Actively Recruiting

Phase Not Applicable
Age: 40Years +
All Genders
Healthy Volunteers
NCT06888466

Personalised HeartCare: Poligenic Risk Scores Disclosure for Cardiovascular Prevention

Led by Catholic University of the Sacred Heart · Updated on 2026-02-20

650

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to evaluate whether the disclosure of Polygenic Risk Scores (PRS) combined with personalized coaching on risk factors can lead to significant improvements in lifestyle behaviors among staff members at Fondazione Policlinico Universitario Agostino Gemelli IRCCS. The study includes staff members from Fondazione Policlinico Universitario Agostino Gemelli IRCCS, enrolled at the outpatient clinics of the Cardiology Department. Main Research Questions: 1. Does receiving PRS disclosure and personalized coaching lead to significant improvements in lifestyle behaviors compared to baseline measurements? 2. How do different levels of genetic predisposition to cardiovascular diseases (CVD) impact behavioral changes following intervention? This is a single arm, pre-post clinical trial. Participant will: * Undergo genetic testing to assess their Polygenic Risk Score for CVDs * receive personalized, in-person consultation with a medical cardiologis, together with and individualized recommendations for CVD prevention based on PRS results and traditional risk factors.

CONDITIONS

Official Title

Personalised HeartCare: Poligenic Risk Scores Disclosure for Cardiovascular Prevention

Who Can Participate

Age: 40Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Traditional cardiovascular risk assessed using SCORE 2 or SCORE 2-OP with low to moderate risk levels
  • Blood tests performed within the past 6 months
  • Age of 40 years or older
Not Eligible

You will not qualify if you...

  • Very high cardiovascular risk as measured by SCORE 2 or SCORE 2-OP
  • Diagnosis of diabetes
  • Familial hypercholesterolemia
  • Previous cardiovascular events or established cardiovascular disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Dipartimento Universitario di Scienze della Vita e Sanità Pubblica

Roma, Italia, Italy, 00168

Actively Recruiting

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Research Team

S

Stefania Boccia

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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