An interventional study of Online platform hub and mHealth Text Messaging and Self-help material in Teen Drinking, sponsored by The University of Hong Kong. Recruiting at 2 sites in Hong Kong. Open to participants aged 12 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-05.
Sponsored by The University of Hong Kong · Not applicable, Interventional, and Prevention
Online education hubs and Chat-based text messaging for reducing alcohol consumption and binge drinking in adolescents: A pilot randomized controlled trial
It is urged to alleviate the problem before it become worse. Department of Health in Hong Kong developed 3 information hubs (Alcohol Fails, Young and Alcohol Free and Understanding Alcohol Harm) to distribute alcohol-related messages, such as binge drinking. Yet, it lacks interactive and individualized elements, which makes it difficult to attract secondary school students to search for information. Our previous research also reveals that more than 80% of the respondents are willing to receive message reminders for controlling or avoiding binge drinking. They also suggest that those messages should include drinking limits, health risks, psychological support, and alternative activities. It proves that an interactive and personalized intervention package should be included in secondary school in terms of binge drinking prevention. This could be a research gap to investigate in this project.
We expect that this study result would demonstrate the main effects of the interventions, including mHealth text messaging, and online platform hub. By analyzing those intervention results, we could deeply understand the effective methods to lower the risk of young adult binge drinking phenomenon. We could provide more precise interventions to secondary school students. This study will also prepare for future RCTs to explore the possibility on the integration of other intervention components or factors for binge drinking prevention research. In the long run, the proportion of binge drinking in population and young-aged will be lowered. Department of Health or other future research could implement this intervention as a fundamental to enhance the effectiveness of the alcohol control intervention.
A pilot 2-arm, parallel, open-labelled randomized controlled trial randomly allocated participants (1:1 ratio) to intervention and control groups. The intervention group has 2 intervention components: (1) Online information hub (compulsory: game), (2) mHealth text messaging at last to people who needed (Audit score >7). The control group will receive self-help materials during the same period. The sample size is 100 participants (50 for each group).
100 ever-drinkers will be recruited from the secondary schools through online and offline. Study information will be disseminated via online advertisements, mass emails, and in-person interactions at schools in various districts, including New Territories, Kowloon, and Hong Kong Island. Interested participants can enroll by completing an online application form using Qualtrics or Google form).
During offline recruitment sessions, staff will approach secondary school students and their parents (if the participants are under 18 years old) to obtain consent and have them complete a baseline questionnaire for further contact and intervention delivery.
44 studies on the registry are indexed under Underage Drinking; 13 are open to participants now.
This study's planned enrollment of 100 is below the median of 360 across 43 interventional studies indexed under Underage Drinking.
Browse Underage Drinking studies →The University of Hong Kong is the lead sponsor of 1,292 studies on the registry; 348 are open to participants now.
Of its 9 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.
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Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
The treatment package includes both optional and mandatory treatments. The mandatory treatments consist of mHealth text messaging and an online platform hub.
Behavioral: Online platform hub and mHealth Text Messaging
The control group will be provided a self-help material like leaflet for alcohol reduction, which involves education on alcohol harm and strategies for alcohol reduction.
Behavioral: Self-help material
The treatment package includes both optional and mandatory treatments. The mandatory treatments consist of mHealth text messaging and an online platform hub. We have developed a game which educates teenagers about alcohol reduction and promotes awareness of alcohol-related harm. Designed to be both engaging and informative, the game uses real-life scenarios, interactive storytelling, and decision-based gameplay to help young people understand the risks of excessive drinking. Also, participants with Audit Score \> 7 will receive individualized chat-based instant text messages from WhatsApp for 8 weeks. They will have real-time and one-to-one interaction. The conversation intensity depends on the participants' need.
Self-help material like leaflet is a common method used in preventing teenage Drinking.
Number of drinking days
The primary outcome is the number of drinking days in the past 30 days at 3-month follow-up.
Time frame: 3-month follow-up
Number of ever binge drinking days
Number of ever binge drinking days in the past 3 months at 3-month follow-up since trial participation
Time frame: 3-month follow-up
Number of binge drinking days
Number of binge drinking days in the past 30 days at 3-month
Time frame: 3-month follow-up
Intention to reduce or quit alcohol drinking
Intention to reduce or quit alcohol drinking in 10 points Likert scale at 3-month follow-up. \[0: no intention \| 10: Highest Intention\]
Time frame: 3-month follow-up
Alcohol Use Disorder Identification Test
Alcohol Use Disorder Identification Test (AUDIT) score is a validated scale in measuring the impact of alcohol consumption on individual's health.
Time frame: 3-month follow-up
Plan to share: Yes — Research data and documentation will be available upon request
Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Clinical study report, Analytic code
Time frame: 3 years after the completion of the relevant publications
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