Leveraging Video Logs as a Bridge to Pre-exposure Prophylaxis (PrEP) With Tailored Messaging to Black Women and Their Healthcare Providers in Texas.

Trial statusNot yet recruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexFemale
Age18-99
SponsorThe University of Texas Medical Branch, Galveston

About this trial

The primary objective of this R34 proposal is to increase willingness for PrEP initiation and PrEP initiation among Black Women (BW) and increase willingness to prescribe/refer pre-exposure prophylaxis (PrEP) to CBW among healthcare providers (HCPs) in Houston/Harris County, a high priority Ending the HIV Epidemic (EHE) jurisdiction.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

be a woman

be 18 years of age

have been sexually active with a man within the past 6 months

be fluent in English

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Video-log (vlog) series with videos tailored to cisgender Black women or to healthcare providers

    Behavioral

    This intervention is a video-log (vlog) series based health communication intervention that will be disseminated through community health centers (CHCs) and social media to increase willingness for and use of PrEP among cisgender Black women and to increase willingness to prescribe and refer PrEP among healthcare providers.

Treatment groups

78 Participants
are divided into 2 treatment groups
Group A: InterventionExperimental treatment 1 intervention
Group B: Standard of CareNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Number of participants with increased willingness to access or use PrEP

To assess whether participation in Project ROLE versus usual care will increase the willingness of Black women to access and/or use PrEP

Time frame
baseline and day of enrollment and baseline, 1-month, 3-month, and 6-month
2

Number of healthcare providers increased willingness to prescribe and/or refer PrEP

To assess whether participation in Project ROLE versus usual care will increase the willingness of healthcare providers to prescribe and/or refer PrEP to Black women

Time frame
baseline and day of enrollment and baseline, 1-month, 3-month, and 6-month

Secondary outcomes

1

Number of Black Women started to use of PrEP

To assess whether Black women started to use PrEP.

Time frame
1- month, 3-months, and 6-months follow-up visits
2

Number of PrEP prescriptions or referrals by healthcare providers

Using the clinical notes of electronic clinical records at participating CHCs.

Time frame
1- month, 3-months, and 6-months follow-up visits
3

PrEP adherence among those who initiated PrEP

Assess, using a urine drug screen, whether Black women who initiated PrEP adhered to the PrEP regimen.

Time frame
3-months and 6-months follow-up visits

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

The University of Texas Medical Branch, Galveston

Lead sponsor

National Institute of Mental Health (NIMH)

Collaborator

This trial is not recruiting at the moment. You can still explore other options: