Hepatitis CNCT06203925
Hepatitis C Virus Self-testing (HCVST) in Sexual and Gender Minorities in Rio de Janeiro
An observational study of Hepatitis C, run by Oswaldo Cruz Foundation at 1 site in Brazil.
Trial summary
Sexual and gender minorities (SGM), such as gay, bisexual and other men who have sex with men (MSM) and transgender women (TGW), are at high risk of HCV infection. A recently released guideline by the WHO recommended HCVST to scale-up HCV screening. Read more about this study
- Who is it for?
- Ages 18 to 99 yearsHealthy volunteers can take part
- Conditions the study is for
- Hepatitis C
- What is being tested?
- Hepatitis C virus self-test (oral fluid HCVST) and Hepatitis C virus self-test (blood-based HCVST)
- Type of treatment
- Pill or oral medicine
- How many people
- 3,000 participants
- Where
- 1 siteBrazil
- Study dates
- 8 Jan 2024to 31 Dec 2025
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 99 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Primary Study: Participants reported residence in the metropolitan area of Rio de Janeiro (municipalities of Rio de Janeiro, Duque de Caxias, São João de Meriti, Belford Roxo, Nilópolis, Mesquita, Nova Iguaçu, Queimados, Japeri, Paracambi, Seropédica, Itaguaí, Magé, Guapimirim, Niterói, São Gonçalo, Itaboraí, Seropédica, Rio Bonito, Tanguá and Maricá) Ancillary Study: 2. Self-identification as MSM or TGW 3. Presential visit for PrEP (initiation or follow-up) at INI/FIOCRUZ
Who may be able to join
- Age ≥ 18 years old with knowledge of the Portuguese language
- Self-identification as gay, bisexual and other cisgender MSM, TGW, transgender men, and gender nonbinary/diverse individuals
- Reported residence in the metropolitan area of Rio de Janeiro (municipalities of Rio de Janeiro, Duque de Caxias, São João de Meriti, Belford Roxo, Nilópolis, Mesquita, Nova Iguaçu, Queimados, Japeri, Paracambi, Seropédica, Itaguaí, Magé, Guapimirim, Niterói, São Gonçalo, Itaboraí, Seropédica, Rio Bonito, Tanguá and Maricá)
Who cannot join
- 1. Unable or not willing to provide informed consent
Trial locations and contacts
1 site in 1 country.
Brazil1 site
Evandro Chagas National Institute of Infectious Diseases
Rio de Janeiro, Rio de Janeiro/RJ, 21040-360
About this study
Official title: Hepatitis C Virus Self-testing (HCVST) in Sexual and Gender Minorities in Rio de Janeiro (Brazil): Distribution and Uptake of HCV Testing Using Internet Technology and Evaluation of Usability of HCVST
Sexual and gender minorities (SGM), such as gay, bisexual and other men who have sex with men (MSM) and transgender women (TGW), are at high risk of HCV infection. A recently released guideline by the WHO recommended HCVST to scale-up HCV screening. However, data on delivery-services of HCVST kits and uptake of HCV testing using HCVST remain scarce in Latin American countries. Additionally, data on the usability of HCVST in MSM/TGW, especially blood-based tests, still lacking in Brazil. To evaluate the uptake of HCV testing by the strategy of using HCVST ordered by the internet and delivery by the post in key populations (SGM) living in the metropolitan region of Rio de Janeiro (Brazil). Additionally, an Ancillary study will assess the usability of different kits of HCVST in MSM/TGW using PrEP.
Study Design and Population: This protocol will be composed of two studies that will be conducted in parallel. The primary study will be a cohort study in which SGM ≥ 18 years old living in the metropolitan area of Rio de Janeiro who request HCVST will be included. The Ancillary study will be a cross-sectional study where adult MSM or TGW attending a presential visit for PrEP (initiation or follow-up) at INI/FIOCRUZ will be eligible for this study. The investigators estimate that 3,000 persons will request home-delivery of HCVST (Primary study) and 250 participants will be included in the Ancillary study.Study Design and Population: This protocol will be composed of two studies that will be conducted in parallel. The primary study will be a cohort study in which SGM ≥ 18 years old living in the metropolitan area of Rio de Janeiro who request HCVST will be included. The Ancillary study will be a cross-sectional study where adult MSM or TGW attending a presential visit for PrEP (initiation or follow-up) at INI/FIOCRUZ will be eligible for this study. The investigators estimate that 3,000 persons will request home-delivery of HCVST (Primary study) and 250 participants will be included in the Ancillary study.
