Relationship Between Lifestyle Indicators and Cardiovascular Clinical Parameters
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: compilation of a questionnaire about LifeStyle.
- Who it may be relevant to
- Registry conditions: Cardiovascular Diseases, Lifestyle, Nutrition, Healthy, Physical Inactivity. Basic parameters: from 6 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Italy
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Relationship Between Lifestyle Indicators (Healthy Behaviours) and Cardiovascular Clinical Parameters (Healthy Factors)
Overview
The goal of the study is to build a Register accruing data derived from the compilation of the questionnaire about LifeStyle for a population both of adults and of young boys and girls. The investigators are confident that in this way they will be able to expand the database they already have. The investigators will be able to increase the strength of the correlations between LS indices and health indicators. In particular, the investigators will emphasize the relationship between physical activity, stress, and diet quality on one hand, and on the other, they will focus on physiological parameters, like arterial pressure, gluco-lipid profile, and possible pathologies.
Interventions
- Behavioral compilation of a questionnaire about LifeStyle
compilation of a questionnaire about LifeStyle
Primary outcome measures
- weekly physical activity volume [Time frame: through study completion, an average of 1 year]
Secondary outcome measures (10)
- nutrition quality [Time frame: through study completion, an average of 1 year]
- weight [Time frame: through study completion, an average of 1 year]
- height [Time frame: through study completion, an average of 1 year]
- blood pressure [Time frame: through study completion, an average of 1 year]
- perception of stress, fatigue, and somatic symptoms [Time frame: through study completion, an average of 1 year]
- glycemia [Time frame: through study completion, an average of 1 year]
- cholesterol [Time frame: through study completion, an average of 1 year]
- creatinine [Time frame: through study completion, an average of 1 year]
- waist circumference [Time frame: through study completion, an average of 1 year]
- heart rate [Time frame: through study completion, an average of 1 year]
Eligibility 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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Other
Study locations
Italy · 1 center
- Istituto Auxologico Italiano — Milan
Identifiers
NCT: NCT06283069 · 45C301