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临床试验/NCT06487390
NCT06487390
已完成
不适用

PrEP Pro: Adapting a Multi-component Intervention to Train and Support Providers to Promote PrEP for Adolescent Girls and Young Women in the Deep South

University of Alabama at Birmingham1 个研究点 分布在 1 个国家目标入组 46 人2023年4月21日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
HIV Infections
发起方
University of Alabama at Birmingham
入组人数
46
试验地点
1
主要终点
Feasibility of Intervention Implementation
状态
已完成
最后更新
4个月前

概览

简要总结

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.

注册库
clinicaltrials.gov
开始日期
2023年4月21日
结束日期
2024年9月15日
最后更新
4个月前
研究类型
Interventional
研究设计
Single Group
性别
All

研究者

责任方
Principal Investigator
主要研究者

Lynn T. Matthews

Associate Professor of Medicine

University of Alabama at Birmingham

入排标准

入选标准

  • 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

排除标准

  • (a) unable or unwilling to provide informed consent

结局指标

主要结局

Feasibility of Intervention Implementation

时间窗: 6 months

Feasibility of Intervention: 4 items, 5-point Likert scale, scale values range from 1-5 with higher score meaning more feasible to implement

Acceptability

时间窗: 6 months

Acceptability of Intervention: 4 items, 5-point Likert scale, scale values range from 1-5 with higher score meaning the intervention is more acceptable to participants

次要结局

  • HIV Epidemiology Knowledge Assessment(6 months)
  • Sexual History Taking Practices(6 months)
  • PrEP Knowledge, Willingness to Prescribe, Prescribing Practices(6 months)
  • STI Screening Practices(6 months)
  • HIV Screening Practices(6 months)

研究点 (1)

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