Read more
Methods: For the Primary Study, a web-based platform will be built for this project and an educational campaign will be developed in dating apps to encourage HCV testing. The web platform will contain modules with information on HCV infection and a log-in to request HCV self-tests that can be delivered by the post or collected in the centralized pharmacy for HCV testing. People will be encouraged to report their HCVST results in the online platform. People with positive HCV antibody will be linked-to-care for HCV infection confirmation and treatment initiation. For the Ancillary Study, MSM/TGW attending presential visits for PrEP at INI/FIOCRUZ will be invited to perform HCVST (blood-based and oral fluid tests) under supervision of a trained healthcare worker. Participants will read written instructions and watch a video explaining the procedures step-by-step for HCVST. A second HCV test using the same kit will be performed by the healthcare worker for concordance analysis. People with positive HCV antibodies will be linked to HCV infection confirmation and treatment initiation.
Data analysis: Descriptive statistical analysis will be used to evaluate the characteristics of people seeking HCVST, participant's preferences, uptake of HCV testing using self-test kits and internet technologies, as well as acceptability, usability and result interpretation of HCVST in a sub-sample of participants. Ethical considerations: Locally, ethics approval will be obtained from the INI/FIOCRUZ. International ethics clearance will be obtained from the World Health Organization Ethics Review Committee (WHO ERC). All participants will be informed of risks and benefits of the procedures and that their participation is voluntary. All participants will be required to sign the informed consent (an online agreement for Primary Study) as required by Brazilian regulations to participate in research studies. All data collected will respect The Brazilian General Data Protection Law (Law nº 13.709/2018).
Read the detailed description
Chronic hepatitis C is a major health issue in Brazil where it is estimated that up to 650,000 people are living with HCV infection. Despite the availability of rapid tests as well as universal access to safe and highly effective drugs for HCV treatment for free of charge, the HCV HCV continuum of care remains unsatisfactory. HCV transmission due to sexual activities are increasing in Brazil, especially among young men. It is well known that MSM and/or TGW are at high risk for HCV infection. HCV infection in these key populations might occur mainly in the context of traumatic sex practices that increase the risk of blood-blood contact. The use of drug prior to or during sex (chem-sex) might be associated with HCV infection. Few studies have reported the prevalence of HCV infection among SGM in Brazil. Firstly, a single center study that included a limited sample (n=522) using Respondent-Driven Sampling reported a prevalence of anti-HCV positive of 1.3% (95%CI: 0.3-5.5) in MSM in Central region. All people with anti-HCV positive reported high-risk sexual behaviors, condomless use at anal intercourse and frequent chem-sex [39]. More recently, the prospective, single-arm, open-label, multicentre PrEP implementation study conducted in Brazil (14 sites), Mexico (4 sites), and Peru (10 sites) included 9,509 HIV-negative MSM and TGW for daily oral initiation of PrEP. Prevalence of hepatitis C increased from the enrolment to week-52 among participants from Mexico and Peru, cisgender men, and those aged 25-30 years. In Brazil (n=3,928), the prevalence of HCV infection was 0.34% (95%CI 0.16-0.52) and 0.58% (95%CI 0.24-0.91) at enrolment and week-52, respectively [40]. Similarly, a Brazilian study reported an HCV prevalence of 0.66% (anti-HCV positive in 340 from 51,486 tests) in key populations (MSM, transgender people, people who inject drugs, and sex workers) in Curitiba (Southern region) [24] Similar to other countries, HIV coinfection and injection drug use have been associated with increased risk of HCV infection/reinfection in Brazil. Prevalence of HCV infection (2.7%) was mostly associated with injection drug use in the last year [OR=10.33 (95%CI 4.74-22.52)] and HIV infection [OR=4.74 (95%CI 1.82-12.36)] in Brazilian men prisoners (n=2,848)[41].
Large scale screening for hepatitis C in high-risk people and linkage-to-care are cornerstones towards to HCV elimination. HCVST can decrease the barriers to traditional testing by increasing convenience and privacy. Lesson learned with HIVST can be informative and suggest that this new/additional testing approach may help to increase HCV testing and linkage to care and treatment. A recently released guideline by the WHO recommended HCVST to scale-up HCV screening [6]. In brief, this guideline recommends that HCVST should be offered as an additional approach to facility-based HCV testing. Additionally, HCVST needs to be followed by confirmation of viremic infection (HCV-RNA), and linkage-to-treatment, and HCVST service delivery should be adapted to local context, which includes community preferences. However, the usability of HCVST kits, cost-effective, non-discriminatory and inclusive service delivery and optimal position of HCVST in national HCV programs must be addressed. Stigma is an important element in the experience of living with chronic HCV infection, especially in SGM persons. This stigma impacts in healthcare access and uptake as well as health outcomes. The use of HCVST can help to mitigate the stigma along the HCV continuum of care. Additionally, the immediate linkage to care after a positive HCVST using telehealth might reduce mental distress from positive results.
