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Search / Trial NCT05619497

The OPENS Trial: Offering Women PrEP (Aim 2)

Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · Nov 14, 2022

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Pre Exposure Prophylaxis (Pr Ep) Hiv Prevention Behaviors Hiv Prevention Methods Hiv Education African American, Latina, Women Of Color Shared Decision Making Shared Decision Making Decision Making, Shared Trauma Informed Care Trauma Informed Care Patient Decision Support Patient Decision Aid Public Health Clinic Health Department Clinic Southeastern U.S.

ClinConnect Summary

The OPENS Trial is a study aimed at improving access to HIV prevention methods, specifically for women, particularly women of color, in Duval County, Florida. This area has one of the highest rates of HIV infections among women in the U.S. The trial is investigating new ways to help women learn about HIV risks and prevention options through a decision support tool that can be used on a tablet. The study also includes training for clinic staff to ensure they provide supportive and understanding care when discussing HIV prevention. Participants will take part in two phases: first, they will receive care at a trained clinic without using the tablet tool, and then they will use the tool before their visit to help them make informed decisions.

To participate, women aged 18 to 45 who speak English and are not living with HIV can join the study. It's important that they are interested in learning about HIV prevention options. Participants will share their experiences with HIV prevention counseling and their thoughts on using prevention methods like PrEP (a medication that helps prevent HIV). The study will also follow up with participants three months later to see if they started using any HIV prevention methods. This trial aims to provide valuable insights into how to better support women in making informed choices about their health.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Self-identify as a woman (regardless of pregnancy status)
  • Age 18 years - 45 years
  • Not known to be living with HIV (based on self-report)
  • English speaking
  • Interested in participating in the study
  • Exclusion Criteria:
  • Unable to consent
  • Currently using PrEP
  • Those who were assigned male at birth and self-identify as a man
  • Unwilling to be contacted in 3 months

About University Of California, San Francisco

The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.

Locations

Jacksonville, Florida, United States

Patients applied

0 patients applied

Trial Officials

Christine Dehlendorf, MD, MAS

Principal Investigator

University of California, San Francisco

Akilah Pope, MD

Principal Investigator

Florida Department of Health, Duval County

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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