Intervention Group: Healthy Lifestyle Recommender Solution (HLRS) will be developed as intervention tool for the trials. It integrates tools (mostly digital): a meal recommender to propose balanced and individually adapted meal plans, physical activity and sleep pattern measures and recommendations, assessment of behavioural/psychological aspects, and motivational features for sustained engagement and adherence. Within our multi-disciplinary portfolio approach, a set of predominantly eHealth solutions applied during the intervention trials for overweight/obesity prevention, developed in a participatory design approach with relevant stakeholders. This will include the HLRS, thus combining motivational features (nudging, gamification), targeted psychological support, dietary and physical activity advice, though also additional recommendations (healthy eating guidelines...) or education materials will be provided. Intervention trials/studies.
The goal of the HealthyW8 study (an intervention study) is:
To assess the usefulness and effects of a digital-based healthy lifestyle recommender system (HRLS) on the prevention of obesity in the following propulations: schoolchildren (5-10 y) and their parents, young adults (18-25 y) and elders (\>65 y).
The main questions it aims to answer are:
Outcome 1: To select and validate a tool-assisted 3-mo intervention (mostly digital) by iteratively testing the HLRS on reducing risk of overweight/obesity among the described age groups.
Outcome 2: To assess the effect of 1-y interventions (mostly digital) with the HLRS described and further iteratively improved previously (outcome 1) on reducing risk of overweight/obesity at described ages.
Researchers will compare the intervention group before the intervention (baseline) and after it (3-mo intervention trial), or control group (standard care) vs. Intervention group (1-y intervention) to see changes on changes in overweight/obesity, and related parameters (body composition and biomarkers).
Participants will follow the HLRS recommendations (meal plans, physical activity and sleep pattern measures and recommendations, assessment of behavioural/psychological aspects, and motivational features through digital devices), which will be assessed by means of measurement of body weight, body composition, and biomarkers.
| Facility | City | Region | Status |
|---|---|---|---|
| Virtech Ood | Sofia | Bulgaria | |
| Regional Cluster North-East | Varna | Bulgaria | |
| Danmarks Tekniske Universitet | Kongens Lyngby | Denmark | |
| Leibniz-Institut Fur Praventionsforschung Und Epidemiologie - Bips Gmbh | Bremen | Germany | |
| Deutsches Forschungszentrum Fur Kunstliche Intelligenz Gmbh | Kaiserslautern | Germany | |
| Universita Degli Studi Di Scienze Gastronomiche | Bra | Italy | |
| Luxembourg Institute of Health | Luxembourg | Luxembourg | |
| Technische Universiteit Eindhoven | Eindhoven | Netherlands | |
| Universidade de Coimbra | Coimbra | Portugal | |
| Universidade de Evora | Evora | Portugal | |
| Fundacio Institut D'Investigacio Sanitaria Illes Balears (Idisba) | Palma de Mallorca | Balearic Islands | |
| Centre de Recerca En Economia I Desenvolupament Agroalimentari-Upc-Irta | Castelldefels | Spain | |
| Centro de Investigacion Y Tecnologia Agroalimentaria de Aragon | Zaragoza | Spain |
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07011368 on ClinicalTrials.gov ↗ ← All trials in Germany