Recent studies have evaluated the usability, acceptability, and rates of interpretation of results from different kits (blood-based and oral fluid) of HCVST worldwide. Few studies reported high acceptability and usability of oral-fluid HCVST in key populations (mostly MSM), especially in the USA, European countries and Asia. However, data on delivery-services of HCVST kits and uptake of HCV testing using HCVST remain scarce in Latin American countries. Additionally, data on the usability of HCVST in MSM/TGW, especially blood-based tests, still lacking in Brazil. This study will evaluate the uptake of HCV testing by the strategy of using HCVST that would be able to be ordered by the internet and delivery by the post in key populations (SGM) living in the metropolitan region of Rio de Janeiro (Brazil). Additionally, a sub-study will assess the acceptability, usability and result interpretation of different kits of HCVST in MSM/TGW using PrEP in a reference center in Rio de Janeiro (Brazil).
This project will assess operational research priorities about HCVST in Brazil. The investigators expect to fulfill gaps of knowledge on product optimization (acceptability and usability of blood-based and oral fluid HCVST kits), service delivery and linkage pathways to confirmatory testing and treatment after reactive HCVST results in one of the largest agglomerations worldwide, such as the metropolitan area of Rio de Janeiro (Brazil). The investigators expect to increase HCV testing by using an online platform to inform about HCV infection where people will be able to order HCVST that can be delivered by the post. Additionally, our strategy will include an offer of HIVST with HCVST (combo HIV/HCVST) to increase interest for HCV testing and a massive advertising campaign in dating-apps used by SGM (e.g. Grindr, Scruff and Hornet). In addition, the investigators expect that HCVST will be highly accepted and easy to be performed among PrEP users in Rio de Janeiro (Brazil).
This protocol will be composed by a Primary Study and an Ancillary Study that will be conducted in parallel.
OBJECTIVES:
The Primary Study will assess HCVST using internet-technologies among SGM. The main hypothesis of the Primary Study is that HCVST ordered in an online platform and delivered by the post will increase HCV testing uptake among SGM.
The Ancillary Study will assess the acceptability and usability of different kits of HCVST in MSM/TGW under PrEP. The main hypothesis of the Ancillary Study is that blood-based and oral fluid HCVST will be well accepted and easily to be performed among MSM/TGW under PrEP in a referral center in Rio de Janeiro (Brazil)
2.1. Overall objectives Overall objective of the Primary Study: To evaluate the uptake of HCV testing using HCVST ordered through a web-based platform among SGM living in Rio de Janeiro (Brazil) Overall objective of the Ancillary Study: To evaluate the acceptability, usability, results interpretation and participant's perspectives of HCVST with blood-based and oral-fluid kits among MSM and TGW who are attending a PrEP visit in a reference center in Rio de Janeiro (Brazil).
2.2 Specific objectives
Specific objectives of the Primary Study:
- To describe socio-demographic characteristics of people seeking HCV self-testing
- To evaluate preference for oral fluid or blood-based HCV self-tests
- To evaluate the proportion of people using home-based delivery vs pick up of HCV self-tests
- To evaluate the proportion of people reporting HCV self-test results
- To evaluate the proportion of people attending a consultation when HCV self-test is reactive or invalid
- To evaluate the knowledge of SGM about HCV infection and/or treatment
- To evaluate cost per case of HCV infection detected using HCV self-testing and internet technologies
- To evaluate the proportion of people with reactive HCVST who had HCV-RNA test for confirmation and who started HCV treatment (linkage to HCV continuum of care)
- To evaluate the proportion of people who ordered HCVST to receive an HIVST kit
Specific objectives of the Ancillary Study:
- To describe socio-demographic characteristics of people under PrEP performing HCVST
- To evaluate the proportion of people who correctly perform HCVST
- To evaluate the proportion of people who do not need assistance to correctly perform HCVST
- To evaluate the proportion of people who correctly report HCVST results (re-read by a trained healthcare worker)
- To evaluate the concordance of HCVST with re-testing by a trained healthcare worker
- To evaluate the preference for oral-fluid or blood-based HCVST kits
- To evaluate the proportion of people attending a consultation when HCV self-test is reactive or invalid
- To evaluate the knowledge of people under PrEP about HCV infection and/or treatment
- To evaluate cost per case of HCV infection detected using HCVST in PrEP users
- To evaluate the proportion of people with reactive HCVST who had HCV-RNA test for confirmation and who started HCV treatment (linkage to HCV continuum of care)
- Conditions
- Hepatitis C
- Being tested
- Hepatitis C virus self-test (oral fluid HCVST), Hepatitis C virus self-test (blood-based HCVST)
- Keywords
- Hepatitis C virus self-test, Sexual and Gender Minorities
- Medical subject headings
- Hepatitis C, Coitus
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Hepatitis C virus self-test (oral fluid HCVST)Diagnostic test
Also called OraSure Technologies, Inc, Bethlehem, PA
The participant will be able to choose between oral-fluid or blood-based HCVST. The package will include an HCV OraQuick ® HCV Self-Test kit, (OraSure Technologies, Inc, Bethlehem, PA) or a Wondfo® HCV Self-Test (Guangzhou, P.R. China) at Primary Study.
