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New Cardiovascular Risk Screening Strategy. (HELENA)

Primary Purpose

Cardiovascular Prevention, Screening, Peripheral Artery Disease

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
HELENA
Sponsored by
Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cardiovascular Prevention

Eligibility Criteria

50 Years - 74 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients aged 50 to 74, which are free or do not have previous history of CVD. Patients that hold a REGICOR CV risk score ≥7, and REASON risk core ≥7, during a routine primary care visit Exclusion Criteria: Symptomatic PAD Coronary disease Stroke Cardiac revascularization

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Intervention group PAD screening program

    Control group PAD screening program

    Arm Description

    Patients aged 50-74 years free of any symptomatic or history of CVD and a Framingham-REGICOR risk ≥7%, will be candidates for PAD screening program using REASON's function predicative capacity

    Patients aged 50-74 years free of any symptomatic or history of CVD will be candidates as a comparison group to calculate the cost-utility and reduction of CVD risk and events.

    Outcomes

    Primary Outcome Measures

    Hard coronary heart disease (CHD)
    Myocardial infarction, cardiac revascularization, or coronary death
    Major adverse cardiovascular event (MACE)
    A composite of hard CHD (myocardial infarction, cardiac revascularization, or coronary death) and stroke (fatal and nonfatal ischemic stroke)
    All-cause mortality
    Tabaco consumption (CVD risk factors improvement assessment)
    Smoker, ex-smoker or non-smoker
    Lipid profile (CVD risk factors improvement assessment)
    Total cholesterol (mg/dl), LDL (mg/dl), HDL (mg/dl), Triglycerides (mg/dl)
    Systolic and diastolic pressure (CVD risk factors improvement assessment)
    mm Hg
    Weight (CVD risk factors improvement assessment)
    kg
    Height (CVD risk factors improvement assessment)
    m
    BMI (CVD risk factors improvement assessment)
    (kg/m2) Will be calculated dividing the weight in kilograms by their height in metres squared
    Glycaemia (CVD risk factors improvement assessment)
    Fasting blood sugar (mg/dl)
    Glycated haemoglobin (CVD risk factors improvement assessment)
    (in DM patients) glycosylated hemoglobin in the blood (mg/dl) or percentage (%)
    Creatinine (CVD risk factors improvement assessment)
    mg/dL
    Proteinuria (CVD risk factors improvement assessment)
    mg/dL protein in urine
    Albumin-to-creatinine ratio (ACR) (CVD risk factors improvement assessment)
    ACR (mg/g) will be calculated by by dividing mg of proteinuria (albumine) by g of creatinine.
    Glomerular filtrate rate (CVD risk factors improvement assessment)
    Levels of creatinine in milliliters of cleansed blood per minute per body surface (mL/min/1.73m2).

    Secondary Outcome Measures

    Coronary heart disease
    A composite of angina and hard CHD
    Cerebrovascular disease
    A composite of stroke (fatal and nonfatal ischemic stroke) and transient ischemic attack
    Cardiovascular disease
    a composite of MACE, angina and transient ischemic attack
    Lipid lowering medication Adverse effects
    1) Short-term effects: Muscular and hepatic alterations, and 2) long-term effects: Diabetes and cancer

    Full Information

    First Posted
    May 10, 2023
    Last Updated
    July 31, 2023
    Sponsor
    Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
    Collaborators
    Hospital del Mar Research Institute (IMIM), Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta, Institut Català de la Salut, Biocruces Bizkaia Health Research Institute
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05884840
    Brief Title
    New Cardiovascular Risk Screening Strategy.
    Acronym
    HELENA
    Official Title
    Health Program for prEvention of cardiovascuLar disEases Based on a Risk screeNing Strategy With Ankle-brachial Index.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 2023 (Anticipated)
    Primary Completion Date
    June 2026 (Anticipated)
    Study Completion Date
    June 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
    Collaborators
    Hospital del Mar Research Institute (IMIM), Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta, Institut Català de la Salut, Biocruces Bizkaia Health Research Institute

