N/A
Completed N=46
Multi-component Intervention to Train Providers to Promote PrEP for Girls and Women in the Deep South
Source: ClinicalTrials.gov NCT06487390 ↗Enrolled (actual)
46
Serious AEs
0.0%
Results posted
Dec 2025
Primary outcomePrimary: Feasibility of Intervention Implementation — 4.28 Scores on a scale
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.
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 | — |
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
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. Informational only — not medical advice.