Start the Conversation: Evaluating Implementation of a Multi-level PrEP Initiative for Black Cisgender Women in Nola

NCT05909176 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2025-07-23

No results posted yet for this study

Summary

The study objectives are to:

* Evaluate implementation outcomes from piloting the Start the Conversation Initiative
* Assess initial indicators of clinical effectiveness among patients engaged in the Start the Conversation Initiative

These outcomes will be assessed qualitatively through in-depth interviews (IDIs), debriefing sessions with GYN residents and leadership, medical chart reviews and/or de-identified Epic queries, training records, discussions with the Black Women and PrEP (BWAP) Task Force, and social media metrics.

Conditions

  • Preexposure Prophylaxis
  • HIV Infections

Interventions

BEHAVIORAL

GYN Residency Training

The combined care model will be implemented and during months 5-14.

BEHAVIORAL

Social Media Campaign

The social media campaign will be implemented along with the combined care model in months 15-18.

Sponsors & Collaborators

  • Louisiana State University Health Sciences Center in New Orleans

    collaborator OTHER
  • National Institute of Mental Health (NIMH)

    collaborator NIH
  • Duke University

    lead OTHER

Principal Investigators

  • Amy Corneli, MPH, PhD · Duke University

  • Meredith Clement, MD · Louisiana State University Health Sciences Center

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-05-30
Primary Completion
2024-10-31
Completion
2025-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05909176 on ClinicalTrials.gov