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Active, Not Recruiting

NCT Number: NCT03300713

MOther-Child Interaction Assessment TRAINING for Pediatricians

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Conditions

Child Behavior Disorders Depression, Postpartum Depressive Disorder Female Urogenital Diseases and Pregnancy Complications Mental Disorders Mood Disorders Mother-Child Relations Neurodevelopmental Disorders Pregnancy Complications Puerperal Disorders Urogenital Diseases

Age range

23 day–37 day

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU

Lille, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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).

Treatment and study plan

MOCITRAINING program

Other

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

Other

usual follow-up

Primary outcomes

  1. Frequency of pathological Alarm Distress BaBy (ADBB) scores

    Time frame: in 12-month-aged children.

Secondary outcomes

  1. Frequency of pathological Alarm Distress BaBy (ADBB) scores

    Time frame: in 4, 9 and 24 month-aged children

  2. Frequency of digestive disorders

    Time frame: in 4, 9, 12 and 24 month-aged children

    presence/absence of infantile regurgitations and colics

  3. Number of daytime sleep hours

    Time frame: in 4, 9, 12 and 24 month-aged children

  4. Number of nighttime awakenings

    Time frame: in 4, 9, 12 and 24 month-aged children

  5. Scores on maternal self-evaluation scales (Likert scales)

    Time frame: 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)

  6. Frequency of dyads referred for psychiatric or perinatal psychiatric consultations

    Time frame: in 4, 9, 12 and 24 month-aged children

  7. Frequency of maternal psychotropic medication

    Time frame: in 4, 9, 12 and 24 month-aged children

Sponsors and collaborators

Lead sponsor

University Hospital, Lille

Other

Collaborators

  • Ministry of Health, France

Registry information

Acronym: MOCITRAINING

Important dates

Study start
2017
Primary completion
2026
Study completion
2026
First posted
Oct 3, 2017
Registry last updated
May 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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