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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03506971
Other study ID # RIPH 2017-01
Secondary ID IDRCB 2017-A0089
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date September 10, 2018
Est. completion date January 31, 2024

Study information

Verified date September 2023
Source Centre Psychothérapique de Nancy
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The PERL project is a research in prevention in perinatality. The objective of this research is to offer preventive and regular care at familie's home in the Lunévillois area, while integrating it into the existing practices of the maternal and child protection, in the framework of a partnership between the PMI (Protection Maternal Infantile) and the child psychiatry. An innovative prevention device to support the interactions and development of the child will be proposed to about sixty families, randomly recruited into the general population. If the family agrees to participate, their will benefit from regular home visits by a pediatric nurse, accompanied on certain times by a psychologist, for a period of 4 years from the birth of the child. This home-visits accompaniment, centered on listening and observation, focuses on three areas: baby's development, parenthood and parent-child's interactions. A longitudinal and comparative evaluation will be carried out with a "control" group recruited according to the same conditions and at the same time as the "participants" group. A parallel research on the processes and mechanism will be carried out in partnership with the School of Public Health in order to define and validate the intervention theory (what are the mobilized levers produced and how, what are the mechanisms linking the intervention to its results), to describe the implementation and the processes involved, and to analyze the effects of context, especially social, on processes and results.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 128
Est. completion date January 31, 2024
Est. primary completion date March 14, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 1 Minute to 15 Days
Eligibility Inclusion Criteria: - Parents living in the Lunevillois area - Mother to be 8 months pregnant - Baby who's born from january to december 2018 Exclusion Criteria: - No exclusion criteria

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Psychologist's evaluation
The research coordinator psychologist will evaluate: the development of the baby, the early interactions between the baby and his mother, attachment, maternal psychiatric symptoms, the experience of parenting and maternal sensitivity.
Pediatric Nurse's interventions
Pediatrics nurses perform preventive home visits that are based on : joint observation with the parents of the baby, play with the baby and his parents, interview with the parents on their parenthood Rhythm of home visits: 1 every month from birth to 1 year 1 every 2 months from 1 year to 2 years 1 every 3 months from 2 years to 4 years
Joint home visits
Coordinating psychologist and the referent pediatric nurse will perform home visits. During this time, the psychologist evaluate : the development of the baby, the early interactions between the baby and his mother, attachment, maternal psychiatric symptoms, the experience of parenting and maternal sensitivity. Rhythm of joint home visits: 1 at 4 months 1 at 24 months

Locations

Country Name City State
France Centre Psychothérapique de Nancy Laxou

Sponsors (4)

Lead Sponsor Collaborator
Centre Psychothérapique de Nancy Agence Regionale de Sante d'Ile de France, Conseil Départemental, Protection Maternelle Infantile :PMI, France, Family Allowance Fund, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Brunet-Lézine-revised test : assessment of change between 3 and 24 months and between two groups of the study. Assessment of children psychomotor development. This test can be used at any time from the age of 0 to 30 months 3 and 24 months
Primary ADBB (Alarm Distress BaBy) : assessment of change between 3 and 24 months and between two groups of the study. Filmed evaluation of relational withdrawal of young children. This evaluation can be used at any time from the age of 2 to 24 months 3 and 24 months
Primary EPDS : Edinburgh Postnatal Depression Scale The Edinburgh Postnatal Depression Scale (EPDS) is a set of 10 screening questions that can indicate whether a parent has symptoms that are common in women with depression and anxiety during pregnancy and in the year following the birth of a child.
To complete this set of questions, the parent should select the number next to the response that comes closest to how they have felt in the past seven days.
The total score is calculated by adding the numbers selected for each of the 10 items. If the parent's score is 10 points or above, they should speak to a health professional about those symptoms.
3 months
Primary ERP (Entretien sur les représentations Parentales, no traduction for acronym): assessment of change between 3 and 24 months and between two groups of the study. Interview on Parent's Representations 3 and 24 months
Primary ERTL 4 : Epreuve de repérage des Troubles du Langage = French questionnaire. No traduction for acronym Test of Spotting of language delays at 4 years, carried out in a systematic way by the teams of maternal and child protection 4 YEARS
Primary Q-SORT attachment Q-SORT for evaluate the attachment 24 months
Primary Mini-MBQS (Maternal Behavior Q-Sort ) : assessment of change between 3 and 24 months and between two groups of the study. 25 items to obtain an assessment of global maternal sensitivity 3 and 24 Months
Primary BDI : Beck Depression Inventory (13 items) This is a multiple-choice self-report inventory for measuring the severity of depression 24 Months
Primary SCL-90R (Symptom Checklist-90-R) : assessment of change between 3 and 24 months and between two groups of the study. Symptom check-list, self-assessment questionnaire for psychiatric symptoms 3 and 24 Months
Primary BITSEA : Brief Infant Toddler Social and Emotional Assessment Early screening of social and emotional difficulties or developmental delays for children. This assessment can be used at any time from the age of 12 to 36 months. 24 months
Primary HAQ : Helping Alliance Questionnaire Evaluate the therapeutic alliance 3 months
Primary HAQ Helping Alliance Questionnaire, to evaluate the therapeutic alliance 24 months
Primary Bobigny's early childhood interactions assessment It's an assessment of early childhood interactions baby-mother 3 months
Primary Bobigny's early childhood interactions assessment It's an assessment of early childhood interactions baby-mother 24 months
Secondary FAS : Family Affluence Scale Small questionnaire to describe family's affluence. 4 questions asked : How many computers do you have at home ? (none, 1, 2, more than 2) / Do you have a car at home? (no, 1, 2 or more) / Do you have your own bedroom at home? (yes, no) / For the last 12 months, how many times have you travelled with your family for holidays? (never, once, twice, more than twice) Assessment of change will be done between 3 and 24 months and between two groups of the study 3 and 24 Months
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