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

March 31, 2023 updated by: Zixin Wang, Chinese University of Hong Kong

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

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.

Study Overview

Study Type

Interventional

Enrollment (Anticipated)

244

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Hong Kong, Hong Kong, 666888
        • Recruiting
        • Centre for Health Behaviours Research, the Chinese University of Hong Kong
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: WeChat Mini Program plus tailored online promotion videos
  1. Having access to a WeChat Mini Program providing HIV and STI prevention information during the project period
  2. The WeChat Mini Program proactively asks questions assessing sexual risk behaviors at Month 0 and Month 1, and invite participants two watch online health promotion videos tailored to their sexual risk behaviors status.
Participants have access to a WeChat Mini Program. Participants will also watch online health promotion videos tailored to their current sexual behaviors.
Active Comparator: WeChat Mini Program Only
Having access to a WeChat Mini Program providing HIV and STI prevention information during the project period
Participants only have access to a WeChat Mini Program.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sexual intercourse with non-regular female sex partner
Time Frame: 6 months
Proportion of the participants who have sexual intercourse with a non-regular female sex partner in the past six months
6 months
Sexual intercourse with female sex workers
Time Frame: 6 months
Proportion of participants who have sexual intercourse with a female sex worker in the past six months
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Condomless sex with non-regular female sex partners
Time Frame: 6 months
Proportion of the participants who have condomless sex with a non-regular female sex partner in the past six months
6 months
Condomless sex with female sex workers
Time Frame: 6 months
Proportion of the participants who have condomless sex with a female sex worker in the past six months
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2021

Primary Completion (Anticipated)

April 30, 2023

Study Completion (Anticipated)

April 30, 2023

Study Registration Dates

First Submitted

March 20, 2023

First Submitted That Met QC Criteria

March 31, 2023

First Posted (Actual)

April 13, 2023

Study Record Updates

Last Update Posted (Actual)

April 13, 2023

Last Update Submitted That Met QC Criteria

March 31, 2023

Last Verified

March 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • HLPM201907020105

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

The data involve sensitive sexual behaviors of the participants

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Behavior, Sex

Clinical Trials on WeChat Mini Program plus tailored online health promotion videos

3
Subscribe