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Crowdsourcing to Promote HBV and HCV Testing in China

A Crowdsourced Intervention to Promote Hepatitis B and C Testing Among Men Who Have Sex With Men in China: a Nationwide Online Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03482388
Enrollment
700
Registered
2018-03-29
Start date
2018-05-09
Completion date
2018-06-09
Last updated
2018-06-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatitis, Hepatitis B, Hepatitis C

Keywords

Hepatitis, Hepatitis B, Hepatitis C, Men who have sex with men, Crowdsourcing, China, Testing

Brief summary

This is an online randomized controlled trial (RCT) comparing men who have sex with men (MSM) exposed to a crowdsourced intervention to MSM who did not receive the intervention to determine the effect on Hepatitis B Virus (HBV) and Hepatitis C Virus (HCV) testing. Participants will be randomly assigned in a 1:1 ratio to intervention or control using a computer-based allocation system. Participants will be assessed for primary and secondary outcomes four weeks after randomization.

Detailed description

700 MSM will be recruited through social media operated by gay organizations in China. Eligible participants will be born biologically male, age 16 years or older, report previous anal sex with another man, and reside in China. Men self-reporting previous HBV vaccination, HBV testing, or HCV testing will be excluded. After completing a baseline online survey, participants will be randomly assigned to intervention or control arms with a 1:1 allocation ratio. The intervention will include two components: (1) a multimedia component will deliver two videos and two images promoting HBV and HCV testing developed through a crowdsourcing contest in China. (2) A participatory component will invite men to submit suggestions for how to improve crowdsourced videos and images. The control arm will not view any images or videos and will not be invited to submit suggestions. All participants will be offered reimbursement for HBV and HCV testing costs. The primary outcome is HBV and HCV test uptake confirmed through electronic submission of test report photos within four weeks of enrollment. Secondary outcomes include self-reported HBV and HCV test uptake, HBV vaccination uptake, and change in stigma toward people living with HBV measured through a follow-up survey after four weeks. Men with primary and secondary outcomes will be calculated using intention to treat and as-exposed analyses and compared using two-sided 95% confidence intervals.

Interventions

BEHAVIORALCrowdsourced materials

Among participants randomized to the intervention arm, intervention images and videos promoting HBV and HCV testing will be delivered through the WeChat platform. Men will also be invited to submit suggestions for how to improve intervention videos and images.

OTHERControl

Participants will not view any images or videos promoting HBV and HCV testing.

Sponsors

Doris Duke Charitable Foundation
CollaboratorOTHER
University of North Carolina, Chapel Hill
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
NONE

Intervention model description

Participants will be randomly assigned in a 1:1 ratio to the study intervention or control

Eligibility

Sex/Gender
MALE
Age
16 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 16 years of age or older * male * report having had anal sex with another man at least once in the past * currently reside in China * willing to provide working mobile phone number and WeChat account

Exclusion criteria

* previous HBV vaccination * previous HBV testing * previous HCV testing

Design outcomes

Primary

MeasureTime frameDescription
Confirmed HBV and HCV test uptakeenrollment - 4 weeks after enrollmentDefined as frequency of men who had both HBsAg test uptake and anti-HCV IgG test uptake confirmed through electronic submission of a test report photo showing serology results, age of tester, sex of tester, and date of test

Secondary

MeasureTime frameDescription
Self-reported HCV test uptakeenrollment - 4 weeks after enrollmentDefined as frequency of men who had anti-HCV IgG uptake within four weeks of enrollment, self-reported in follow-up survey
HBV vaccination uptakeenrollment - 4 weeks after enrollmentDefined as frequency of men who had receipt of at least a one dose of the HBV vaccine within four weeks of enrollment, self-reported in follow-up survey
Confirmed HBV test uptakeenrollment - 4 weeks after enrollmentDefined as frequency of men who had HBsAg test uptake through electronic submission of a test report photo showing serology results, age of tester, sex of tester, and date of test
Confirmed HCV test uptakeenrollment - 4 weeks after enrollmentDefined as frequency of men who had anti-HCV IgG test uptake confirmed through electronic submission of a test report photo showing serology results, age of tester, sex of tester, and date of test
HBV vaccination uptake among men with confirmed susceptibility to HBV infectionenrollment - 4 weeks after enrollmentDefined as frequency of men with negative HBsAg and negative anti-HBs results confirmed through electronic submission of a test report photo showing serology results, who had receipt of at least a one dose of the HBV vaccine within four weeks of enrollment, self-reported in follow-up survey
Self-reported HBV test uptakeenrollment - 4 weeks after enrollmentDefined as frequency of men who had HBsAg uptake within four weeks of enrollment, self-reported in follow-up survey
Chlamydia test uptakebaseline - 4 weeks after enrollmentDefined as frequency of men who had chlamydia test uptake within four weeks of enrollment, self-reported in follow-up survey
Gonorrhea test uptakeenrollment - 4 weeks after enrollmentDefined as frequency of men who had gonorrhea test uptake within four weeks of enrollment, self-reported in follow-up survey
Syphilis test uptakeenrollment - 4 weeks after enrollmentDefined as frequency of men who had syphilis test uptake within four weeks of enrollment, self-reported in follow-up survey
Change in stigma toward people living with HBVenrollment - 4 weeks after enrollmentContinuous variable, defined as difference between Toronto Chinese HBV Stigma Scale score assessed at follow-up and baseline. Stigma toward people living with HBV will be measured at baseline and follow-up using 20 survey items that are each on a five point Likert scale. The 20 items were originally developed as the Toronto Chinese HBV Stigma Scale (potential range of 20 - 100), which has been previously validated and correlated to HBV testing behaviors among Chinese populations. Decreased stigma toward people living with HBV will be defined as a mean composite score that is less at follow-up compared to baseline.
Visit with a physician after hepatitis test uptakeenrollment - 4 weeks after enrollmentDefined as frequency of men who had HBV and/or HCV test uptake and saw a physician to discuss hepatitis test results within four weeks of enrollment, self-reported in follow-up survey
HIV test uptakeenrollment - 4 weeks after enrollmentDefined as frequency of men who had HIV test uptake within four weeks of enrollment, self-reported in follow-up survey

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026