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Two WeChat Mini Program-based Interventions Reducing Sexual Risk Behaviors Among Heterosexual Male Factory Workers

Efficacies of Two WeChat Mini Program-based Interventions in Reducing Sexual Risk Behaviors Among Heterosexual Male Factory Workers in China: a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05811611
Enrollment
244
Registered
2023-04-13
Start date
2021-12-01
Completion date
2023-04-30
Last updated
2023-04-13

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

Conditions

Behavior, Sex

Brief summary

A non-blinded parallel group randomized controlled trial is conducted. Adult male full-time employees of factories in Shenzhen who have access to smartphone and WeChat are recruited by staff of the Longhua Center for Disease Control and Prevention (CDC). After completing an online baseline questionnaire, participants will be randomized evenly to either the intervention group or the control group. Participants in the control group will have access to a WeChat Mini Program providing HIV and sexually transmitted prevention information during the project period. In addition to those received by the control group, the Mini Program will proactively ask participants in the intervention group some simple questions to assess presence of sexual risk behaviors at Month 0 and Month 1, and invite them to watch online health promotion video(s) tailored to their current sexual risk behaviors. All participants will complete two online follow-up surveys six and twelve months after completion of the interventions.

Interventions

BEHAVIORALWeChat Mini Program plus tailored online health promotion videos

Participants have access to a WeChat Mini Program. Participants will also watch online health promotion videos tailored to their current sexual behaviors.

BEHAVIORALWeChat Mini Program Only

Participants only have access to a WeChat Mini Program.

Sponsors

Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male at birth * Aged 18 years or above * Full-time employee of a factory in Shenzhen * Having a smartphone with internet access * Having installed or willing to install WeChat on the smartphone * Willing to complete follow-up surveys at Month 6 and 12

Exclusion criteria

* Oral or anal sex with a man * Blindness ot deafness * Not able to communicate effectively with project staff * Self-reported as HIV positive

Design outcomes

Primary

MeasureTime frameDescription
Sexual intercourse with non-regular female sex partner6 monthsProportion of the participants who have sexual intercourse with a non-regular female sex partner in the past six months
Sexual intercourse with female sex workers6 monthsProportion of participants who have sexual intercourse with a female sex worker in the past six months

Secondary

MeasureTime frameDescription
Condomless sex with non-regular female sex partners6 monthsProportion of the participants who have condomless sex with a non-regular female sex partner in the past six months
Condomless sex with female sex workers6 monthsProportion of the participants who have condomless sex with a female sex worker in the past six months

Countries

Hong Kong

Contacts

Primary ContactZixin Wang, PhD
wangzx@cuhk.edu.hk+852 22528740

Outcome results

None listed

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