At Ancyllary study, the individuals attending PrEP consultations at INI/FIOCRUZ will be invited to perform HCVST using blood-based and oral-fluid kits.
Hepatitis C virus self-test (blood-based HCVST)Diagnostic test
Also called Wondfo® HCV Self-Test (Guangzhou, P.R. China)
The participant will be able to choose between oral-fluid or blood-based HCVST. The package will include an HCV OraQuick ® HCV Self-Test kit, (OraSure Technologies, Inc, Bethlehem, PA) or a Wondfo® HCV Self-Test (Guangzhou, P.R. China) at Primary Study. At Ancylary Study, the individuals attending PrEP consultations at INI/FIOCRUZ will be invited to perform HCVST using blood-based and oral-fluid kits.
| Study group | Role | What they receive |
|---|---|---|
| Primary Study | The study will be a cohort study. Adult SGM living in the metropolitan area of Rio de Janeiro who voluntary want to perform HCV testing ordered through a web-based platform will be eligible for this study. SGM will be defined by gay, bisexual and other cisgender MSM, TGW, transgender men, and gender nonbinary/diverse individuals. Receives: Diagnostic Test: Hepatitis C virus self-test (oral fluid HCVST); Diagnostic Test: Hepatitis C virus self-test (blood-based HCVST) | |
| Ancillary Study | The study will be a cross-sectional study. Adult MSM or TGW attending a presential visit for PrEP (initiation or follow-up) at INI/FIOCRUZ will be eligible for this study. Receives: Diagnostic Test: Hepatitis C virus self-test (oral fluid HCVST); Diagnostic Test: Hepatitis C virus self-test (blood-based HCVST) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of SGM living in Rio de Janeiro (Brazil) who requested an HCVST kit through a web-based platform
Captured datas obtained from a web-based plataform
Measured: 1 month
Number of SGM living in Rio de Janeiro (Brazil) who received and performed the test.
Captured datas obtained from a web-based plataform
Measured: 1 month
Proportion of MSM/TGW who correctly performed HCVST with oral-fluid and blood-based kits without assistance of a healthcare worker
Captured datas obtained from a web-based plataform
Measured: 1 day
Secondary outcomes (18)
Socio-demographic characteristics through the data obtained from the study.
- Socio-demographic characteristics of SGM seeking HCVST in Rio de Janeiro
Measured: 2 months
Type-preference test through the data obtained from the study.
- Proportion of type-preference [oral fluid vs blood-based; home-based delivery vs pick-up] for HCVST
Measured: 2 months
Participants who reported Easy test.
- Proportion of people who reported HCVST as "Easy/Very Easy" to be performed
Measured: 2 months
Possible outcomes through the data obtained from the study.
- Proportion of people reporting HCVST results at the web-based platform
Measured: 2 months
Participants through the data obtained from the study.
- Proportion of people correctly interpreting HCVST results
Measured: 2 months
Participants who attending a consultation through the data obtained from the study.
- Proportion of people attending a consultation after an HCVST result as reactive or invalid
Measured: 2 months
Prevalence of reactive HCV through the data obtained from the study.
- Prevalence of reactive HCV antibody by HCVST in SGM in Rio de Janeiro
Measured: 2 months
Cost per identification through the data obtained from the study.
- Cost per identification of chronic hepatitis C individual using HCVST
Measured: 2 months
Particiopants who used telehealth through the data obtained from the study.
- Proportion of people who accepted and used telehealth for linkage-to-care for HCV infection
Measured: 2 months
Socio-demographic characteristics of MSM/TGW through the data obtained from the study.
- Socio-demographic characteristics of MSM/TGW who agreed to perform HCVST
Measured: 1 month
Participants who report the test through the data obtained from the study.
- Proportion of people who correctly report HCVST results (using re-reading by a trained healthcare worker as the reference)
Measured: 1 month
Participants who needed help from a healthcare.
- Proportion of case where results of HCV re-testing by a trained healthcare worker was concordance with HCVST using the same kit
Measured: 1 month
Preference for tests
- Proportion of type-preference [oral fluid vs blood-based] for HCVST
Measured: 1 month
Easy test
- Proportion of people who reported HCVST as "Easy/Very Easy" to be performed
Measured: 1 month
Participants who needed a consultation.
