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)
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
- 否
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
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
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
Joanne Stekler, MD MPH
Professor, School of Medicine
University of Washington
