- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05811611
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
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
Status
Conditions
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Zixin Wang, PhD
- Phone Number: +852 22528740
- Email: wangzx@cuhk.edu.hk
Study Locations
-
-
-
Hong Kong, Hong Kong, 666888
- Recruiting
- Centre for Health Behaviours Research, the Chinese University of Hong Kong
-
Contact:
- Zixin Wang, PhD
- Phone Number: +852 22528740
- Email: wangzx@cuhk.edu.hk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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
|
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
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
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