Community Intervention to Eliminate HCV Among People Who Use Drugs. (ICONE2)

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

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).

Study Overview

• Status: Active, not recruiting
• Conditions: Substance Use Disorders; HCV
• Intervention / Treatment: Other: Hybrid effectiveness-implementation study type 2

Detailed Description

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.

The prevalence of psychiatric disorders in the PWUD population, especially the most precarious, is high, with at least one characterized psychiatric disorder observed in 50% to 80% of situations. The existence of unrecognized and untreated psychiatric disorders in these subjects is a factor of lesser access to somatic care, in particular to HCV care. Therefore, optimizing access to HCV care in the PWUD population requires the identification and appropriate management of psychiatric pathologies in these individuals.

Research Hypothesis:

The investigators hypothesize that the Respondent Driven Sampling (RDS) recruitment technique and the community-based approach can be implemented in large urban areas and legally allow for psychiatric support, often necessary in this vulnerable population.

This study will also make it possible to estimate the size of the different populations of drug users in 4 large cities in France, one of which is overseas, in which the local specificities in terms of drug use but also of comorbidities will have to be studied (Capture/recapture).

In addition, the use of this recruitment technique coupled with the involvement of peers, will make it possible to define the different drug uses in the user population in the major cities of metropolitan France and in Fort-de-France. This information obtained from a population of hidden users is important and complementary to the results of the studies carried out in center for taking care of addiction problems (CSAPA) and support centres for the reduction of drug-related harms (CAARUD), by the ANRS (The French agency for AIDS and viral hepatitis research) 14059s Coquelicot study.

Furthermore, the investigators hypothesize that the multicentric implementation of this screening and treatment strategy will be facilitated by the use of a toolkit. This toolkit "ICONE" has been developed by the investigating team of the ANRS 95050 ICONE study.

Finally, the investigators hypothesize that the proposal to initiate psychiatric follow-up at the site of the RDS will have an effect on the insertion into city mental health care in the months following the RDS in PWUD with psychiatric comorbidities.

Principal objective:

The main objective 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 PWUD in Paris, Marseille, Lyon and Fort-de-France.

Secondary objectives:

• Estimate the size of the PWUD population in the 4 cities;
• Determine the prevalence of chronic HCV infection in the PWUD population in the 4 cities;
• Estimate the steps in the retrospective HCV care cascade (positive HCV Rapid Diagnostic Test (RDT), known HCV status, previously initiated antiviral therapy, undetectable viral load) ;
• Determine the factors associated with hepatitis C treatment failure: defined as a detectable viral load 12 weeks after the end of treatment;
• Estimate the cost of our intervention for one PWUD screened and one PWUD cured of hepatitis C;
• Estimate the prevalence of HIV infection among PWUDs in the 4 cities;
• Estimate the steps in the retrospective care cascade of HIV infection (known HIV status, previously initiated antiviral treatment, undetectable viral load);
• Estimate the prevalence of chronic hepatitis B among PWUD in the 4 cities;
• Estimate the prevalence of sexually transmitted infections (STIs) (Syphilis, Gonorrhoea, Chlamydia) among PWUD in Fort-de-France;
• Describe the most frequent psychological comorbidities in the PWUD population in the 4 cities;
• Evaluate the effectiveness of peer-supported referral to infectious (HIV, HCV, HBV at all sites and STIs only in Fort-de-France), psychiatric and addictive care;
• To 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).

All of these objectives will be analyzed specifically in the sub-population of crack cocaine users.

Qualitative study objectives Evaluate the acceptability of the RDS model and the relevance of an implementation strategy.

Methodology:

Hybrid effectiveness-implementation study type 2, allowing to evaluate simultaneously the effectiveness of the model on clinical criteria of access to psychiatric, addictological and infectious diseases care, and its feasibility by measuring the levers and potential obstacles to its implementation.

For the qualitative part, the investigators will conduct 15 interviews per site, i.e. 60 semi-structured interviews with the PWUDs who participated in the RDS. The researchers will organize 1 focus group with the stakeholders of each site before and after the implementation of the RDS.

