Examining attachment in children born prematurely

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to assess the attachment representations of children born prematurely at ages 3 and 5, focusing on their neurocognitive and behavioral development. It explores how prematurity affects parent-child interactions and the establishment of secure attachments, considering factors such as maternal sensitivity and responsiveness. The study utilizes questionnaires and interviews to gather data from parents and caregivers, providing insights into the long-term effects of prematurity on attachment. The research is conducted at Angers and Nantes University Hospitals, involving children who were part of a regional monitoring network for vulnerable newborns.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Children born in the neonatal reanimation department of Angers and Nantes University Hospitals
* Extrem preterm infants (term of birth less than or equal to 28 weeks of amenorrhea)
* Children included in the regional monitoring network for vulnerable newborns (Réseau Grandir Ensemble en Pays de la Loire, RGE)
* Children with a follow-up consultation at age 3 scheduled as part of the classic RGE follow-up on the Angers and Nantes University Hospitals
* Informed consent dated and signed by the parents or the holder of the parental authority
* Affiliated to a Social Security scheme

Exclusion Criteria:

* Child with severe neurocognitive impairment or severe autism trait-type behavioral disorder in the 2-year RGE follow-up evaluation

Where it's running

• University Hospital of Angers
  Angers, France Recruiting
• University Hospital of Nantes
  Nantes, France Not yet recruiting

Study contacts

• Principal investigator: Elise Riquin, MD — University Hospital of Angers
• Study coordinator: Denise Jolivot, MD
• Email: DeJolivot@chu-angers.fr
• Phone: 33-2-41-35-58-08

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.