First reporting submitted

Including: Updates on 11 work packages, 20 financial statements, a technical report with more than 70 pages and much more information.

A big thank you to all partners for timely submission!


SC meeting in Leiden 2019, July 1 – 3

RECAP’s 6th Steering Committe meeting took place in Leiden (NL) on 1-3 July 2019. We were very pleased that the coordinator Prof Vincent Jaddoe of the LifeCycle project took part in the meeting as a guest speaker.


Recent and upcoming events

  • 6th SC Meeting: 1-3 July 2019 in Leiden
  • 3rd GA Meeting: 22-24 January 2019 in Rome
  • 4th SC Meeting: 4-6 July 2018 in Helsinki
  • 2nd GA Meeting: 16-18 January 2018 in Frankfurt am Main
  • 2nd SC Meeting: 6-7 September 2017 in Leiden

Our vision

Improve health, development and quality of life of babies born preterm

Although very preterm or very low weight births constitute fewer than 2% of all births across Europe, they account for up to half of perinatal and infant deaths, children with impairments and disabilities and more than a third of the health and educational budgets for children.

In addition to the increased risk for physical impairments, babies born the earliest and the smallest are also at higher risks of psychological and social problems than infants born at term. The RECAP preterm Project aims to understand the causes of these difficulties faced by very preterm children and adults in order improve the health, development and quality of life of these individuals.

Why is this important?

A strong and unique network

Extensive cohort studies and the collation of large amounts of data

The key to finding the causes as well as the treatment and prevention options for preterm babies lies in extensive cohort studies and the optimal use of of large amounts of data on very children. The RECAP preterm Project aims at using these two elements to discover new pre- and postnatal risk factors.

In order to reach this goal, we will set up the RECAP preterm Cohort Platform, a unique and powerful network of experts from various disciplines as well as parent and patient organizations. The network includes the major longitudinal studies in Europe and around the world and will assemble massive amounts of data that will reflect broad geographic, cultural and health system diversity.

Learn more