Intervention:

Recruitment of PWUDs will be done through an RDS method. Ten to fifteen "seeds" will be selected per city for their diversity and social network. They will be invited to the research site (temporary community care facility), participate in all study procedures, and then receive 2-3 coupons to recruit eligible peers. Participants will receive HCV/HIV/HBV screening, on-site HCV RNA testing, liver fibrosis measurement, rapid antiviral (HCV) treatment initiation, treatment monitoring, and risk and harm reduction tools related to their risky practices. Participants with an HIV and/or HBV positive RDT will be referred to infectious disease services and the referral will be assessed. An assessment of psychological disorders will be carried out by i) Quick Screening Tool (QST) questionnaire asked to all participants; ii) MINI questionnaire for participants with positive QST. In case of a positive MINI, psychiatric consultations will be offered on site (Paris and Fort-de-France) or participants will be referred to structures offering psychiatric care (Lyon, Marseille). The effectiveness of referral to psychiatric care between the two interventions will be compared. All RDS participants will be referred to permanent addiction facilities and this referral will be evaluated. Peers will be present at this unique facility and will accompany participants throughout their HCV treatment. A capture/recapture study, nested within the RDS, will provide a reliable estimate of the PWUD population in the Paris arrondissements covered by the RDS and the cities of Marseille, Lyon and Fort-de-France. The qualitative study will take place at all sites. Individual interviews for a total of 60 participants will be conducted, as well as focus groups with stakeholders in each site.

Statistical methods:

Categorical variables will be described in terms of numbers and percentages with their associated 95% confidence intervals calculated using the exact method. Comparisons will be carried out by Chi² or Fisher's exact tests. Continuous variables will be described in terms of numbers, median, range and interquartile range or mean, standard deviation, standard deviation of the mean and confidence interval. Comparisons will be carried out using Mann-Whitney or Student's t tests depending on the distribution of the variable. The estimation of the size of the drug user populations will use the method recommended by the WHO (World Health Organization) with the Lincoln-Peterson estimator. Missing data will be taken into account by adopting the most penalizing approach. Logistic regression models will be used to search for factors associated with treatment failure. Multivariate logistic regression models will be employed to compare the success of psychiatric referral between the two groups.

Anticipated schedule:

Expected start date of the research (opening of RDS): September 2023 Duration of inclusions: 3 or 4 months per site (not necessarily over the same period) Duration of participation per participant: 1 day to 9 months Total expected duration of research: 24 months Anticipated end date of the trial/research: September 2025

Timeline for follow-up of participants in the research:

Participants with HCV RNA positive at RDS will be followed until SVR12 from treatment initiation. Visits at S4, end of treatment and SVR12.

• Study Type: Interventional
• Enrollment (Estimated): 3400
• Phase: Not Applicable

Contacts and Locations

Study Locations

• France
  • Auvergne-Rhône-Alpes
    • Lyon, Auvergne-Rhône-Alpes, France, 69000
      • Lyon
  • PACA
    • Marseille, PACA, France, 13000
      • Marseille
  • Île-de-France Region
    • Paris, Île-de-France Region, France, 75000
      • Paris
• Martinique
  • Martinique
    • Fort-de-France, Martinique, Martinique, 97200
      • Martinique

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes

Description

Inclusion criteria:

• Age > 18 years;
• Person who uses drugs, defined as:
• Reported psychoactive substance use and
• Positive urine test for at least one of the following: heroin, amphetamines, cocaine, MDMA (methylenedioxymethamphetamine), ecstasy, or misused opioid medications (methadone, buprenorphine or opiates used for a reason other than its original prescription (effects seeking) or used in a way that does not comply with its marketing authorisation (injected, snorted, taken multiple times beyond the prescribed dosage)) ;
• Informed and signed consent

Exclusion criteria:

• Inability to understand the study;
• Being under guardianship, curatorship or mandate of future protection;
• Person participating in another research study with an exclusion period still in progress at the time of pre-inclusion.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Intervention; Community-based intervention with screening and treatment initiation for HCV elimination among PWUD	Other: Hybrid effectiveness-implementation study type 2; Diagnosis of hepatitis C; Assessment of hepatic fibrosis; Treatment of hepatitis C; Assessment of psychological disorders and treatment or referral.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Percentage of HCV cured PWUD participants (SVR12) among those with a positive HCV viral load at baseline	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.	12 weeks after the end of the 2 to 3 months HCV treatment
Acceptability and relevance of the RDS and implementation strategy : a qualitative study	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).	From before the RDS implementation until the end of the study, up to 2 years

