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临床试验/NCT04880200
NCT04880200已完成不适用

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 Washington3 个研究点 分布在 1 个国家目标入组 194 人开始时间: 2022年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
194
试验地点
3
主要终点
Time to viral suppression

研究概览

简要总结

This project (NCT04880200) 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

研究组 & 干预措施

POC NAT & Adherence Intervention

Experimental

These participants will receive the POC NAT test during their study visit. The result will be conveyed to their provider, who will deliver the result and an adherence intervention.

干预措施: POC NAT & Adherence Intervention (Diagnostic Test)

Standard of Care

No Intervention

These participants will receive the clinical standard of care during their visit.

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.

Achievement of Viral Suppression

时间窗: 1 year

Participants achieving an undetectable viral load during 1 year of follow up

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 (3)

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