- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04827225
Assessment of the Mental State of Parents of Premature Children and Impact on Neurodevelopment of the Child (PoPPY)
Assessment of the Mental State of Parents of Premature Children and Impact on Neurodevelopment of the Child (Parents Psychic Preterm)
Study Overview
Status
Conditions
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
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
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Angers, France
- CHU Angers
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Toulouse, France
- CHU Toulouse
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
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
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Use of the same tools and criteria as at 38 weeks of amenorrhea (parental depression : score EPDS ≥ 10)
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At 3 months corrected age and at 24 months corrected age
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Study the evolution of parents' psychic profile over time
Time Frame: At 3 months corrected age and at 24 months corrected age
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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.
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At 38 weeks of amenorrhea (+/- 2 weeks)
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Assess the mother's attachment to her child
Time Frame: At 38 weeks of amenorrhea and 3 months corrected age of the child
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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
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Assess the parental stress
Time Frame: At 24 months corrected age
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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.
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At 24 months corrected age
|
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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.
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at 38 weeks of amenorrhea (+/- 2 weeks), and 3 months corrected age and at 24 months corrected age
|
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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
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Obstetric Labor, Premature
- Obstetric Labor Complications
- Pregnancy Complications
- Premature Birth
- Health Care Quality, Access, and Evaluation
- Investigative Techniques
- Epidemiologic Methods
- Data Collection
- Health Care Evaluation Mechanisms
- Quality of Health Care
- Public Health
- Environment and Public Health
- Surveys and Questionnaires
Other Study ID Numbers
- 49RC20_0132
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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