RecruitingNANCT07612852

Digital Engagement for Lifelong Prevention and Health Improvement

Sponsor: Istituto per la Ricerca e l'Innovazione Biomedica

Trial Details

ConditionLife Style, Healthy, Risk Reduction, Health Promotion
InterventionDELPHI Personalized Digital Prevention Platform; Passive Digital Monitoring Control
PhaseNA
StatusRecruiting
Participants200
Est. Completion30 Nov 2026
Last Updated29 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

Italy
View Registry Entry

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