Client-Centered Counseling During Routine/Opt-Out HIV-Testing in Uganda
研究概览
地位
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
-
-
-
Gombe、乌干达
- Gombe Hospital
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- at least 18 years of age,
- have come to the outpatient clinic for a medical concern (e.g., cough, malaria, but not those seeking voluntary HIV-counseling and testing,
- sexually active within the prior 3-months,
- not currently pregnant,
- no confirmed HIV-positive test result prior to the present HIV-test, and
- live not more than 30km from Gombe Hospital in Uganda (to facilitate follow-up)
Exclusion Criteria:
- less than 18 years of age,
- having come to the clinic seeking voluntary HIV-counseling and testing,
- not sexually active in prior 3 months,
- currently pregnant,
- confirmed prior HIV positive test,
- live more than 30km from the hospital
学习计划
研究是如何设计的？
设计细节
- 主要用途：预防
- 分配：非随机化
- 介入模型：并行分配
- 屏蔽：单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的：Motivational interviewing counseling
The brief intervention is adapted from the OPTIONS project, which is a brief client-centered risk reduction intervention for HIV-positive patients in clinical care. The OPTIONS intervention content is based upon the IMB model of health behavior change, and uses motivational interviewing techniques to create client-centered discussions in which HIV counselors and patients collaborate to identify patients' HIV transmission risk behaviors and to mutually identify strategies and goals for reducing the patient's risky behavior. The brief intervention will be facilitated by health care providers (nurses, lab technicians) specifically trained in the intervention protocol and will consist of 2 brief counseling sessions occurring during the same-day rapid HIV-testing procedure |
|
|
有源比较器：Standard of care counseling
Participants in this study condition will receive standard-of-care counseling that is usually implemented during HIV testing.
|
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Sexual risk behavior
大体时间：6 months
|
Unprotected sex with serodiscordant or unknown HIV status partners
|
6 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Uptake of partner testing
大体时间：6 months
|
Partner uptake of HIV testing
|
6 months
|
合作者和调查者
调查人员
- 首席研究员：Susan M Kiene, PhD、UConn Health
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- SK_UG_K01
- K01MH083536 (美国 NIH 拨款/合同)
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.