DIGITALIZATION OF PERSONALISED HEALTH RISK MANAGEMENT

Summary

The principal objective of the project is:

* to bring together academic and business research organisations in a joint partnership integrating technological and social innovation,
* in order to develop proof-of-concept of a scalable and cost effective personalised digital health program for (pre)obesity patients,
* by integrating, in an ethical manner, adaptive AI components aimed at personalisation of the program as well as its cost management,
* with the ultimate objective to support sustained behavioural change leading to adoption and internalisation of healthy lifestyle choices.

Conditions

• Pre-obesity
• Obesity

Interventions

BEHAVIORAL

technology driven self coaching

subject will be provided with the technology driven lifestyle coaching based on the real time data from the wearables

BEHAVIORAL

Health coaching

participants will be provided with the health coach (expert) driven lifestyle coaching based on the real-time data from the wearables

BEHAVIORAL

Peer coaching

participants will be provided with the peer coach (expert) driven lifestyle coaching based on the real-time data from the wearables

BEHAVIORAL

Active Control

participants will be provided with the wearable, but not exposed to any of the coaching strategies. Real-time data provided by the wearable will be available to them.

Sponsors & Collaborators

• University Hospital Bratislava Comenius University

  collaborator UNKNOWN

• Kempelen Institute of Inteligent Technologies

  collaborator UNKNOWN

• Slovak Academy of Sciences

  lead OTHER_GOV

Principal Investigators

• Jozef Ukropec, PhD, DSc · Biomedical Research Center Slovak Acad Sci

• Zuzana Košutzka, A/prof., PhD · University Hospital Bratislava and Faculty of Medicine Comenius University

• Emília Sičáková - Beblavá, Prof. Ing. PhD · University Hospital Bratislava and Faculty of Medicine Comenius University

• Miroslav Beblavý, A/prof. PhD · University Hospital Bratislava and Faculty of Medicine Comenius University

Study Design

Allocation

RANDOMIZED

Purpose

HEALTH_SERVICES_RESEARCH

Masking

DOUBLE

Model

PARALLEL

Eligibility

Min Age

25 Years

Max Age

65 Years

Sex

ALL

Healthy Volunteers

No

Timeline & Regulatory

Start

2025-05-05

Primary Completion

2026-05-05

Completion

2026-06-30

Countries

• Slovakia

Study Locations