Exploring how lifestyle factors relate to cardiovascular health
Relationship Between Lifestyle Indicators (Healthy Behaviours) and Cardiovascular Clinical Parameters (Healthy Factors)
This study looks at how things like exercise, stress, and diet affect heart health in both adults and children.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 6 Years and up |
| Sex | All |
| Sponsor | Istituto Auxologico Italiano Academic / other |
| Locations | 1 site (Milan) |
| Trial ID | NCT06283069 on ClinicalTrials.gov |
What this trial studies
This observational study aims to create a comprehensive register by collecting data from questionnaires focused on lifestyle factors among adults and children. The investigators will analyze the correlations between lifestyle indicators, such as physical activity, stress levels, and diet quality, and various cardiovascular health parameters, including blood pressure and glucose-lipid profiles. By expanding their existing database, the study seeks to strengthen the understanding of how these lifestyle factors impact cardiovascular health outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study include adults and children who can provide informed consent and complete the lifestyle questionnaire.
Not a fit: Patients who are unable to fill in the questionnaire or provide informed consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into how lifestyle modifications can improve cardiovascular health.
How similar studies have performed: While similar studies have explored lifestyle factors and cardiovascular health, this specific approach of building a comprehensive register is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: \- ability to provide informed consent in compliance with the rules of Good Clinical Practice and current national regulations Exclusion Criteria: * inability to fill in the questionnaire * inability to provide informed consent * unwillingness to participate in the study
Where this trial is running
Milan
- Istituto Auxologico Italiano — Milan, Italy (Recruiting)
Study contacts
- Study coordinator: Luca Giovanelli, MD
- Email: luca.giovanelli@unimi.it
- Phone: +390261911
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.