A Chatbot to Reduce Chemsex and HIV-related Risk Behaviors Among Men Who Have Sex With Men

ConditionBehavior
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18+
SponsorChinese University of Hong Kong

About this trial

The goal of this clinical trial is to investigate whether receiving chatbot-delivered stage-of-change-tailored online interventions is effective in reducing chemsex among men who have sex with men in Hong Kong. The main question it aims to answer is:

Does chatbot-delivered stage-of-changed online interventions reduce chemsex among men who have sex with men

Eligible participants will be randomly assigned to either the intervention or the control group. The control group will watch one online video introducing chemsex-related knowledge and harm reduction skills per week for 12 weeks. On top of the interventions received by the control group, participants in the intervention group will have access to a chatbot during the 12-week intervention period. The chatbot will deliver 12 weekly episodes of interventions tailored to once's current stage-of-change related to chemsex. The chatbot will also address questions related to chemsex during the intervention period.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Hong Kong men aged at least 18 years

Able to understand Cantonese

Had anal intercourse with at least one man within the past six months

Willingness to provide contact information for follow-up

Disqualifiers

Self-reported a diagnosis of schizophrenia or bipolar disorder

Trial design

Design model

Parallel

Treatments tested in this trial

  • Chatbot-delivered online interventions and online videos

    Behavioral

    Participants will watch one online video introducing chemsex-related knowledge and harm reduction skills per week for 12 weeks. The chatbot will deliver 12 weekly episodes of interventions tailored to once's current stage-of-change related to chemsex. The chatbot will also address questions related to chemsex during the intervention period.

  • Online videos only

    Behavioral

    Participants will watch one online video introducing chemsex-related knowledge and harm reduction skills per week for 12 weeks.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Intervention groupExperimental treatment 1 intervention
Group B: Control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Presence of chemsex in the past 3 months

Presence of chemsex will be measured by a validated questionnaire. Chemsex is defined as the use of any of the following psychoactive substances before or during sexual intercourse: ketamine, methamphetamine, cocaine, cannabis, ecstasy, Dormicum/Halcion/Erimin 5/nonprescription hypnotic drugs, heroin, cough suppressant (not for curing cough), amyl nitrite (popper), GHB/GBL, 5-methoxy-N, N-diisopropyltryptamine (Foxy), and mephedrone. Participants will be asked whether they had used any of the aforementioned psychoactive substances before or during sexual intercourse in the past 3 months at baseline, after completion of the 12-week intervention (Month 3 or Week 12), and 3 months after completion of the 12-week intervention (Month 6)

Time frame
Baseline, after completion of the 12-week intervention (Month 3 or Week 12), and 3 months after completion of the 12-week intervention (Month 6)

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: