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临床试验/NCT05520905
NCT05520905招募中不适用

Evaluation of the Feasibility, Acceptability, and Effectiveness of TelePrEP for At-risk Youth in Colorado

University of Colorado, Denver1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2023年4月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
100
试验地点
1
主要终点
Retention

研究概览

简要总结

Youth represent the largest proportion of new HIV infections in Colorado, reflective of their inadequate access and uptake of pre-exposure prophylaxis(PrEP)for HIV prevention. Colorado's 2019 HIV/AIDS Prevention Program state-wide review of PrEP barriers showed PrEP eligible individuals do not access PrEP services due to lack of interest, not wanting referral to a navigator, and low estimation of HIV risk. The overall goal is to provide youth at higher risk for HIV with an effective youth informed telemedicine delivery of PrEP (TelePrEP) that addresses PrEP barriers and contributes to ending the HIV epidemic in Colorado. The primary objective will be proportion of youth retained on PrEP 12 months after initiation. The hypotheses are that a TelePrEP model for youth will be acceptable and feasible and will result in successful initiation, persistence and retention on oral PrEP.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
14 Years 至 24 Years(Child, Adult)
性别
Male
接受健康志愿者
是

入选标准

  • •HIV negative
  • •Eligible for PrEP using emtricitabine (F)/tenofovir alafenamide (TAF) (F/TAF) (brand name Descovy) based on current CDC guidance
  • •assigned male at birth
  • •has had male sex partners in the past 6 months (and not in a monogamous partnership with a recently tested, HIV-negative man) and
  • •either any sex without a condom in the past 6 months or
  • •a bacterial sexually transmitted infection
  • •Consents to TelePrEPvisits
  • •Willing to use current insurance coverage for clinic and laboratory services OR willing to be assisted to obtain insurance coverage OR eligible for other coverage such as Title X funds or charity care

排除标准

  • •HIV-infection or concern for acute HIV infection until ruled out
  • •Pregnancy
  • •Persons at risk through receptive vaginal sex including cisgender women and transgender men (persons assigned female sex at birth)
  • •Persons with only injection drug indications for PrEP without sexual risk indications outlined in inclusion criteria

研究组 & 干预措施

Telemedicine for pre-exposure prophylaxis of HIV

Experimental
  1. We will identify youth potentially eligibile for PrEP using tenfovir alefenamide/emtricitabine (TAF/FTC).
  2. Eligible youth will be contacted for rapid (same day) consenting and enrollment.
  3. Participants who consent to the study will undergo a PrEP initiation visit either the same day or within two weeks with a provider. The initial visit may be in-person or via Telemedicine.
  4. TelePrEP visits may be carried out in the setting of the participant's choosing and may include home or at a community organization.
  5. Recommended laboratory testing will be arranged as part of the PrEP initiation visit. HIV testing will be carried out as well as Centers for Disease Control and Prevention (CDC)-recommended laboratory testing will be obtained.
  6. TelePrEP(or in-person visits as needed) will be conducted by a skilled multidisciplinary team one month after initiation and then every three months.

干预措施: TelePrEP (Other)

结局指标

主要结局

Retention

时间窗: 48 weeks

Retention on PrEP at week 48. Retention in PrEP care 12 months after initiation as defined by either PrEP clinic visit (telehealth or in-person) or prescription refill.

次要结局

  • TelePrEP Feasibility(48 weeks)
  • TelePrEP Acceptability(48 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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TelePrEP for At-risk Youth in Colorado | 临床试验