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Clinical Trials/NCT04156945
NCT04156945Active, not recruitingNot Applicable

Interventions to Curb Hepatitis C Reinfections Among Men Who Have Sex With Men

Public Health Service of Amsterdam25 sites in 2 countries258 target enrollmentStarted: September 14, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Enrollment
258
Locations
25
Primary Endpoint
Change in the proportion at risk for HCV infection (as determined by a HCV-MOSAIC risk ≥ 2.0).

Study Overview

Brief Summary

Men who have sex with men (MSM) who cured from hepatitis C virus (HCV) infection are at substantial risk of HCV reinfection. In this study, the investigators aim to evaluate the effectiveness of an online behavioural intervention, a home-based testing intervention and a combination of both on risk behaviour, and ultimately preventing HCV reinfection and onward spread of HCV.

Detailed Description

Rationale: As highly effective therapy against hepatitis C virus (HCV) infection is available with rapid uptake, there is newfound optimism for HCV elimination. Nevertheless, HCV reinfections cause great concern in at risk populations, including men who have sex with men (MSM). In the Netherlands, MSM account for the majority of new HCV (re)infections. Although HCV treatment uptake is high in this group, modelling data indicate HCV elimination would not be feasible without a reduction in risk behaviour. This finding highlights the urgent need for effective interventions aimed at reducing risk behaviour and preventing reinfections in MSM.

Objective: To evaluate interventions aimed at reducing risk behaviour, and ultimately preventing HCV reinfections and onward spread of HCV.

Study design: Using a 3-arm randomised trial comparing run-in and intervention periods, we will evaluate the effect of two interventions and its combination on risk behaviour in MSM previously infected with HCV.

Study population: MSM aged 18 years or older with a history of a successfully treated or spontaneously cleared HCV infection.

Interventions: Intervention I is a targeted, online behavioural intervention developed as part of the project. Intervention II aims to increase the frequency of testing by offering an additional patient-initiated, home-based HCV RNA testing service with the use of self-sampled dried blot spots. Intervention III is a combination of intervention I and II.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Male
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Informed consent documented by signature.
  • Male individual aged 18 years or older.
  • History of a cured or spontaneously cleared HCV infection (positive HCV RNA test in the past and/or positive anti-HCV IgG).
  • Self-reported MSM who are either (i) HIV-positive seeking care at an HIV treatment center or (ii) HIV-negative and seeking care at an STI/PrEP/sexual health center.
  • Sufficient understanding of Dutch or English.
  • Have internet access and an e-mail address.

Exclusion Criteria

  • Acute or chronic HCV infection at time of enrolment.
  • Under HCV treatment at time of enrolment.
  • Unlikely, in the opinion of the clinician, to comply with the study procedures.
  • Currently participating in an intervention study that offers extra HCV testing and/or a behavioural intervention targeting risk behaviour.
  • Investigators or otherwise dependent persons.

Outcomes

Primary Outcomes

Change in the proportion at risk for HCV infection (as determined by a HCV-MOSAIC risk ≥ 2.0).

Time Frame: Run-in period (0-6 months) versus intervention period (6-24 months)

From run-in and post-randomization questionnaires, we will evaluate the proportion at risk of HCV infection (as determined by a HCV-MOSAIC score ≥ 2.0) during the run-in versus intervention periods. The HCV-MOSAIC risk score has been previously validated for acute HCV-infection and is calculated by summing up the beta-coefficients specific to six self-reported risk factors when present in the past 6 months: (i) receptive condomless anal sex (beta 1.1), (ii) sharing sex toys (beta 1.2), (iii) unprotected fisting (beta 0.9), (iv) injecting drug use (beta 1.4), (v) sharing snoring equipment during nasally-administered drug use (beta 1.0), and (vi) ulcerative sexually transmitted infection (beta 1.4).

Secondary Outcomes

  • Change in the proportion of individuals reporting receptive condomless anal sex.(Month 0, month 6, month 12, month 18, month 24)
  • Incidence rate of HCV reinfection.(Self-reported: month 0, month 6, month 12, month 18, month 24. Laboratory data: during total follow-up period of 2 years.)
  • Change in the proportion of individuals sharing sex toys.(Month 0, month 6, month 12, month 18, month 24)
  • Change in the proportion of individuals reporting unprotected fisting.(Month 0, month 6, month 12, month 18, month 24)
  • Incidence rate of any STI.(Month 0, month 6, month 12, month 18, month 24)
  • Change in the number of sex partners.(Month 0, month 6, month 12, month 18, month 24)
  • Change in the number of condomless anal sex acts with casual partners.(Month 0, month 6, month 12, month 18, month 24)
  • Change in the proportion of individuals reporting injection drug use.(Month 0, month 6, month 12, month 18, month 24)
  • Change in the proportion of individuals sharing snoring equipment during nasally-administered drug use.(Month 0, month 6, month 12, month 18, month 24)
  • Change in the proportion of individuals reporting ulcerative sexually transmitted infection*.(Month 0, month 6, month 12, month 18, month 24)
  • Change in the frequency of individuals engaging in group sex activities, including changes in number of events and maximum number of sex partners during an event.(Month 0, month 6, month 12, month 18, month 24)
  • Change in the proportion of individuals sharing lubricants.(Month 0, month 6, month 12, month 18, month 24)
  • Change in the proportion of individuals disinfecting sex toys, skin and/or sex location.(Month 0, month 6, month 12, month 18, month 24)
  • Change in sexual wellbeing score.(Month 0, month 6, month 12, month 18, month 24)
  • Proportion of individuals with change in any of the items of the HCV-MOSAIC risk score.(Month 0, month 6, month 12, month 18, month 24)
  • Change in the frequency of recreational drug use before and during sex.(Month 0, month 6, month 12, month 18, month 24)
  • Change in the proportion of individuals sharing anal douches.(Month 0, month 6, month 12, month 18, month 24)

Investigators

Sponsor
Public Health Service of Amsterdam
Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Prof. dr. Maria Prins

Prof. dr.

Public Health Service of Amsterdam

Study Sites (25)

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