跳至主要内容
临床试验/NCT06335121
NCT06335121尚未招募不适用

Implementation of PrEP Care Among Women in Family Planning Clinics

Rush University Medical Center0 个研究点目标入组 250 人开始时间: 2026年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
250
主要终点
PrEP prescriptions among Black women accessing PPIL services and eligible for PrEP.

研究概览

简要总结

This study will evaluate implementation strategies to address barriers and increase uptake of PrEP among Black cisgender women in Planned Parenthood of Illinois (PPIL) health centers.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Eligible participants include ciswomen presenting at a PPIL health center with a positive STI test (syphilis, gonorrhea, or chlamydia) and identified in the EHR using STI testing records and new fields for optimizing support of provider PrEP counseling.

排除标准

  • - Participants will be excluded if they are not PrEP eligible, have a negative STI test, or are not identified in the EHR.

结局指标

主要结局

PrEP prescriptions among Black women accessing PPIL services and eligible for PrEP.

时间窗: 1 month

PrEP eligibility among Black women will be defined based on positive STI test and identified in the EHR using STI testing records and new fields for optimizing support of provider PrEP counseling. Using de-identified patient-level EHR data for eligible women at each clinic within each time point, we will create a dichotomous variable for having received a prescription for PrEP during a given time period.

次要结局

  • Receipt of PrEP refills among Black women accessing FP services at 6 months.(6 months)

研究者

申办方类型
Other
责任方
Sponsor

相似试验