- Proportion of people attending a consultation after an HCVST result as reactive or invalid
Measured: 1 month
Positive participants
- Prevalence of reactive HCV antibody by HCVST in MSM/TGW attending a PrEP visit
Measured: 1 month
Cost for using the test
- Cost per identification of chronic hepatitis C individual using HCVST in a PrEP scenario
Measured: 1 month
Positive participants with HCV-RNA
- Proportion of people with reactive HCVST who had HCV-RNA test for confirmation and who started HCV treatment (linkage to HCV continuum of care)
Measured: 1 month
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Jan 2024
- Study start8 Jan 2024 (estimated)
- Primary completion31 Dec 2025 (estimated)
- Study completion31 Dec 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Hepatitis CStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 3,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Oswaldo Cruz Foundation
- Sponsor type
- University, hospital or other
- Collaborators
- World Health Organization, UNITAID
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06203925
- Sponsor's protocol ID
- 69747223.4.0000.5262
- Status last verified
- Dec 2023
- First submitted
- 12 Dec 2023
- Last updated
- 12 Jan 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
- Individual data sharing
- No: There is a risk of loss of participant confidentiality and there is no authorization from the ethics committee to make individual data available. All data will be made available through scientific publications.
Study at a glance
From the registry record, last updated by the sponsor on 12 Jan 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Hepatitis C Virus Self-testing (HCVST) in Sexual and Gender Minorities in Rio de Janeiro (Brazil): Distribution and Uptake of HCV Testing Using Internet Technology and Evaluation of Usability of HCVST
- ClinicalTrials.gov ID
- NCT06203925
- Acronym / sponsor ID
- 69747223.4.0000.5262
- Conditions
- Hepatitis C
- Keywords
- Hepatitis C virus self-test, Sexual and Gender Minorities
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 3,000 participants (estimated)
- Lead sponsor
- Oswaldo Cruz FoundationUniversity, hospital or other
- Collaborators
- World Health Organization, UNITAID
- Study start
- 8 Jan 2024 (estimated)
- Primary completion
- 31 Dec 2025 (estimated)
- Study completion
- 31 Dec 2025 (estimated)
- First posted
- 12 Jan 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Sexual and gender minorities (SGM), such as gay, bisexual and other men who have sex with men (MSM) and transgender women (TGW), are at high risk of HCV infection. A recently released guideline by the WHO recommended HCVST to scale-up HCV screening. However, data on delivery-services of HCVST kits and uptake of HCV testing using HCVST remain scarce in Latin American countries. Additionally, data on the usability of HCVST in MSM/TGW, especially blood-based tests, still lacking in Brazil. To evaluate the uptake of HCV testing by the strategy of using HCVST ordered by the internet and delivery by the post in key populations (SGM) living in the metropolitan region of Rio de Janeiro (Brazil). Additionally, an Ancillary study will assess the usability of different kits of HCVST in MSM/TGW using PrEP.
Study Design and Population: This protocol will be composed of two studies that will be conducted in parallel. The primary study will be a cohort study in which SGM ≥ 18 years old living in the metropolitan area of Rio de Janeiro who request HCVST will be included. The Ancillary study will be a cross-sectional study where adult MSM or TGW attending a presential visit for PrEP (initiation or follow-up) at INI/FIOCRUZ will be eligible for this study. The investigators estimate that 3,000 persons will request home-delivery of HCVST (Primary study) and 250 participants will be included in the Ancillary study.Study Design and Population: This protocol will be composed of two studies that will be conducted in parallel. The primary study will be a cohort study in which SGM ≥ 18 years old living in the metropolitan area of Rio de Janeiro who request HCVST will be included. The Ancillary study will be a cross-sectional study where adult MSM or TGW attending a presential visit for PrEP (initiation or follow-up) at INI/FIOCRUZ will be eligible for this study. The investigators estimate that 3,000 persons will request home-delivery of HCVST (Primary study) and 250 participants will be included in the Ancillary study.
Methods: For the Primary Study, a web-based platform will be built for this project and an educational campaign will be developed in dating apps to encourage HCV testing. The web platform will contain modules with information on HCV infection and a log-in to request HCV self-tests that can be delivered by the post or collected in the centralized pharmacy for HCV testing. People will be encouraged to report their HCVST results in the online platform. People with positive HCV antibody will be linked-to-care for HCV infection confirmation and treatment initiation. For the Ancillary Study, MSM/TGW attending presential visits for PrEP at INI/FIOCRUZ will be invited to perform HCVST (blood-based and oral fluid tests) under supervision of a trained healthcare worker. Participants will read written instructions and watch a video explaining the procedures step-by-step for HCVST. A second HCV test using the same kit will be performed by the healthcare worker for concordance analysis. People with positive HCV antibodies will be linked to HCV infection confirmation and treatment initiation.
