跳至主要内容
临床试验/NCT01419899
NCT01419899已完成2 期

Phase 2/3 Clinical Trial of the Effect of a Brief Intervention on Uptake of Rapid Testing for HIV and Hepatitis C Among Emergency Department Patients

Rhode Island Hospital2 个研究点 分布在 1 个国家目标入组 398 人开始时间: 2011年1月最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
398
试验地点
2
主要终点
The agreement of the participant to be tested for HIV and hepatitis C

研究概览

简要总结

The purpose of this study is to determine if a brief intervention delivered to emergency department patients increases the uptake of rapid HIV and hepatitis C testing in comparison to no brief intervention.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Emergency department patient.
  • Does not know HIV or hepatitis C status.
  • Has an ASSIST V3 score that indicates recent illicit and/or prescription drug use.
  • Fluency in English or Spanish.

排除标准

  • Critically ill or injured.
  • Homicidal and/or suicidal intention.
  • Age < 18 years or > 64 years.
  • Does not speak English or Spanish.

研究组 & 干预措施

Standard Care

No Intervention

This arm of the study will receive an assessments survey. Following the assessment the participants will be offered free rapid testing for HIV and hepatitis C.

Brief Intervention

Experimental

This arm of the study will receive an assessments survey followed by a brief intervention concerning the relationship between the participants use of drugs and/or sexual risk and rik for HIV and hepatitis C infections. Following the intervention the participants will be offered free rapid testing for HIV and hepatitis C.

干预措施: Brief motivational intervention (Behavioral)

结局指标

主要结局

The agreement of the participant to be tested for HIV and hepatitis C

时间窗: Within four hours of being consented into the study

We will measure the acceptance of free rapid testing for HIV and hepatitis C among the intervention and control groups

次要结局

  • Identifying risky sexual behaviors of study participants(Within four hours of being consented into the study)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Roland C. Merchant, MD. MPH, ScD

Associate Professor

Rhode Island Hospital

研究点 (2)

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