SCORE2-Diabetes: 10-year cardiovascular risk estimation in type 2 diabetes in Europe.
SCORE2-Diabetes Working Group and the ESC Cardiovascular Risk Collaboration
https://pubmed.ncbi.nlm.nih.gov/37247330/Actively Recruiting
Led by Biogipuzkoa Health Research Institute · Updated on 2026-07-10
3000
Participants Needed
6
Research Sites
26 weeks
Total Duration
Researchers are conducting the CARAMEL-OS observational study to develop and validate personalized artificial intelligence models for assessing cardiovascular risk in women aged 40 to 60 years during their menopausal transition. This project involves a collaboration of 25 organizations across Europe and Colombia, aiming to improve cardiovascular disease prevention by integrating multi-source data, including socioeconomic, clinical, biochemical, imaging, and novel non-invasive variables related to female-specific risk factors and menopause. The study will recruit a prospective cohort of 3,000 women from six clinical sites in four European countries and Colombia, with 500 participants contributed per site. Participants will be observed without any clinical intervention, using digital self-assessment and self-management tools, including a mobile app designed to support women during menopause. Data collected will help refine cardiovascular risk stratification models and develop new predictive tools with short-term horizons. Participants will be involved in assessments spanning 21 to 24 months depending on enrollment, during which incidence of hypertension, dyslipidaemia, diabetes mellitus, and cardiovascular disease will be recorded. Mortality related to cardiovascular events will also be tracked. The study focuses on gathering comprehensive data through questionnaires, imaging, biochemical tests, and digital monitoring to support personalized prevention strategies and advance precision medicine in womens cardiovascular health.
CONDITIONS
CARAMEL Observational Study
P
Primary Care - OSIs Research Unit
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Biogipuzkoa Health Research Institute
Lead Sponsor
Fundación Centro de Tecnologías de Interacción Visual y Comunicaciones Vicomtech
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Duration - 21 to 24 months
Participants provide data through questionnaires, imaging, biochemical tests, and use of digital tools including a mobile app to track cardiovascular risk factors during menopause.
Regular assessments throughout the period
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Lead Sponsor
Fundación Centro de Tecnologías de Interacción Visual y Comunicaciones Vicomtech
Collaborating Sponsor