Digital Engagement for Lifelong Prevention and Health Improvement
Sponsor: Istituto per la Ricerca e l'Innovazione Biomedica
Trial Details
| Condition | Life Style, Healthy, Risk Reduction, Health Promotion |
| Intervention | DELPHI Personalized Digital Prevention Platform; Passive Digital Monitoring Control |
| Phase | NA |
| Status | Recruiting |
| Participants | 200 |
| Est. Completion | 30 Nov 2026 |
| Last Updated | 29 May 2026 |
Primary Outcome
World Health Organization Quality of Life (WHOQoL); Depression, Anxiety, and Stress Symptoms (DASS-21); Beck Depression Inventory-II (BDI-II); International Physical Activity Levels (IPAQ); Prevention with Mediterranean Diet (PREDIMED)
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: * Apparent good general health status, confirmed by medical history and initial self-assessment. * Ability to understand the study information and provide informed consent. * Availability and motivation to participate for the entire duration of the study (12 months). * Access to a smartphone compatible with the DELPHI application. * Willingness to wear the wearable devices for continuous monitoring of physiological parameters. * Basic familiarity with mobile applications or willingness to receive training on their use. * Signed informed consent. Exclusion Criteria: * Presence of severe chronic diseases in active phase (e.g., oncological, cardiovascular, or neurological diseases). * Acute or unstable conditions that could compromise participation in the protocol. * Current pregnancy. * Diagnosed major cognitive or psychiatric disorders that hinder understanding of or adherence to the protocol. * Current use of medications that significantly affect the parameters being monitored (e.g., psychotropic drugs, beta-blockers). * Simultaneous participation in other clinical studies. * Logistical difficulties that prevent frequent interaction with the platform (e.g., lack of connection, unwillingness to attend periodic follow-ups).
Trial Sites
Countries
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