Data analysis: Descriptive statistical analysis will be used to evaluate the characteristics of people seeking HCVST, participant's preferences, uptake of HCV testing using self-test kits and internet technologies, as well as acceptability, usability and result interpretation of HCVST in a sub-sample of participants. Ethical considerations: Locally, ethics approval will be obtained from the INI/FIOCRUZ. International ethics clearance will be obtained from the World Health Organization Ethics Review Committee (WHO ERC). All participants will be informed of risks and benefits of the procedures and that their participation is voluntary. All participants will be required to sign the informed consent (an online agreement for Primary Study) as required by Brazilian regulations to participate in research studies. All data collected will respect The Brazilian General Data Protection Law (Law nº 13.709/2018).
Detailed description
Chronic hepatitis C is a major health issue in Brazil where it is estimated that up to 650,000 people are living with HCV infection. Despite the availability of rapid tests as well as universal access to safe and highly effective drugs for HCV treatment for free of charge, the HCV HCV continuum of care remains unsatisfactory. HCV transmission due to sexual activities are increasing in Brazil, especially among young men. It is well known that MSM and/or TGW are at high risk for HCV infection. HCV infection in these key populations might occur mainly in the context of traumatic sex practices that increase the risk of blood-blood contact. The use of drug prior to or during sex (chem-sex) might be associated with HCV infection. Few studies have reported the prevalence of HCV infection among SGM in Brazil. Firstly, a single center study that included a limited sample (n=522) using Respondent-Driven Sampling reported a prevalence of anti-HCV positive of 1.3% (95%CI: 0.3-5.5) in MSM in Central region. All people with anti-HCV positive reported high-risk sexual behaviors, condomless use at anal intercourse and frequent chem-sex [39]. More recently, the prospective, single-arm, open-label, multicentre PrEP implementation study conducted in Brazil (14 sites), Mexico (4 sites), and Peru (10 sites) included 9,509 HIV-negative MSM and TGW for daily oral initiation of PrEP. Prevalence of hepatitis C increased from the enrolment to week-52 among participants from Mexico and Peru, cisgender men, and those aged 25-30 years. In Brazil (n=3,928), the prevalence of HCV infection was 0.34% (95%CI 0.16-0.52) and 0.58% (95%CI 0.24-0.91) at enrolment and week-52, respectively [40]. Similarly, a Brazilian study reported an HCV prevalence of 0.66% (anti-HCV positive in 340 from 51,486 tests) in key populations (MSM, transgender people, people who inject drugs, and sex workers) in Curitiba (Southern region) [24] Similar to other countries, HIV coinfection and injection drug use have been associated with increased risk of HCV infection/reinfection in Brazil. Prevalence of HCV infection (2.7%) was mostly associated with injection drug use in the last year [OR=10.33 (95%CI 4.74-22.52)] and HIV infection [OR=4.74 (95%CI 1.82-12.36)] in Brazilian men prisoners (n=2,848)[41].
Large scale screening for hepatitis C in high-risk people and linkage-to-care are cornerstones towards to HCV elimination. HCVST can decrease the barriers to traditional testing by increasing convenience and privacy. Lesson learned with HIVST can be informative and suggest that this new/additional testing approach may help to increase HCV testing and linkage to care and treatment. A recently released guideline by the WHO recommended HCVST to scale-up HCV screening [6]. In brief, this guideline recommends that HCVST should be offered as an additional approach to facility-based HCV testing. Additionally, HCVST needs to be followed by confirmation of viremic infection (HCV-RNA), and linkage-to-treatment, and HCVST service delivery should be adapted to local context, which includes community preferences. However, the usability of HCVST kits, cost-effective, non-discriminatory and inclusive service delivery and optimal position of HCVST in national HCV programs must be addressed. Stigma is an important element in the experience of living with chronic HCV infection, especially in SGM persons. This stigma impacts in healthcare access and uptake as well as health outcomes. The use of HCVST can help to mitigate the stigma along the HCV continuum of care. Additionally, the immediate linkage to care after a positive HCVST using telehealth might reduce mental distress from positive results.
Recent studies have evaluated the usability, acceptability, and rates of interpretation of results from different kits (blood-based and oral fluid) of HCVST worldwide. Few studies reported high acceptability and usability of oral-fluid HCVST in key populations (mostly MSM), especially in the USA, European countries and Asia. However, data on delivery-services of HCVST kits and uptake of HCV testing using HCVST remain scarce in Latin American countries. Additionally, data on the usability of HCVST in MSM/TGW, especially blood-based tests, still lacking in Brazil. This study will evaluate the uptake of HCV testing by the strategy of using HCVST that would be able to be ordered by the internet and delivery by the post in key populations (SGM) living in the metropolitan region of Rio de Janeiro (Brazil). Additionally, a sub-study will assess the acceptability, usability and result interpretation of different kits of HCVST in MSM/TGW using PrEP in a reference center in Rio de Janeiro (Brazil).
