Actively Recruiting
Cardiovascular Risk Assessment in Young Women After Index Pregnancy With and Without Placental Complications
Led by Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau · Updated on 2026-01-21
1260
Participants Needed
1
Research Sites
174 weeks
Total Duration
On this page
Sponsors
F
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Lead Sponsor
H
Hospital Sant Joan de Deu
Collaborating Sponsor
AI-Summary
What this Trial Is About
In this project, the investigators aim to study how all these factors determine the cardiovascular status of a total of 1,800 mothers, 3 to 6 years after delivery. In addition, the investigators want to assess whether lifestyle and living conditions after childbirth may improve or worsen this imprint, since women often prioritize their families over themselves, making it more difficult to maintain a healthy lifestyle that could reduce their cardiovascular risk. Furthermore, the investigators will evaluate how environmental exposures influence their health, as well as explore potential strategies for prediction and prevention. The goal is to develop an easy-to-use algorithm or test that allows women and their physicians to assess this risk, ideally in the form of a mobile app. Although predictive algorithms for cardiovascular health already exist, most have been developed using predominantly male or older populations, and none have taken into account pregnancy-related events or environmental exposure - both of which are key determinants of women's cardiovascular health.
CONDITIONS
Official Title
Cardiovascular Risk Assessment in Young Women After Index Pregnancy With and Without Placental Complications
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who participated in the BiSC, EuroPE, or AngioCor cohort studies
- Delivered within the previous 3 to 6 years
- Provided written consent to participate in this study
You will not qualify if you...
- Unwillingness to participate in this study
- Probability of loss to follow-up
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hospital de la Santa Creu i de Sant Pau
Barcelona, Spain, 08025
Actively Recruiting
Research Team
E
Elisa Llurba Olivé, PhD
CONTACT
P
Pablo García Manau, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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