Assessment of the Mental State of Parents of Premature Children and Impact on Neurodevelopment of the Child (PoPPY)

March 2, 2026 updated by: University Hospital, Angers

Assessment of the Mental State of Parents of Premature Children and Impact on Neurodevelopment of the Child (Parents Psychic Preterm)

The objective of the study is to assess the psychic profile of parents of children born prematurely

Study Overview

Status

Active, not recruiting

Intervention / Treatment

Detailed Description

Prematurity affects aroound 1 in 10 children worlwide. Many studies have shown the role of prematurity in the development of depression, anxiety, post-traumatic stress disorder, mother-to-child attachment disorders, but few studies have sought to assess the evolution of this profile over time as well as to assess all of the parents' psychic dimensions.

The investigators currently have little knowledge of risk factors (psychological or psychiatric history, follow-up undertaken, treatments implemented, etc.) that may favor the occurrence of postpartum mental disorders (anxiety, depression, post-traumatic stress disorder ).

The investigators will thus seek to identify them. Prematurity can have a negative impact on the parents' psychic experience in the postpartum period. However, few studies have examined the evolution over time of the parental psychic profile and its possible repercussions on the child in terms of attachment and becoming neurodevelopmental. Finally, the majority of studies dealing with these subjects concern only mothers.Tthe investigators will endeavor here to also take into account the fathers.

Study Type

Observational

Enrollment (Estimated)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Angers, France
        • CHU Angers
      • Toulouse, France
        • CHU Toulouse

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Children born prematurely hospitalizes in the neonatalogy department of the Angers University Hospital and included in the cohort 'Réseau Grandir Ensemble en Pays de la Loire'.

Description

Inclusion Criteria:

Parents whose child meets the following criteria:

  • Singleton child
  • Child aged up to 40 weeks of amenorrhea of age corrected at the time of inclusion
  • Premature child as defined below:

    • Born at a term less than or equal to 34 weeks of amenorrhea And or
    • weighing 1500g or less at birth
  • Hospitalized in the neonatology department of the Angers University Hospital
  • Child included in Réseau Grandir Ensemble (RGE) in Pays de la Loire
  • Informed consent form signed by both parents for their participation and the collection of data from the RGE for the child

Non-inclusion Criteria:

  • Parents not fluent in the French language, implying not being able to complete the various questionnaires
  • Parents including the child :

    • Is from a twin pregnancy or more
    • Has polymalformative syndrome or chromosomal abnormalities

Exclusion Criteria:

- Death of the child or one of the parents during follow-up

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
PoPPY Group
Mother, Father and child born prematurely
Questionnaires (EPDS, HADS, PPQ, MIBS, etc.) will have to be completed by the parents at different stages of their child's development (38 weeks of amenorrhea, 3 months and 24 months).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assessing the psychic profile of parents of children born prematurely
Time Frame: At 38 weeks of amenorrhea (+/- 2 weeks)

The psychic profile of the parents will be evaluated from the score obtained in the following autoquestionnaire :

- parental depression (Edinburgh Postnatal Depression Scale (EPDS)), a score greater than or equal to 10 is in favour of parental depression

At 38 weeks of amenorrhea (+/- 2 weeks)
Assessing the psychic profile of parents of children born prematurely
Time Frame: At 38 weeks of amenorrhea (+/- 2 weeks)

The psychic profile of the parents will be evaluated from the score obtained in the following autoquestionnaire :

- parental anxiety (Hospital Anxiety and Depression Scale (HADS)), a score greater than or equal to 11 of the sub-scale anxiety is in favor of a parental anxiety

At 38 weeks of amenorrhea (+/- 2 weeks)
Assessing the psychic profile of parents of children born prematurely
Time Frame: At 38 weeks of amenorrhea (+/- 2 weeks)

The psychic profile of the parents will be evaluated from the score obtained in the following autoquestionnaire :

- posttraumatic stress parental ( Perinatal Posttraumatic Stress disorder Questionnaire (PPQ)), a score greater than or equal to 6 is in favour of posttraumatic parental stress

