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临床试验/NCT06904820
NCT06904820招募中不适用

Acceptability and Feasibility of Simultaneous Screening for Viral Hepatitis B, C and HIV Among Drug Users and Vulnerable Populations, in Non-conventional Structures "Outside the Walls" by Dual Screening Method RTDs and FibroScan®

University Hospital, Limoges1 个研究点 分布在 1 个国家目标入组 2,300 人开始时间: 2025年6月5日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
2,300
试验地点
1
主要终点
Evaluate the acceptability and the feasibility of simultaneous screening for viral hepatitis B, C and HIV among drug users and vulnerable populations in non-conventional structures using a triple method with RTD and FibroScan® and GeneXpert®.

研究概览

简要总结

The "Scanvir" concept aims to achieve barriers to HCV screening and treating of marginalized patients. The concept is applicable to other various populations and territories and should effectively improve HCV patient's health outcomes. The main objective of the SCANVIR project was to evaluate the feasibility, acceptability and reproducibility of a "test, treat and cure" strategy for PWIDs and vulnerable populations during dedicated days in addiction care centers.

详细描述

According to the French recommendations, eliminating hepatitis C virus by 2025 could be a realistic public health goal in this country. A total of 71,466 patients had treatment initiation between 2015 and 2019. It is estimated that 100 000 people are still infected in 2019.

To meet these ambitious objectives, effective screening policies should be intensified and access to treatment promoted through new care strategies for patients who escape the usual care pathways i.e. people who inject drugs (PWIDs), prisoners, migrants and vulnerable populations.

PWIDs represent a large proportion of patients to be screened and treated. It's still not possible to accurately evaluate the number of drug users who are infected with HCV (45 000 people estimated).

Drug users sharing needles and syringes have poor access to treatment. Dealing with PWIDs in addiction care centers (CSAPA and CAARUD in France) is one way to promote HCV testing, and to keep them in the care pathway. This population requires dedicated models that reduce barriers to care: harm reductions policies, access to therapy in real time and follow-up for the detection of reinfection. So the investigator designed and applied a new innovative concept to test, treat and cure PWIDs in their own environment, called the SCANVIR program, initially tested in four French departments with a regional and now national extension.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Adult 18 and over
  • •Patient frequenting an unconventional structure "outside the walls" or referred by a professional in the care sector
  • •Patient not opposed to research

排除标准

  • •Age under 18
  • •Patient opposed to research

结局指标

主要结局

Evaluate the acceptability and the feasibility of simultaneous screening for viral hepatitis B, C and HIV among drug users and vulnerable populations in non-conventional structures using a triple method with RTD and FibroScan® and GeneXpert®.

时间窗: from enrollment to the end of the subject participation at the end of the day

Feasibility will be assessed by the number of days and the number of participants in all sessions. the acceptability of TROD and/or Fibroscan will be assessed by the number and proportion of double screenings (TROD and/or Fibroscan) performed in relation to the number of screenings offered

次要结局

  • Encourage HBV vaccination,(from enrollment to the end of the subject participation at the end of the day)
  • Reinforce screening for hepatitis B (HBV), hepatitis Delta (HDV) and HIV,(from enrollment to the end of the subject participation at the end of the day)
  • Offer rapid treatment to HCV-positive patients in precarious situations,(from enrollment to the end of the subject participation at the end of the day)
  • Reinforce education to prevent the risk of viral transmission,(from enrollment to the end of the subject participation at the end of the day)
  • Evaluate the feasibility of PCR (GeneXpert/Buvard),(from enrollment to the end of the subject participation at the end of the day)
  • Provide social support,(from enrollment to the end of the subject participation at the end of the day)
  • Assess associated co-morbidities: alcohol, cannabis, drug misuse, associated psychiatric pathologies,(from enrollment to the end of the subject participation at the end of the day)

研究者

发起方
University Hospital, Limoges
申办方类型
Other
责任方
Sponsor

研究点 (1)

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