Examining attachment in children born prematurely
Attachment Representations of Children Born Prematurely in the Loire Infant Follow-up Team Cohort
This study looks at how being born prematurely affects the way young children connect with their parents and develop emotionally as they grow up.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 90 (estimated) |
| Ages | 3 Years to 6 Years |
| Sex | All |
| Sponsor | University Hospital, Angers Government |
| Locations | 2 sites (Angers and 1 other locations) |
| Trial ID | NCT04304846 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates include children born extremely preterm (≤28 weeks) who are part of the regional monitoring network and are scheduled for follow-up consultations at ages 3 and 5.
Not a fit: Patients with severe neurocognitive impairments or significant autism traits may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of attachment issues in prematurely born children, leading to improved support strategies for families.
How similar studies have performed: While studies on attachment in preterm infants exist, this specific approach focusing on the interplay between prematurity and attachment representations is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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 this trial is running
Angers and 1 other locations
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.