MOther-Child Interaction Assessment TRAINING for Pediatricians

Not Applicable

Recruiting

• Conditions: Child Behavior Disorders; Depression, Postpartum; Mother-child Relations
• Interventions: Other: usual follow-up; Other: MOCITRAINING program

• Registration Number: NCT03300713
• Lead Sponsor: University Hospital, Lille

Brief Summary

The originality of the MOCITRAINING study lies in the integration of infant and maternal care during the pediatric consultation and the assessment of the impact of this type of care in the short and medium term on The MOCITRAINING program could contribute to improving the quality of parent-child interactions.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2017-09-28
• Study First Submitted QC: 2017-09-28
• Study First Posted: 2017-10-03
• Study Start: 2017-12-02
• Status Verified: 2022-09
• Last Update Submitted: 2022-09-30
• Last Update Posted: 2022-10-03
• Primary Completion: 2026-12
• Study Completion: 2026-12

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 3504

Inclusion Criteria

• Each child will be included WITH his biological mother at the first-month visit after birth.
• Age: 1 month + / - 15 days (child), accompanied by his biological mother
• Mother able to read French;
• Signed consent letter after complete information of parents about the MOCITRAINING study, its principle, advantages and disadvantages.

Exclusion Criteria

• Preterm babies.
• Children from a twin or multiple pregnancy.
• Children with somatic diagnosis explaining the presence of digestive, sleeping or interactional disorders.
• Refusal to participate after clear information about the study;
• Refusal to sign the consent letter;
• Refusal to be informed of a diagnostic hypothesis;
• Participants not covered by the Social Security system;
• Participants incapable of consenting or under legal protection (guardianship or curatorship).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
F- group (usual follow-up)	usual follow-up	grouping 8 pediatricians' clusters. They will not receive the initial training on early interactional disorders and PND screening
F+ group (Mocitraining program)	MOCITRAINING program	including 8 pediatricians' clusters. F+ pediatricians will attend a specific training focused on mother-child interactions, maternal psychiatric disorders, particularly PND screening and early interventions for non-psychiatric physician.

Primary Outcome Measures

Name	Time	Method
Frequency of pathological Alarm Distress BaBy (ADBB) scores	in 12-month-aged children.

Secondary Outcome Measures

Name	Time	Method
Frequency of dyads referred for psychiatric or perinatal psychiatric consultations	in 4, 9, 12 and 24 month-aged children
Frequency of digestive disorders	in 4, 9, 12 and 24 month-aged children	presence/absence of infantile regurgitations and colics
Number of daytime sleep hours	in 4, 9, 12 and 24 month-aged children
Number of nighttime awakenings	in 4, 9, 12 and 24 month-aged children
Scores on maternal self-evaluation scales (Likert scales)	at 12 and 24 months postpartum	Scores on maternal self-evaluation scales (Likert scales) about parent-child relations (Items concerning comfort and pleasure during interactions)
Frequency of maternal psychotropic medication	in 4, 9, 12 and 24 month-aged children
Frequency of pathological Alarm Distress BaBy (ADBB) scores	in 4, 9 and 24 month-aged children

Trial Locations

Locations (1)

CHU; 🇫🇷 Lille, France