This project will assess operational research priorities about HCVST in Brazil. The investigators expect to fulfill gaps of knowledge on product optimization (acceptability and usability of blood-based and oral fluid HCVST kits), service delivery and linkage pathways to confirmatory testing and treatment after reactive HCVST results in one of the largest agglomerations worldwide, such as the metropolitan area of Rio de Janeiro (Brazil). The investigators expect to increase HCV testing by using an online platform to inform about HCV infection where people will be able to order HCVST that can be delivered by the post. Additionally, our strategy will include an offer of HIVST with HCVST (combo HIV/HCVST) to increase interest for HCV testing and a massive advertising campaign in dating-apps used by SGM (e.g. Grindr, Scruff and Hornet). In addition, the investigators expect that HCVST will be highly accepted and easy to be performed among PrEP users in Rio de Janeiro (Brazil).
This protocol will be composed by a Primary Study and an Ancillary Study that will be conducted in parallel.
OBJECTIVES:
The Primary Study will assess HCVST using internet-technologies among SGM. The main hypothesis of the Primary Study is that HCVST ordered in an online platform and delivered by the post will increase HCV testing uptake among SGM.
The Ancillary Study will assess the acceptability and usability of different kits of HCVST in MSM/TGW under PrEP. The main hypothesis of the Ancillary Study is that blood-based and oral fluid HCVST will be well accepted and easily to be performed among MSM/TGW under PrEP in a referral center in Rio de Janeiro (Brazil)
2.1. Overall objectives Overall objective of the Primary Study: To evaluate the uptake of HCV testing using HCVST ordered through a web-based platform among SGM living in Rio de Janeiro (Brazil) Overall objective of the Ancillary Study: To evaluate the acceptability, usability, results interpretation and participant's perspectives of HCVST with blood-based and oral-fluid kits among MSM and TGW who are attending a PrEP visit in a reference center in Rio de Janeiro (Brazil).
2.2 Specific objectives
Specific objectives of the Primary Study:
- To describe socio-demographic characteristics of people seeking HCV self-testing
- To evaluate preference for oral fluid or blood-based HCV self-tests
- To evaluate the proportion of people using home-based delivery vs pick up of HCV self-tests
- To evaluate the proportion of people reporting HCV self-test results
- To evaluate the proportion of people attending a consultation when HCV self-test is reactive or invalid
- To evaluate the knowledge of SGM about HCV infection and/or treatment
- To evaluate cost per case of HCV infection detected using HCV self-testing and internet technologies
- To evaluate the proportion of people with reactive HCVST who had HCV-RNA test for confirmation and who started HCV treatment (linkage to HCV continuum of care)
- To evaluate the proportion of people who ordered HCVST to receive an HIVST kit
Specific objectives of the Ancillary Study:
- To describe socio-demographic characteristics of people under PrEP performing HCVST
- To evaluate the proportion of people who correctly perform HCVST
- To evaluate the proportion of people who do not need assistance to correctly perform HCVST
- To evaluate the proportion of people who correctly report HCVST results (re-read by a trained healthcare worker)
- To evaluate the concordance of HCVST with re-testing by a trained healthcare worker
- To evaluate the preference for oral-fluid or blood-based HCVST kits
- To evaluate the proportion of people attending a consultation when HCV self-test is reactive or invalid
- To evaluate the knowledge of people under PrEP about HCV infection and/or treatment
- To evaluate cost per case of HCV infection detected using HCVST in PrEP users
- To evaluate the proportion of people with reactive HCVST who had HCV-RNA test for confirmation and who started HCV treatment (linkage to HCV continuum of care)
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Primary Study | – | Diagnostic Test: Hepatitis C virus self-test (oral fluid HCVST), Diagnostic Test: Hepatitis C virus self-test (blood-based HCVST)The study will be a cohort study. Adult SGM living in the metropolitan area of Rio de Janeiro who voluntary want to perform HCV testing ordered through a web-based platform will be eligible for this study. SGM will be defined by gay, bisexual and other cisgender MSM, TGW, transgender men, and gender nonbinary/diverse individuals. |
| Ancillary Study | – | Diagnostic Test: Hepatitis C virus self-test (oral fluid HCVST), Diagnostic Test: Hepatitis C virus self-test (blood-based HCVST)The study will be a cross-sectional study. Adult MSM or TGW attending a presential visit for PrEP (initiation or follow-up) at INI/FIOCRUZ will be eligible for this study. |
Who may qualify
- Ages
