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Recruiting Observational

AttachMent Preterm in the Loire Infant Follow-up Team

NCT04304846 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2021-01-07
Last updated
2024-06-11

Condition(s) studied

Preterm Birth

Investigational drug(s) / intervention(s)

Questionnaires and interviews

Questionnaires and interviews: List of questionnaires: ASQ, PSI, PPQ, SDQ, GSA and AMMI score obtained from mother during two separated interviews for the mother and the child at 3 and 5 years old

Study summary

The purpose of this study is to describe the attachment representations of children born prematurely at age 3 and 5 with regard to their neurocognitive and behavioral development.

Eligibility

Sex
ALL
Min age
3 Years
Max age
6 Years
Healthy volunteers
No
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

Primary outcome measure(s)

  • Attachment Story Completion Task — Three and five years after preterm birth
    The evaluation of attachment representations will be realized at two stages of development, using attachment story stems to complete (Attachment Story Completion Task; Bretherton, Ridgeway \& Cassidy, 1990), which is the gold standard tool for measuring this variable between the ages of 3 and 7. Four scores measuring security, deactivation, hyperactivation and disorganization are obtained with the coding system described by Miljkovitch (Miljkovitch et al. 2003). Score on each scale vary from -1 to +1.

Trial sites (2)

FacilityCityRegionStatus
University Hospital of Angers Angers France Recruiting
University Hospital of Nantes Nantes France Not Yet Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04304846 on ClinicalTrials.gov ↗ ← All trials in France