NCT06983431Recruiting
DIGITALIZATION OF PERSONALISED HEALTH RISK MANAGEMENT
DIGITALIZATION OF PERSONALISED HEALTH RISK MANAGEMENT IN AT-RISK GROUPS TO IMPROVE HEALTH OUTCOMES THROUGH INTEGRATION OF TECHNOLOGICAL AND SOCIAL INNOVATION
Source: ClinicalTrials.gov · Last updated 21 May 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 320 (estimated)
- First submitted
- 29 Apr 2025
- Start date
- 5 May 2025
- Primary completion date
- 5 May 2026
- Lead sponsor
- Slovak Academy of Sciences
- Diseases
- Obesity
- NCT number
- NCT06983431
What you commit to
- Study type: Interventional
- Planned participants: 320
- From 5 May 2025 to the primary completion date, 5 May 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- patients using anti-obesity medications who are in the dosage adjustment phase within the last four weeks
Other illness
- diseases that prevent participation in the program, or insufficiently controlled diseases, or terminal-stage illnesses
- excessive alcohol consumption or a history of other addictions
Other
- patients currently participating in a weight-loss program (commercial, medically supervised, or a research study)
- patients who are not mentally, physically, or technologically capable of participating
- patients who are unable to provide informed consent
- patients not adhering to the study protocol
Who the study is looking for
- obesity (BMI 27-42 kg/m²)
- capacity and willingness to use smartphone
- capacity and willingness to use wearables
- readiness to change (validated questionaire)
Age in the registry: 25 years to 65 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Center for Obesity Management EASO, Biomedical Research Center SAS Coordinator of this site? Confirm its status | Bratislava | Slovakia | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.