- 18 to 99 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Primary Study: Participants reported residence in the metropolitan area of Rio de Janeiro (municipalities of Rio de Janeiro, Duque de Caxias, São João de Meriti, Belford Roxo, Nilópolis, Mesquita, Nova Iguaçu, Queimados, Japeri, Paracambi, Seropédica, Itaguaí, Magé, Guapimirim, Niterói, São Gonçalo, Itaboraí, Seropédica, Rio Bonito, Tanguá and Maricá) Ancillary Study: 2. Self-identification as MSM or TGW 3. Presential visit for PrEP (initiation or follow-up) at INI/FIOCRUZ
Key inclusion criteria (3 listed)
- Age ≥ 18 years old with knowledge of the Portuguese language
- Self-identification as gay, bisexual and other cisgender MSM, TGW, transgender men, and gender nonbinary/diverse individuals
- Reported residence in the metropolitan area of Rio de Janeiro (municipalities of Rio de Janeiro, Duque de Caxias, São João de Meriti, Belford Roxo, Nilópolis, Mesquita, Nova Iguaçu, Queimados, Japeri, Paracambi, Seropédica, Itaguaí, Magé, Guapimirim, Niterói, São Gonçalo, Itaboraí, Seropédica, Rio Bonito, Tanguá and Maricá)
Key exclusion criteria (1 listed)
- 1. Unable or not willing to provide informed consent
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Hepatitis C virus self-test (oral fluid HCVST)Also: OraSure Technologies, Inc, Bethlehem, PAThe participant will be able to choose between oral-fluid or blood-based HCVST. The package will include an HCV OraQuick ® HCV Self-Test kit, (OraSure Technologies, Inc, Bethlehem, PA) or a Wondfo® HCV Self-Test (Guangzhou, P.R. China) at Primary Study. At Ancyllary study, the individuals attending PrEP consultations at INI/FIOCRUZ will be invited to perform HCVST using blood-based and oral-fluid kits. | Diagnostic test | Ancillary Study, Primary Study |
| Hepatitis C virus self-test (blood-based HCVST)Also: Wondfo® HCV Self-Test (Guangzhou, P.R. China)The participant will be able to choose between oral-fluid or blood-based HCVST. The package will include an HCV OraQuick ® HCV Self-Test kit, (OraSure Technologies, Inc, Bethlehem, PA) or a Wondfo® HCV Self-Test (Guangzhou, P.R. China) at Primary Study. At Ancylary Study, the individuals attending PrEP consultations at INI/FIOCRUZ will be invited to perform HCVST using blood-based and oral-fluid kits. | Diagnostic test | Ancillary Study, Primary Study |
Primary outcome
Number of SGM living in Rio de Janeiro (Brazil) who requested an HCVST kit through a web-based platform
Time frame: 1 month
Captured datas obtained from a web-based plataform
Number of SGM living in Rio de Janeiro (Brazil) who received and performed the test.
Time frame: 1 month
Captured datas obtained from a web-based plataform
Proportion of MSM/TGW who correctly performed HCVST with oral-fluid and blood-based kits without assistance of a healthcare worker
Time frame: 1 day
Captured datas obtained from a web-based plataform
18 secondary outcomes
Socio-demographic characteristics through the data obtained from the study.
Time frame: 2 months
Type-preference test through the data obtained from the study.
Time frame: 2 months
Participants who reported Easy test.
Time frame: 2 months
Possible outcomes through the data obtained from the study.
Time frame: 2 months
Participants through the data obtained from the study.
Time frame: 2 months
Participants who attending a consultation through the data obtained from the study.
Time frame: 2 months
Prevalence of reactive HCV through the data obtained from the study.
Time frame: 2 months
Cost per identification through the data obtained from the study.
Time frame: 2 months
Particiopants who used telehealth through the data obtained from the study.
Time frame: 2 months
Socio-demographic characteristics of MSM/TGW through the data obtained from the study.
Time frame: 1 month
Participants who report the test through the data obtained from the study.
Time frame: 1 month
Participants who needed help from a healthcare.
Time frame: 1 month
Preference for tests
Time frame: 1 month
Easy test
Time frame: 1 month
Participants who needed a consultation.
Time frame: 1 month
Positive participants
Time frame: 1 month
Cost for using the test
Time frame: 1 month
Positive participants with HCV-RNA
Time frame: 1 month
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Jan 2024.
- Individual participant dataSharing planned: No. There is a risk of loss of participant confidentiality and there is no authorization from the ethics committee to make individual data available. All data will be made available through scientific publications.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Hepatitis C, run by Oswaldo Cruz Foundation at 1 site in Brazil.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 12 Jan 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Brazil. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of SGM living in Rio de Janeiro (Brazil) who requested an HCVST kit through a web-based platform (time frame: 1 month). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Jan 2024.