CARAMEL Observational Study

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age40-60
SponsorBiogipuzkoa Health Research Institute

About this trial

CARAMEL is a project funded by the European Commission under the Horizon Europe programme. Its aim is to develop a personalized prevention approach based on state-of-the-art artificial intelligence models for cardiovascular risk stratification in women aged 40-60 years. These models are trained using large amounts of multi-source data and complemented by digital self-assessment and self-management tools. The CARAMEL consortium brings together a diverse group of 25 organizations, including technology companies and research centers, clinical institutions, as well as experts in ethics, law, and communication.

The CARAMEL-OS study is an observational study aimed at prospectively completing the proposed personalized cardiovascular risk stratification model for women aged 40-60 years that will be developed during the earlier phases of the overall CARAMEL project (https://www.caramel-project.eu/).

The study has a purely observational design, and patient stratification will not entail any clinical intervention. The data collected will be used to complete the design of the personalized stratification model, as well as to develop and validate the performance of the predictive models in an independent prospective cohort, distinct from the retrospective cohort initially used. The performance of the models developed using retrospective data will be assessed in terms of accuracy, discrimination, calibration, and other relevant metrics. In addition, the study will enable the development of new predictive models with short-term prediction horizons, incorporating additional variables that are not available retrospectively.

The study population will be recruited in four European Union countries: Croatia, Spain (Andalusia and The Basque Country - Gipuzkoa), Greece and Lithuania; and in Colombia. A prospective cohort of 3,000 women aged 40-60 will be recruited, with each partner contributing 500 participants.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Women 40 to 60 years of age, at recruitment.

Ability to understand and complete the required informed consent for the study.

Women who are covered by the corresponding healthcare system operating at each clinical site.

Disqualifiers

Severe comorbidity with less than 24 months life expectancy.

Lack of basic digital skills to use or carry a smartphone and wearable devices.

Trial population

The study population will be recruited in four European Union countries: Croatia, Spain (Andalusia and The Basque Country - Gipuzkoa), Greece and Lithuania; and in Colombia. A prospective cohort of 3,000 women aged 40-60 will be recruited, with each partner contributing 500 participants. Eligible women may be invited to participate by their regular healthcare provider or may express their interest independently. To maximize representativeness, information about the study will be disseminated via multiple communication channels, including social media platforms (e.g., LinkedIn, Facebook, Bluesky, X). Women who express interest will be contacted by the CARAMEL research team, and detailed study documentation will be provided.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

3,000 Participants
are grouped into 1 trial group
Group A: 3,000 women aged 40-60 recruited in four European Union countries and Colombia.

Trial outcomes

Primary outcomes

1

Incidence of hypertension

Incidence of hypertension will be assessed by measuring blood pressure during the baseline and final study visits, as well as by reviewing the diagnosis of hypertension recorded in the electronic health records. Participants enrolled during a self-monitoring month will be asked to measure their blood pressure twice daily throughout 1 month.

Time frame
From enrollment to program completion, spanning 21-24 months depending on the enrollment date.
2

Incidence of dyslipidaemia

Incidence of dyslipidaemia will be assessed through blood tests measuring HDL cholesterol, LDL cholesterol, total cholesterol, and triglyceride levels at the baseline and final study visits, as well as by reviewing diagnoses of dyslipidaemia recorded in the electronic health records.

Time frame
From enrollment to program completion, lasting 21-24 months depending on the enrollment date.
3

Incidence of diabetes mellitus

Incidence of diabetes mellitus will be assessed through blood tests measuring glomerular filtration rate, albumin-to-creatinine ratio, glucose and glycated hemoglobin levels at the baseline and final study visits, as well as by reviewing diagnoses of diabetes mellitus recorded in the electronic health records.

Time frame
From enrollment to program completion, lasting 21-24 months depending on the enrollment date.
4

Incidence of cardiovascular disease

The incidence of cardiovascular disease will be assessed through the diagnosis of the following conditions: myocardial infarction, chronic coronary syndrome, peripheral arterial disease, and stroke. This information will be collected through a structured medical history interview and by reviewing the electronic health records. These data will be collected during the baseline visit and the final visit.

Time frame
From enrollment to program completion, spanning 21-24 months depending on the enrollment date.

Secondary outcomes

1

Mortality of cardiovascular events.

Mortality of cardiovascular events will be assessed through review of electronic health records, collecting information on new cardiovascular events and mortality occurring during the follow-up period and identified at the final assessment.

Time frame
From enrollment to program completion, spanning 21-24 months depending on the enrollment date.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Biogipuzkoa Health Research Institute

Lead sponsor

Fundación Centro de Tecnologías de Interacción Visual y Comunicaciones Vicomtech

Collaborator

Keralty SAS

Collaborator

Particle Summary

Collaborator

iBreve Limited

Collaborator

Magdalena Clinic

Collaborator

Andaluz Health Service

Collaborator

AE. Fundación Pública Andaluza para la gestión de la investigación en salud de Sevilla

Collaborator

Viesoji Istaiga Vilniaus Universiteto Ligonine Santaros Klinikos

Collaborator

Asociación Centro de Investigación Cooperativa en Biociencias

Collaborator

Ulma Medical Technologies S Coop

Collaborator

Smartnanosenose Innovation

Collaborator

ETHNIKO KAI KAPODISTRIAKO PANEPISTIMIO ATHINON

Collaborator