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临床试验/NCT01197027
NCT01197027已完成3 期

Feasibility and Acceptability Study of an Individual-Level Behavioral Intervention for Individuals With Acute and Early HIV-Infection

HIV Prevention Trials Network1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2010年2月1日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
28
试验地点
1
主要终点
Proportion of participants in the experimental arm who receive the first four intervention sessions between enrollment and week 2 visit

研究概览

简要总结

The purpose of this study is to evaluate the acceptability and feasibility of an enhanced, individual-level counseling intervention for individuals in the acute and early phase of HIV infection aimed at reducing risk behaviors.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
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

  • Be enrolled in CHAVI 001 Note: The inclusion and

排除标准

  • for CHAVI 001 are provided below. The criteria will not be reassessed prior to enrollment in HPTN
  • Inclusion Criteria from CHAVI 001
  • Men and women aged ≥ 18 years at the time of screening.
  • Able and willing to provide adequate information for locator purposes.
  • Hemoglobin > 10.0 g/dL.
  • Willing to receive HIV test results.
  • Not intending to relocate out of the area for the duration of study participation and does not have a job or other obligations that may require long absences from the area.
  • Has acute HIV infection. (See Section 2.3 for definition).
  • Exclusion Criteria:
  • Any prior or current use of antiretroviral therapy (ART). This does not apply to individuals screening for Group 1A. ART use for the prevention of perinatal transmission may be waived after prior consultation with the protocol team.
  • Previous or current participation in a HIV vaccine study. HPTN 062 Version 3.0 Final 03 August 2010
  • Any condition that, in the opinion of the Investigator of Record, would make participation in the study unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.

结局指标

主要结局

Proportion of participants in the experimental arm who receive the first four intervention sessions between enrollment and week 2 visit

时间窗: Week 2

次要结局

  • Number of self-reported unprotected sex acts(6 months)

研究者

发起方
HIV Prevention Trials Network
申办方类型
Network
责任方
Sponsor

研究点 (1)

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