跳至主要内容
临床试验/NCT04880200
NCT04880200招募中不适用

The GAIN (Greater Access and Impact With NAT) Study: Improving HIV Diagnosis, Linkage to Care, and Prevention Services With HIV Point-of-Care Nucleic Acid Tests (NATs)

University of Washington2 个研究点 分布在 1 个国家目标入组 932 人开始时间: 2022年1月3日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
932
试验地点
2
主要终点
Time to viral suppression

研究概览

简要总结

This project will develop, implement, and evaluate models for use of point-of-care nucleic acid testing (POC NAT) among HIV-negative persons seeking HIV testing, PEP, and PrEP and HIV-positive persons in community and clinical settings. Study aims #1 and #2 will evaluate the sensitivity and specificity of a qualitative POC NAT in persons not known to be HIV-positive and will determine the impact of its use on PrEP uptake and persistence among persons testing HIV-negative and on time to HIV continuum of care outcomes among persons testing HIV-positive. Aim #3 will implement a POC NAT-tailored behavioral intervention to evaluate impact on time to virologic suppression among PLWH receiving ART. Aim #4 will quantify the acceptability and feasibility of implementation of POC NAT in community and clinical settings and collect cost and related data for cost-effectiveness analyses. Finally, in Aim #5, a distinct but related study will compare the sensitivity, specificity, and agreement of multiple POC NATs over a range of HIV RNA levels.

研究设计

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

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Persons who are HIV-positive and seeking care at Madison Clinic.
  • 18 years of age or older
  • Patient's provider is willing to deliver adherence intervention
  • Patient is getting a laboratory RNA viral load test that day.
  • Able to read and speak English

排除标准

  • Patients of unknown HIV status
  • Patients who have participated in the study before

结局指标

主要结局

Time to viral suppression

时间窗: Participants will be enrolled for up to 6 months

We will compare time to virologic suppression among participants randomized to the two arms.

次要结局

  • Participation(Participants will be enrolled for up to 6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Joanne Stekler, MD MPH

Professor, School of Medicine

University of Washington

研究点 (2)

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