Five Point Initiative: A Bundled Implementation Strategy to Address the HIV Epidemic in Black Communities

Description

The purpose of this study is to assess the effectiveness of the FPI bundled implementation strategy in increasing HIV testing, Pre-exposure prophylaxis (PrEP) linkage (e.g., prescription) and knowledge, and condom use/access.

Conditions

Hiv

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Study Overview

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Study Details

Study overview

The purpose of this study is to assess the effectiveness of the FPI bundled implementation strategy in increasing HIV testing, Pre-exposure prophylaxis (PrEP) linkage (e.g., prescription) and knowledge, and condom use/access.

Five Point Initiative: A Cluster Randomized Trial of a Bundled Implementation Strategy to Address the HIV Epidemic in Black Communities

Five Point Initiative: A Bundled Implementation Strategy to Address the HIV Epidemic in Black Communities

Condition
Hiv
Intervention / Treatment

-

Contacts and Locations

Miami

University of Miami, Miami, Florida, United States, 33136

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

  • * Any individual present during the community events at the "five points" (barbershop, hair/beauty salon store or salon, corner store/grocery/neighborhood restaurant, laundromats, car service provider \[e.g. gas station, mechanic, car wash\]) in predominantly Black communities in Miami where HIV prevalence is high.
  • * Pre- and Post-assessment: Individuals are only eligible to complete the survey one time during the Pre-Intervention and during the Post-Intervention phases.
  • * Intervention: Individuals are only eligible to participate in the Intervention phase of this study once every 6 months.
  • * Individuals who are unable to completely and fully understand the informed (verbal) consent process and the study procedures.
  • * Individuals who have previously completed the survey during the Pre-Intervention and Post-Intervention phases.
  • * Individuals who have participated in the Intervention phase of this study within less than 6 months.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

University of Miami,

Sannisha Dale, PhD, PRINCIPAL_INVESTIGATOR, University of Miami

Study Record Dates

2029-06-30