At 38 weeks of amenorrhea (+/- 2 weeks)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Study the evolution of parents' psychic profile over time
Time Frame: At 3 months corrected age and at 24 months corrected age
Use of the same tools and criteria as at 38 weeks of amenorrhea (parental depression : score EPDS ≥ 10)
At 3 months corrected age and at 24 months corrected age
Study the evolution of parents' psychic profile over time
Time Frame: At 3 months corrected age and at 24 months corrected age
Use of the same tools and criteria as at 38 weeks of amenorrhea (parental anxiety HADS ≥11)
At 3 months corrected age and at 24 months corrected age
Study the evolution of parents' psychic profile over time
Time Frame: At 3 months corrected age and at 24 months corrected age
Use of the same tools and criteria as at 38 WA (posttraumatic stress parental : PPQ ≥ 6)
At 3 months corrected age and at 24 months corrected age
Investigate the presence of peritraumatic dissociation experiments
Time Frame: At 38 weeks of amenorrhea (+/- 2 weeks)
A score greater than 15 from the PDEQ (Peritraumatic Dissociative Experiences Questionnaire) is considered a score in favour of a significant traumatic dissociation. Minimum scale value : 10, full scale value : 50. Abnormal if greater than or equal to 15.
At 38 weeks of amenorrhea (+/- 2 weeks)
Assess the mother's attachment to her child
Time Frame: At 38 weeks of amenorrhea and 3 months corrected age of the child
A score equal to or greater than 2 from the MIBS questionnaire (Mother To Infant Bonding Scale) highlights mother-child disorders. This questionnaire is given only to the mother. Minimum scale value : 0, full scale value : 24. Abnormal if greater than or equal to 2.
At 38 weeks of amenorrhea and 3 months corrected age of the child
Assess the parental stress
Time Frame: At 24 months corrected age
A PSI (Parenting Stress Index) high score (percentile rank greater than or equal to 85) is considered a score in favour af a parental stress. Minimum scale value : 0, full scale value : 180. Abnormal if greater than or equal to 85.
At 24 months corrected age
study perinatal or prenatal psychological and psychiatric factors associated with depression, anxiety and post traumatic stress
Time Frame: at 38 weeks of amenorrhea (+/- 2 weeks), and 3 months corrected age and at 24 months corrected age
these factors are studied by assessing whether or not there is a psychological and / or psychiatric history, medical-psychological follow-up, treatments taken.
at 38 weeks of amenorrhea (+/- 2 weeks), and 3 months corrected age and at 24 months corrected age
Study the impact of the parental psychic profile on the neurological development of the child
Time Frame: At 24 months corrected age

A ASQ (Ages Stages Questionnaire) score less than 185 is considered not optimal.

The other data collected during the evaluation of the 24 months of age corrected as part of the Réseau Grandir Ensemble (RGE) will be used for the evaluation of neurological development. These data make it possible to classify children's development into optimal or non-optimal according to a rating system which has been defined by the network's scientific council.The impact of the parental psychic profile (at 38 WA +/- 2 weeks, at 3 months and at 24 months of their child's corrected age) on neurological development will be evaluated by Odds Ratios (ORs): ORs measuring the association between the parental psychic profile and the non-optimal ASQ score, ORs measuring the association between the parental psychic profile and the non-optimal development category according to the RGE rating.

At 24 months corrected age

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 26, 2020

Primary Completion (Actual)

April 26, 2024

Study Completion (Estimated)

August 26, 2026

Study Registration Dates

First Submitted

September 1, 2020

First Submitted That Met QC Criteria

March 29, 2021

First Posted (Actual)

April 1, 2021

Study Record Updates

Last Update Posted (Actual)

March 4, 2026

Last Update Submitted That Met QC Criteria

March 2, 2026

Last Verified

March 1, 2026

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Parent-Child Relations

Clinical Trials on questionnaires

Subscribe