MedPath

Perception of Cardiovascular Risk

Active, not recruiting
Conditions
Heart Diseases
Cardiovascular Diseases
Interventions
Other: Prevention events organized by participating centers
Registration Number
NCT06190743
Lead Sponsor
Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo di Alessandria
Brief Summary

The aim of the study is to describe the association between the perception of cardiovascular (CV) risk and the actual CV risk and, secondarily, to detect the actual CV risk to assess the prevalence of clinical risk factors, determined by means of appropriate instruments.

Detailed Description

Cardiovascular (CV) disease is the major cause of premature death in adults that carries serious economic consequences.

Risk perception for CV disease has been reported as the subjective judgment of the likelihood of having a CV event. Risk perception is an important precursor to adopting a healthy lifestyle. However, both overestimation and underestimation of actual risk due mostly to poor health literacy are common.

For these reasons, CV prevention services of health care professionals (e.g., nurses, physicians) should, on the one hand, include screening for the presence of risk factors, and on the other hand, know the CV risk perceptions of those being cared for.

The aim of the study is to describe the association between the perception of cardiovascular (CV) risk, investigated by means of the Perception of Risk of Heart Disease Scale and a Likert-5 scale question, and the actual CV risk according to the SCORE2 and, secondarily, to detect the actual CV risk ascertained by the SCORE2 and to assess the prevalence of clinical risk factors (alterations in the lipid, glucose, or anthropometric profile) determined by means of appropriate instruments.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
271
Inclusion Criteria
  • an age between 18 and 69 years of age
  • subscription to informed consent.
Exclusion Criteria
  • patients with a positive history of hospitalization due to CV pathology at the time of enrollment;
  • patients with ongoing relevant cognitive debilitation (Six Item Screener score < 4)

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Study GroupPrevention events organized by participating centersAdult individuals who voluntarily wish to participate in prevention events organized by participating centers
Primary Outcome Measures
NameTimeMethod
Duke-UNC Functional Social Support QuestionnaireScreening

Strength of affective support derived from people close to the enrolled subjects

Systemic Coronary Risk Estimation version2Screening

Individual real risk at 10 years, both for fatal CV events, and also for nonfatal CV events (myocardial infarction and stroke) in apparently healthy subjects

Patient Health Questionnaire-4Screening

Screening for the uptake of psychological symptoms of anxiety or depression in the primary care setting

Perception of Risk of Heart Disease ScaleScreening

Individual perception of the likelihood of having heart disease

Secondary Outcome Measures
NameTimeMethod
GlucoseScreening

Glucose measurement

Lipid panelScreening

Lipid panel measurement

HeightScreening

Height measurement

WeightScreening

Weight measurement

Trial Locations

Locations (1)

Azienda Ospedaliera SS Antonio e Biagio e Cesare Arrigo

🇮🇹

Alessandria, Piedmont, Italy

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