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    Mortality due to cardiovascular disease (CVD) in Spain accounted for 29% of all deaths (32% in women and 26% in men) in 2017. Out of those, 67% were related to a coronary or a cerebrovascular disease . A key strategy in primary prevention of CVD is to use risk functions to individualize preventive interventions for each patient. The current CV risk-screening program in some regions of Spain, is based using an adapted Framingham scale, REGICOR's risk function, which is integrated in the primary care electronic health record. This risk function predicts the probability within 10 years of developing a coronary event. However, this function fails to identify patients that fall into low- or intermediate-risk level, and might develop a CV event in the up following 10 years. Ankle-brachial index (ABI) is a simple, non-invasive and economic technique, which allows detecting peripheral arterial disease (PAD), and gives independent risk function information compared to other coronary risk functions. Even tough, between 13-27% of middle age population have an ABI ≤ 9, around 50-89% of them do not exhibit any symptoms. However, they hold higher mortality risk and CV events. Current clinical guidelines for PAD screening, have a limited level of evidence, and only recommend using ABI on patients aged 50-70, who have diabetes or are smokers, and patients older than 70 years old. A new risk function, REASON, to assess CVD risk has been designed. This model has proven to improve predictive capacity of holding an ABI ≤ 0.9 on those patients aged 50-74 that are apparently free of CVD. Therefore, a strategy that combines the current CV risk estimation using REGICOR, and the prediction capacity of pathologic ABI with REASON, would allow detecting high-risk patients with a PAD screening program. It is possible that patients, who hold an ABI ≤ 0.9, even if being asymptomatic, will adopt physician's recommendations on healthy life habits and preventive treatment. The aims of this study are: To assess the effectiveness and cost-utility of adding a screening program with ABI to the current strategy of CV risk detection to reduce the incidence of CVD and mortality from all causes in the population aged 50 to 74. To assess the effectiveness of adding a screening program with ABI to the current strategy of CV risk detection to improve cardiovascular risk factors in the population aged 50 to 74.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cardiovascular Prevention, Screening, Peripheral Artery Disease, Arteriosclerosis, Asymptomatic

