Feasibility of Innovative Approaches for Personalized Cardiovascular Prevention

Recruiting now · Not applicable

Conditions studied: Coronary Heart Disease

In brief

The goal of the FITPREV (Feasibility of InnovaTive approaches for personalized cardiovascular PREVention: randomized controlled pilot trial and multidisciplinary evaluation for National Health Service implementation) clinical trial is to study the feasibility of innovative approaches( Polygenic Risk Score and health smartwatch) for personalized primary preventive interventions in cardiovascular diseases (CVD). The main questions it aims to answer are: * Feasibility of a greater study. * Feasibility of the interventions in a realistic setting, such as the medical office of a General Practitioner. Participants will be randomized in one of the four parallel arms: * standard of care; * genetic testing for cardiovascular genetic risk (through the cardiovascular Polygenic Risk Score or PRS); * digital intervention with a wearable device and its app; * digital intervention and genetic testing The primary outcomes that are going to be evaluated are patient's and General Practitioners' overall judgment of the study and its feasibility. Secondarily the efficacy of returning Polygenic Risk Score (PRS) results will be assessed. This will happen on two endpoints: i) change in lifestyle pattern; ii) CVD risk profile modification. The postulated hypothesis is that the achievement of these endpoints is more likely in presence of at least one of the aforementioned interventions than among subjects who receive only traditional risk assessment at baseline.

Key facts

Study ID: NCT06911294
Run by: Catholic University of the Sacred Heart
People needed: 120
Starts: 2025-02-10
Expected to finish: 2026-09-10
Last updated by the study team: 2025-08-05

Who can join

Age: 40 and older, up to 69. Sex: any. Healthy volunteers: accepted.

You may qualify if…

Age 40-69 years;
10 year cardiovascular risk score SCORE2 between 2.5% and 10%.
Diagnosis of metabolic syndrome according to the American Heart Association criteria , defined as the presence of three or more of the following:
Central or abdominal obesity, measured by waist circumference (greater than 40 inches - 102 cm in men and 35 inches - 89 cm in women).
Elevated triglycerides: levels equal to or greater than 150 mg/dL or use of medication for hypertriglyceridemia.
Low HDL cholesterol levels (less than 40 mg/dL in men and less than 50 mg/dL in women) or use of cholesterol-lowering medication.
Elevated blood pressure: systolic ≥130 mmHg or diastolic ≥85 mmHg, or use of antihypertensive medication.
Elevated fasting blood glucose: ≥100 mg/dL or use of glucose-lowering medication.

You may not qualify if…

Diabetes:
Familial hypercholesterolemia;
Previous cardiovascular events.

Where it is running

Studio Antonaci — Rome, Italy, Italy (enrolling)
Studio Colletti — Rome, Italy (enrolling)
Studio Maggiori — Rome, Italy (enrolling)
Studio Mammucari — Rome, Italy (enrolling)
Studio Marra — Rome, Italy (enrolling)
Studio Paoletti — Rome, Italy (enrolling)
Studio Pasca — Rome, Italy (enrolling)

Full record on ClinicalTrials.gov

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