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of PWUD in the arrondissements of Paris (neighborhoods involved in seed distribution), and the cities of Lyon, Marseille and Fort-de-France	Estimated 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
Proportion of participants with positive HCV RNA among all participants	Number of participants with a positive HCV RNA divided by the number of participants	At baseline
Assessment of HCV cascade of care at inclusion : participants with a positive HCV RDT	Number of participants with a positive HCV RDT	At baseline
Assessment of HCV cascade of care at inclusion : participants with known HCV status	Number of participants with known HCV status (declarative) among participants with a positive HCV RDT	At baseline
Assessment of HCV cascade of care at inclusion : participants who were treated for HCV	Number of participants who were treated for HCV (self-reported) among participants with known HCV status	At baseline
Assessment of HCV cascade of care at inclusion : participants with known chronic hepatitis C status and undetectable HCV RNA	Number of participants with known chronic hepatitis C status and undetectable HCV RNA among participants who were treated for HCV	At baseline
HCV treatment failure defined as detectable viral load 12 weeks after HCV treatment completion	HCV treatment failure defined as detectable HCV RNA viral load measured in a veinous sample by quantitative PCR 12 weeks after the end of the antiviral treatment	12 weeks after the end of the 2 to 3 months HCV treatment
Cost of the intervention per screened participant	All costs of the intervention divided by the number of participants screened	Through study completion, an expected time frame of 2 years
Cost of the intervention per participant cured of hepatitis C	All costs of the intervention divided by the number of participants cured of hepatitis C	Through study completion, an expected time frame of 2 years
Proportion of participants with a positive HIV RDT among participants	Number of participants with a positive HIV RDT divided by the number of participants	At baseline
HIV care cascade assessment at inclusion : participants with known HIV status	Number of participants with known HIV status	At baseline
HIV care cascade assessment at inclusion : HIV-positive participants on antiretroviral therapy	Number of HIV-positive participants on antiretroviral therapy among participants with known HIV status	At baseline
HIV care cascade assessment at inclusion : participants on effective antiretroviral therapy	Number of participants on effective antiretroviral therapy (HIV RNA < 50 copies/ml) among HIV-positive participants on antiretroviral therapy	At baseline
Proportion of participants with detectable HBsAg	Number of participants with detectable HBsAg divided by the number of participants	At baseline
Proportion of participants in Fort-de-France with a positive PCR for gonorrhea	Number of participants in Fort-de-France with a positive PCR for gonorrhea divided by the number of participants in Fort-de-France	At baseline
Proportion of participants in Fort-de-France with a positive PCR for chlamydia	Number of participants in Fort-de-France with a positive PCR for chlamydia divided by the number of participants in Fort-de-France	At baseline
Proportion of participants in Fort-de-France with a positive test for syphilis	Number of participants in Fort-de-France with a positive test for syphilis divided by the number of participants in Fort-de-France	At baseline
Prevalence of psychological pathologies	Prevalence of psychological pathologies diagnosed by the MINI questionnaire (nurse trained beforehand notably on the psychosis module) with the use of 3 modules: Major depressive episode, psychotic disorders and suicidal risk following the positive QST questionnaire	At baseline
Success of infectious diseases referral	Proportion of participants referred to an infectious diseases structure who went to their consultation	At 6 months
Success of addictological referral	Proportion of participants referred to an addictological structure who went to their consultation	At 6 months
Success of psychiatric referral at 3 months	Proportion of participants referred to a psychiatric structure in the city who went to their consultation	At 3 months
Success of psychiatric referral at 6 months	Proportion of participants referred to a psychiatric structure in the city who went to their consultation	At 6 months

Collaborators and Investigators

• Sponsor: ANRS, Emerging Infectious Diseases
• Investigators: Principal Investigator: Hélène Donnadieu, PhD, PCCEI

Study record dates

Study Major Dates

• Study Start (Actual): October 2, 2023
• Primary Completion (Actual): May 16, 2025
• Study Completion (Estimated): September 30, 2025

Study Registration Dates

• First Submitted: March 6, 2023
• First Submitted That Met QC Criteria: March 20, 2023
• First Posted (Actual): April 3, 2023

Study Record Updates

• Last Update Posted (Estimated): September 8, 2025
• Last Update Submitted That Met QC Criteria: September 2, 2025
• Last Verified: September 1, 2025

More Information

Terms related to this study

• Keywords: mental health; Hepatitis C Virus; RDS; peers; Test and Treat; People who use drugs
• Additional Relevant MeSH Terms: Blood-Borne Infections; Mental Disorders; Infections; RNA Virus Infections; Virus Diseases; Digestive System Diseases; Liver Diseases; Hepatitis, Viral, Human; Communicable Diseases; Chemically-Induced Disorders; Flaviviridae Infections; Hepatitis; Behavior; Personal Satisfaction; Substance-Related Disorders; Hepatitis C; Psychological Well-Being
• Other Study ID Numbers: ANRS 0336s ICONE 2

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Plan Description: All collected individual participant data
• IPD Sharing Time Frame: After publication and for 15 years.
• IPD Sharing Access Criteria: Open to anyone at https://recherche.data.gouv.fr/

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No