Actively Recruiting

Phase Not Applicable
Age: 23Days - 37Days
All Genders
NCT03300713

MOther-Child Interaction Assessment TRAINING for Pediatricians

Led by University Hospital, Lille · Updated on 2022-10-03

3504

Participants Needed

1

Research Sites

469 weeks

Total Duration

On this page

Sponsors

U

University Hospital, Lille

Lead Sponsor

M

Ministry of Health, France

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

MOther-Child Interaction Assessment TRAINING for Pediatricians

Who Can Participate

Age: 23Days - 37Days
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Child is accompanied by their biological mother at the first-month visit after birth
  • Child's age is 1 month plus or minus 15 days
  • Mother is able to read French
  • Parents have signed a consent letter after being fully informed about the study, including its principles, advantages, and disadvantages
Not Eligible

You will not qualify if you...

  • Baby was born prematurely
  • Child is from a twin or multiple pregnancy
  • Child has a medical condition causing 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
  • Participant is not covered by the Social Security system
  • Participant is unable to consent or is under legal protection such as guardianship or curatorship

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHU

Lille, France

Actively Recruiting

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Research Team

R

Renaud Jardri, MD,PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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