N/A N=46 Other

Multi-component Intervention to Train Providers to Promote PrEP for Girls and Women in the Deep South

HIV Infections · Sexually Transmitted Diseases

Bottom Line

View on ClinicalTrials.gov: NCT06487390 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Dec 2025

Primary outcome: Primary: Feasibility of Intervention Implementation — 4.28 Scores on a scale

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: PrEP Pro training intervention (Behavioral)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: University of Alabama at Birmingham
Primary completion: Sep 2024

Outcome Measures

Outcome	Result	p-value
PRIMARY Feasibility of Intervention Implementation	4.28	—
PRIMARY Acceptability	4.31	—
SECONDARY HIV Epidemiology Knowledge Assessment	18.75	—
SECONDARY Sexual History Taking Practices	2.5; 3.0; 3; 2.7	—
SECONDARY PrEP Knowledge, Willingness to Prescribe, Prescribing Practices	16; 26; 6	—
SECONDARY STI Screening Practices	90.63; 56.25; 71.88; 34.38	—
SECONDARY HIV Screening Practices	40.63; 28.13	—

Summary

The goal of this study is to adapt evidence-based curriculum on HIV epidemiology and PrEP prescription to train family medicine physician trainees to take a thorough sexual history and discuss HIV/STI prevention and PrEP options with adolescent patients in Alabama. The primary outcomes of the study are: * Feasibility of the PrEP Pro training intervention * Acceptability of the PrEP Pro training intervention Secondary outcomes include: * Behavioral changes in sexual history taking performed by physician trainees * PrEP knowledge and prescribing practices * HIV and STI screening practices Participants will receive training on sexual history taking and HIV prevention options, including PrEP prescription and management. They will complete a pre-training survey (enrollment) and post-training survey (6 months post enrollment) to understand differences in knowledge and practice before and after receiving the training intervention. The post training survey will also assess acceptability and feasibility of the intervention. A subset of participants will complete qualitative in-depth interviews to further discuss their experiences with the program and suggestions for future adaptations.

Eligibility Criteria

Inclusion Criteria

licensed HCP (MD, DO) trainee
providing medical care to AGYW in AL
working in a clinic setting where at least 20% of the population is Black
able/willing to provide informed consent

Exclusion Criteria

(a) unable or unwilling to provide informed consent

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT06487390). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.