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临床试验/NCT00164398
NCT00164398已完成2 期

HIP: HIV Intervention for Providers

Centers for Disease Control and Prevention1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2004年6月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
50
试验地点
1
主要终点
Self-reported, unprotected (without condoms) anal or vaginal sex with HIV-negative and unknown-status persons.

研究概览

简要总结

The purpose is to encourage Provider participants to evaluate high risk HIV transmission behaviors and offer prevention messages to their HIV+ patients which will, in turn, reduce rates of unprotected anal and/or vaginal sex with partners of known HIV sero-negativity or unknown HIV serostatus. It is hypothesized that patients of providers participating in the HIP intervention will report higher reduction in sexual risk practices, when compared to the patients of the providers who were randomized into the control condition.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
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
是

入选标准

  • •Provider participants: (1) licensed MD, NP or PA on staff at the participating institution; (2) has a minimum panel of 5 HIV+ patients; (3) sees patients at least one-half day per week in the clinical setting; (4) is willing to participate in all intervention training sessions; and (5) is willing and able to provide full informed consent.
  • •HIV+ patient participants:(1) report at least 1 encounter of unprotected anal or vaginal sex with known HIV- or unknown serostatus partner in the preceding six months; (2) patient's Primary Provider is enrolled as a participant in the study; (3) age 18 years or older; and (4) willing and able to provide informed consent.

排除标准

  • 未提供

结局指标

主要结局

Self-reported, unprotected (without condoms) anal or vaginal sex with HIV-negative and unknown-status persons.

次要结局

未报告次要终点

研究者

发起方
Centers for Disease Control and Prevention
申办方类型
Fed
责任方
Sponsor

研究点 (1)

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