  • * Currently a resident of study areas
  • * Report misuse of stimulants and/or opioids in the last six months
  • * Do not identify as Black or African American
  • * If they participated in Aim 1 of the study
  • * Do not want to be audio-recorded

Ages Eligible for Study

18 Years to 65 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Brittany Miller-Roenigk,

Brittany Miller-Roenigk, PhD, PRINCIPAL_INVESTIGATOR, University of Kentucky

Study Record Dates

2025-06