NCT03506971

Brief 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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
128

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2018

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 16, 2018

Completed
2 months until next milestone

First Posted

Study publicly available on registry

April 24, 2018

Completed
5 months until next milestone

Study Start

First participant enrolled

September 10, 2018

Completed
3.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 14, 2022

Completed
1.9 years until next milestone

Study Completion

Last participant's last visit for all outcomes

January 31, 2024

Completed
Last Updated

September 5, 2023

Status Verified

September 1, 2023

Enrollment Period

3.5 years

First QC Date

February 16, 2018

Last Update Submit

September 1, 2023

Conditions

Keywords

Young child's developmentHome visitsEarly interactionsattachmentparenthood

Outcome Measures

Primary Outcomes (14)

  • 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

  • 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

  • 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

  • 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

  • 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

  • Q-SORT attachment

    Q-SORT for evaluate the attachment

    24 months

  • 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

  • BDI : Beck Depression Inventory (13 items)

    This is a multiple-choice self-report inventory for measuring the severity of depression

    24 Months

  • 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

  • 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

  • HAQ : Helping Alliance Questionnaire

    Evaluate the therapeutic alliance

    3 months

  • HAQ

    Helping Alliance Questionnaire, to evaluate the therapeutic alliance

    24 months

  • Bobigny's early childhood interactions assessment

    It's an assessment of early childhood interactions baby-mother

    3 months

  • Bobigny's early childhood interactions assessment

    It's an assessment of early childhood interactions baby-mother

    24 months

Secondary Outcomes (1)

  • FAS : Family Affluence Scale

    3 and 24 Months

Study Arms (2)

Participants

EXPERIMENTAL

As part of this research, families will benefit from * "pediatric nurse's interventions" : home visits by a pediatric nurse who will center around three times: a time of observation of the development and progress of the baby, a time for play with the baby and a time to listening the parents. * "psychologist's evaluation" and "joint home visits" : home visits by the coordinating psychologist to evaluate three areas: child development, parenthood and parent-child interaction.

Other: Pediatric Nurse's interventionsOther: Joint home visits

Control

OTHER

"psychologist's evaluation" : home visits by the coordinating psychologist to evaluate three areas: child development, parenthood and parent-child interaction.

Other: Psychologist's evaluation

Interventions

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.

Control

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

Participants

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

Participants

Eligibility Criteria

Age1 Minute - 15 Days
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • Parents living in the Lunevillois area
  • Mother to be 8 months pregnant
  • Baby who's born from january to december 2018

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre Psychothérapique de Nancy

Laxou, 54200, France

Location

Related Publications (1)

  • Buchheit S, Kabuth B, Colombo MC, Ligier F. Child Development and Early Interaction: PERL Research Protocol, a Preventive Home Visiting Program, Randomized Controlled Trial in France. Front Psychiatry. 2021 Jun 30;12:641468. doi: 10.3389/fpsyt.2021.641468. eCollection 2021.

Study Officials

  • Sophie BUCHHEIT

    Centre Psychothérapique de Nancy

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 16, 2018

First Posted

April 24, 2018

Study Start

September 10, 2018

Primary Completion

March 14, 2022

Study Completion

January 31, 2024

Last Updated

September 5, 2023

Record last verified: 2023-09

Data Sharing

IPD Sharing
Will not share

Locations