跳至主要内容
临床试验/NCT05794646
NCT05794646进行中(未招募)不适用

Community Intervention to Eliminate HCV Among People Who Use Drugs. Implementation Study in the Cities of Paris, Marseille, Lyon and Fort-de-France, France.

ANRS, Emerging Infectious Diseases7 个研究点 分布在 2 个国家目标入组 3,400 人开始时间: 2023年10月2日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
3,400
试验地点
7
主要终点
Acceptability and relevance of the RDS and implementation strategy : a qualitative study

研究概览

简要总结

The goal of this interventional study is twofold with the evaluation of the feasibility and potential usefulness of an implementation strategy, and the efficiency of a community-based model of mass screening and immediate treatment of hepatitis C among People Who Use Drugs (PWUD) in three major cities in mainland France (Paris, Lyon and Marseille) and in one overseas city (Fort-de-France). The investigators will also describe the psychological and infectious comorbidities of drug users, determine the stages of the HCV (Hepatitis C Virus), HBV (Hepatitis B Virus), HIV (Human Immunodeficiency Virus) care cascade, and analyze the factors associated with HCV treatment failure. A qualitative study will investigate the acceptability of the RDS model.

Participants will be screened in an out of bound research center and receive appropriate treatment for infectious, addictological and psychiatric troubles. They will receive coupons to give to their peers for them to participate in the study.

Researchers will also compare the acceptability of referral to psychiatric care directly at the research site (intervention group) with that of referral directly to a city facility (control group).

详细描述

Current state of knowledge:

In France, the prevalence of chronic hepatitis C in the general population was 0.3% in 2015. However, this prevalence is much higher in certain population subgroups. Thus PWUD are a population at risk of HCV infection (risky behaviors, sharing injection equipment).

In order to achieve the goal of eliminating hepatitis C by 2025 in France, three types of actions must be taken: developing off-premises screening strategies, improving access to treatment, and improving prevention. These actions correspond to micro-elimination practices.

Although there are many possible sites of care for PWUD, many PWUD do not attend the prevention and care system.

Despite the advent of new direct antiviral agents (DAAs) that cure infection in more than 95% of cases and the indication to treat all PWUDs, access to HCV treatment in this at-risk group remains low. Better control of HCV infection in high-risk groups such as PWUD would, beyond the individual benefit, greatly reduce the dynamics of the epidemic.

研究设计

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

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Acceptability and relevance of the RDS and implementation strategy : a qualitative study

时间窗: From before the RDS implementation until the end of the study, up to 2 years

The investigators will use a socio-anthropological method to target the PWUD participating in the RDS as well as the workers in the places where the RDS will have started. In each study city, 15 semi-structured interviews will be conducted with PWUD who participated in the RDS. Participants who are not followed up in outreach structures will be over-represented to delve deeper into the pathways of these individuals. Two focus groups in each city will be carried-out (one before the implementation of the RDS and one at the end of the study), in order to collect their feelings on the use and relevance of the toolkit for the implementation of the RDS. The interviews and focus groups will be conducted using an interview grid that will be constructed to meet the objectives of the study. This grid will guide the investigators around different main themes: people's backgrounds, role of the facilitators, perception of RDS (understanding, acceptability, strengths and weaknesses).

Percentage of HCV cured PWUD participants (SVR12) among those with a positive HCV viral load at baseline

时间窗: 12 weeks after the end of the 2 to 3 months HCV treatment

Number of HCV cured PWUD participants, defined as SVR12, i.e. undetectable HCV RNA viral load in a veinous sample measured by quantitative PCR (polymerase chain reaction) 12 weeks after the end of the antiviral treatment; divided by the number of participants with a positive HCV viral load in a veinous sample at baseline.

次要结局

  • Number of PWUD in the arrondissements of Paris (neighborhoods involved in seed distribution), and the cities of Lyon, Marseille and Fort-de-France(At the end of the RDS)
  • HCV treatment failure defined as detectable viral load 12 weeks after HCV treatment completion(12 weeks after the end of the 2 to 3 months HCV treatment)
  • Proportion of participants with positive HCV RNA among all participants(At baseline)
  • Assessment of HCV cascade of care at inclusion : participants with a positive HCV RDT(At baseline)
  • Assessment of HCV cascade of care at inclusion : participants with known HCV status(At baseline)
  • Proportion of participants with detectable HBsAg(At baseline)
  • Proportion of participants in Fort-de-France with a positive test for syphilis(At baseline)
  • Assessment of HCV cascade of care at inclusion : participants who were treated for HCV(At baseline)
  • Assessment of HCV cascade of care at inclusion : participants with known chronic hepatitis C status and undetectable HCV RNA(At baseline)
  • Cost of the intervention per screened participant(Through study completion, an expected time frame of 2 years)
  • Cost of the intervention per participant cured of hepatitis C(Through study completion, an expected time frame of 2 years)
  • HIV care cascade assessment at inclusion : HIV-positive participants on antiretroviral therapy(At baseline)
  • Proportion of participants with a positive HIV RDT among participants(At baseline)
  • HIV care cascade assessment at inclusion : participants with known HIV status(At baseline)
  • HIV care cascade assessment at inclusion : participants on effective antiretroviral therapy(At baseline)
  • Proportion of participants in Fort-de-France with a positive PCR for gonorrhea(At baseline)
  • Proportion of participants in Fort-de-France with a positive PCR for chlamydia(At baseline)
  • Success of psychiatric referral at 6 months(At 6 months)
  • Prevalence of psychological pathologies(At baseline)
  • Success of infectious diseases referral(At 6 months)
  • Success of addictological referral(At 6 months)
  • Success of psychiatric referral at 3 months(At 3 months)

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (7)

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