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MOther-Child Interaction Assessment TRAINING for Pediatricians

MOther-Child Interaction Assessment TRAINING for Pediatricians

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03300713
Acronym
MOCITRAINING
Enrollment
3504
Registered
2017-10-03
Start date
2017-12-02
Completion date
2026-12-01
Last updated
2026-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Child Behavior Disorders, Depression, Postpartum, Mother-child Relations

Keywords

Mass screening, Pediatrician training

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.

Interventions

OTHERMOCITRAINING program

The program is clinical and psychometric tools for screening for interactions and postpartum psychiatric disorders. The program will expose the existing care arrangements and the different possible orientations of the families according to the identified problem.

usual follow-up

Sponsors

University Hospital, Lille
Lead SponsorOTHER
Ministry of Health, France
CollaboratorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
23 Days to 37 Days
Healthy volunteers
No

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).

Design outcomes

Primary

MeasureTime frame
Frequency of pathological Alarm Distress BaBy (ADBB) scoresin 12-month-aged children.

Secondary

MeasureTime frameDescription
Frequency of pathological Alarm Distress BaBy (ADBB) scoresin 4, 9 and 24 month-aged children
Frequency of digestive disordersin 4, 9, 12 and 24 month-aged childrenpresence/absence of infantile regurgitations and colics
Number of daytime sleep hoursin 4, 9, 12 and 24 month-aged children
Number of nighttime awakeningsin 4, 9, 12 and 24 month-aged children
Scores on maternal self-evaluation scales (Likert scales)at 12 and 24 months postpartumScores on maternal self-evaluation scales (Likert scales) about parent-child relations (Items concerning comfort and pleasure during interactions)
Frequency of dyads referred for psychiatric or perinatal psychiatric consultationsin 4, 9, 12 and 24 month-aged children
Frequency of maternal psychotropic medicationin 4, 9, 12 and 24 month-aged children

Countries

France

Contacts

PRINCIPAL_INVESTIGATORRenaud Jardri, MD, PhD

University Hospital, Lille

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 23, 2026