跳至主要内容
临床试验/NCT03685045
NCT03685045招募中不适用

Enhancing Treatment of Hepatitis C in Opioid Substitution Settings II (ETHOS II): A Partnership Project to Enhance Hepatitis C Care in Drug and Alcohol Clinics

Kirby Institute61 个研究点 分布在 1 个国家目标入组 6,000 人开始时间: 2018年5月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
6,000
试验地点
61
主要终点
Number of participants commencing anti-HCV treatment

研究概览

简要总结

The overall goals of the ETHOS II Project are to enhance hepatitis C virus (HCV) care in drug treatment clinics and needle and syringe programs (NSPs) in New South Wales and Australia, and to develop a translational framework for subsequent establishment of HCV screening and treatment programs in drug treatment clinics and NSPs across NSW and nationally.

详细描述

The ETHOS II Project is a collaborative research project led by the Kirby Institute, UNSW Sydney, in partnership with:

  • The Centre for Social Research in Health, UNSW Sydney
  • NSW Health
  • NSW Users and AIDS Association
  • Hepatitis NSW
  • Australasian Society for HIV, Viral Hepatitis and Sexual Health Medicine (ASHM)

The overall goals of the ETHOS II Project are to enhance hepatitis C virus (HCV) care in drug treatment clinics and needle and syringe programs (NSPs) in New South Wales and Australia, and to develop a translational framework for subsequent establishment of HCV screening and treatment programs in drug treatment clinics and NSPs across NSW and nationally.

The ETHOS II Project is divided into three parts:

I. ETHOS ENGAGE cohort; II. Qualitative research on barriers/facilitators to HCV care; III. HCV toolkit, education and training.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
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

  • Participant has voluntarily signed the informed consent form;
  • 18 years of age or older;
  • History of injecting drug use*;
  • Recent injecting drug use (previous six months) or currently receiving OST*.
  • These criteria will not apply for recruitment from residential rehabilitation centres

排除标准

  • 未提供

研究组 & 干预措施

Campaign Days

Experimental

All participants have the intervention of the campaign days which include hepatitis C screening, fibroscans and clinical assessments.

干预措施: Campaign days (Procedure)

结局指标

主要结局

Number of participants commencing anti-HCV treatment

时间窗: Every year post enrolment for up to 3 years

Evaluation of number of participants commencing anti-HCV treatment

次要结局

未报告次要终点

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (61)

Loading locations...

相似试验