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    This study will be conducted as a clustered randomized pragmatic clinical trial (CRT) in primary care practice. During the period of two years (2023-2025), randomization of the eight Health Regions (274 primary care centres) in Catalonia will take place. The current strategy, in Catalonia, for cardiovascular risk screening is based on risk assessment using Framingham-REGICOR risk function. In the intervention group, a screening program with ABI will be added to all 50-74-year-old individuals with Framingham-REGICOR risk ≥7% and high probability of having ABI≤0.9. The probability of having ABI≤0.9 will be estimated using the REASON function and will be defined as a probability ≥7%. People that are classified as ABI≤0.9 high-risk, will undergo a PAD screening program using ABI test. If the result of the ABI is equal and lower than 0.9, indications of the Health Catalan Institute's CV and lipid guidelines will be recommended by physicians to the patients.
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    54000 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Intervention group PAD screening program
    Arm Type
    Experimental
    Arm Description
    Patients aged 50-74 years free of any symptomatic or history of CVD and a Framingham-REGICOR risk ≥7%, will be candidates for PAD screening program using REASON's function predicative capacity
    Arm Title
    Control group PAD screening program
    Arm Type
    No Intervention
    Arm Description
    Patients aged 50-74 years free of any symptomatic or history of CVD will be candidates as a comparison group to calculate the cost-utility and reduction of CVD risk and events.
    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    HELENA
    Intervention Description
    The current CV risk screening program in based using the REGICOR risk function, which is integrated in the primary care electronic health record. This risk function predicts the probability within 10 years of developing a coronary event. Those who are categorized as high risk, obtaining a 10% of probability, are candidates of receiving lipid lowering drugs and recommendations on healthy life habits. What this intervention suggests is that, besides the REGICOR estimation, the electronic health records will also incorporate a new CV risk function, REASON. The model predicts the risk of holding a pathologic ABI score, in people aged 50-74 years old who are apparently free of CV. Patients who obtain a score ≥ 7 will undergo a PAD screening program with ABI test. If the value of the test is ≤0.9, the REGICOR, physicians will recommend indications of the Health Catalan Institute's CV and lipid Guidelines to the patients.
    Primary Outcome Measure Information:
    Title
    Hard coronary heart disease (CHD)
    Description
    Myocardial infarction, cardiac revascularization, or coronary death
    Time Frame
    3 years
    Title
    Major adverse cardiovascular event (MACE)
    Description
    A composite of hard CHD (myocardial infarction, cardiac revascularization, or coronary death) and stroke (fatal and nonfatal ischemic stroke)
    Time Frame
    3 years
    Title
    All-cause mortality
    Time Frame
    3 years
    Title
    Tabaco consumption (CVD risk factors improvement assessment)
    Description
    Smoker, ex-smoker or non-smoker
    Time Frame
    3 years
    Title
    Lipid profile (CVD risk factors improvement assessment)
    Description
    Total cholesterol (mg/dl), LDL (mg/dl), HDL (mg/dl), Triglycerides (mg/dl)
    Time Frame
    3 years
    Title
    Systolic and diastolic pressure (CVD risk factors improvement assessment)
    Description
    mm Hg
    Time Frame
    3 years
    Title
    Weight (CVD risk factors improvement assessment)
    Description
    kg
    Time Frame
    3 years
    Title
    Height (CVD risk factors improvement assessment)
    Description
    m
    Time Frame
    3 years
    Title
    BMI (CVD risk factors improvement assessment)
    Description
    (kg/m2) Will be calculated dividing the weight in kilograms by their height in metres squared
    Time Frame
    3 years
    Title
    Glycaemia (CVD risk factors improvement assessment)
    Description
    Fasting blood sugar (mg/dl)
    Time Frame
    3 years
    Title
    Glycated haemoglobin (CVD risk factors improvement assessment)
    Description
    (in DM patients) glycosylated hemoglobin in the blood (mg/dl) or percentage (%)
    Time Frame
    3 years
    Title
    Creatinine (CVD risk factors improvement assessment)
    Description
    mg/dL
    Time Frame
    3 years
    Title
    Proteinuria (CVD risk factors improvement assessment)
    Description
    mg/dL protein in urine
    Time Frame
    3 years
    Title
    Albumin-to-creatinine ratio (ACR) (CVD risk factors improvement assessment)
    Description
    ACR (mg/g) will be calculated by by dividing mg of proteinuria (albumine) by g of creatinine.
    Time Frame
    3 years
    Title
    Glomerular filtrate rate (CVD risk factors improvement assessment)
    Description
    Levels of creatinine in milliliters of cleansed blood per minute per body surface (mL/min/1.73m2).
    Time Frame
    3 years
    Secondary Outcome Measure Information:
    Title
    Coronary heart disease
    Description
    A composite of angina and hard CHD
    Time Frame
    3 years
    Title
    Cerebrovascular disease
    Description
    A composite of stroke (fatal and nonfatal ischemic stroke) and transient ischemic attack
    Time Frame
    3 years
    Title
    Cardiovascular disease
    Description
    a composite of MACE, angina and transient ischemic attack
    Time Frame
    3 years
    Title
    Lipid lowering medication Adverse effects
    Description
    1) Short-term effects: Muscular and hepatic alterations, and 2) long-term effects: Diabetes and cancer
    Time Frame
    3 years

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    50 Years
    Maximum Age & Unit of Time
    74 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients aged 50 to 74, which are free or do not have previous history of CVD. Patients that hold a REGICOR CV risk score ≥7, and REASON risk core ≥7, during a routine primary care visit Exclusion Criteria: Symptomatic PAD Coronary disease Stroke Cardiac revascularization
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Rafel Ramos Blanes, MD, PhD
    Phone
    +34 972 48 79 68
    Email
    rramos.girona.ics@gencat.cat
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Rafel Ramos Blanes, MD, PhD
    Organizational Affiliation
    Unidad de Investigación en Atención Primaria de Girona, IDIAP Jordi Gol
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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