Effects, Acceptability, and Use of a Dynamically Tailored Mobile What Do You Drink Intervention to Reduce Excessive Drinking Among Adolescents and Young Adults in the Netherlands: Randomized Controlled Trial
Clinical Snapshot
PICO Framework
| P — Population | Adolescents and young adults (median age 19.4 years) at risk for excessive alcohol consumption in the Netherlands |
| I — Intervention | What Do You Drink (WDYD) - a 17-week dynamically tailored mobile health app providing personalized feedback sessions and goal-monitoring reminders |
| C — Comparator | Control group receiving no tailored intervention sessions |
| O — Outcomes | Primary: excessive drinking, binge drinking, weekly alcohol consumption. Secondary: intrinsic motivation, self-confidence, mood, acceptability and app usage |
Bottom Line
This large Dutch RCT of a mobile alcohol intervention for young people demonstrates the challenges of sustaining engagement in digital health interventions. While the 'What Do You Drink' app showed initial promise with modest reductions in excessive drinking at week 1 and improvements in motivation and self-confidence, the catastrophic 96% dropout rate by study end severely limits clinical utility. The lack of sustained effects on primary drinking outcomes, combined with methodological limitations including absence of blinding and unclear baseline comparability, suggests this intervention model is not ready for clinical implementation. The findings highlight the critical need for better engagement strategies in digital health interventions for young people. Australian clinicians should focus on evidence-based brief interventions with demonstrated retention and effectiveness rather than resource-intensive mobile apps with poor engagement profiles.
Key Findings
P Value: Not explicitly reported for primary outcomes
Effect Size: Week 1 excessive drinking: standardized β=-0.35; binge drinking: standardized β=-0.36
Primary Outcome: No significant reduction in excessive drinking, binge drinking, or weekly alcohol consumption except at week 1
Nnt Or Sensitivity: Cannot be calculated due to lack of significant sustained effects on primary outcomes
Confidence Interval: Excessive drinking: 95% CI -0.64 to -0.05; binge drinking: 95% CI -0.68 to -0.04
Clinical Application
Poor feasibility demonstrated by 96% dropout rate. Requires substantial resources for minimal sustained benefit Limited relevance to Australian practice. Different drinking culture and healthcare system. Would require adaptation and likely face similar engagement challenges Limited applicability due to high dropout rates. May only be suitable for highly motivated adolescents and young adults willing to engage long-term
Abstract
BACKGROUND: Excessive alcohol consumption among adolescents and young adults is a serious health problem. Dynamically tailored interventions could reduce their excessive drinking. We therefore developed "What Do You Drink" (WDYD), a 17-week dynamically tailored mHealth (mobile health) intervention providing personalized support on alcohol consumption. OBJECTIVE: We aim to evaluate the effectiveness, acceptability, and use of WDYD in reducing alcohol consumption of adolescents and young adults at risk. METHODS: We conducted a 2-arm, parallel-group randomized controlled trial using ecological momentary assessments. Recruitment was via an educational alcohol program, an online lifestyle monitor, social media advertisements, or news items on websites. Participants downloaded the standalone WDYD app, and when having given active informed consent, were randomized to the intervention or control group. Participants in the intervention group received dynamically tailored feedback sessions on alcohol consumption (wk 0-5, 7, 9, 13, and 17) and goal-monitoring reminders. Both groups completed an online baseline survey, 2 follow-up surveys (wk 9 and 33), and various ecological momentary assessments (7 daily assessments during wk 1, 7, 13, 19, 25, 31, and 33). Participants provided consent before randomization, in which they were informed that 2 study groups existed. After randomization, no disclosure of group assignment was provided, although participants could potentially infer it from receiving tailored sessions vs no tailored sessions. Primary outcomes were excessive drinking, binge drinking, and weekly alcohol consumption. Secondary outcomes were intrinsic motivation, self-confidence, and mood. Acceptability of WDYD was measured by survey questions; use was tracked via app data logs. RESULTS: Analyses were based on data from 1767 participants; 720 in the intervention group and 1047 participants in the control group. Almost half of them were female (2276/4795, 47.5%), and most (3471/4595, 72.4%) participants were aged 18-24 (median 19.40, IQR 2.92) years. The dropout rate was high, up to 96% (4603/4795) in the final 33rd week. No significant effect of WDYD was found on primary outcomes and mood, except for week 1 (excessive drinking: standardized β=-0.35, SE 0.15; 95% CI -0.64 to -0.05; binge drinking: standardized β=-0.36, SE 0.16; 95% CI -0.68 to -0.04; mood: standardized β=0.20, SE 0.06, 95% CI 0.08 to 0.32). Both groups reduced their alcohol consumption. Significant positive effects were found for intrinsic motivation and self-confidence up to 25 weeks (wk 25: standardized β=0.54, SE 0.24; 95% CI 0.06 to 1.02 for motivation; standardized β=0.72, SE 0.26; 95% CI 0.22 to 1.23 for self-confidence). Participants evaluated WDYD as acceptable and usable. CONCLUSIONS: WDYD did not significantly reduce excessive drinking compared to control, but improved motivation and self-confidence. High dropout rates highlight challenges in sustaining engagement in long-term mHealth interventions. Future research should explore strategies to enhance retention and optimize dynamic tailoring.
References
- 1.van Keulen, H., Voogt, C., Kleinjan, M., Huizing, A., Andree, R., & van Empelen, P. (2026). Effects, Acceptability, and Use of a Dynamically Tailored Mobile What Do You Drink Intervention to Reduce Excessive Drinking Among Adolescents and Young Adults in the Netherlands: Randomized Controlled Trial. JMIR mHealth and uHealth. https://doi.org/10.2196/68468
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