Guidelines for Infant Feeding for First-Time Parents

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This trial aims to provide first-time parents with enhanced information on complementary feeding through a paper brochure and a smartphone application. The intervention will compare the effects of this dual approach against usual care, which consists solely of the brochure. Parents will receive targeted messages and videos via the app from the time their child is 3 months old until they reach 36 months, focusing on responsive feeding practices. The primary goal is to assess the impact of this intervention on the BMI z-score of infants at 36 months and on parental feeding practices.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* first-time parents
* child age is between 1 and 54 days
* parents living in Dijon and its surroundings (\~ 70 km around Dijon)
* parents who master enough the french language to understand and answer self-reported questionnaires

Exclusion Criteria:

* no affiliation to a social security scheme
* parents of a child born before 31 weeks of amenorrhea
* parents of a child presenting since birth with pathologies likely to have a strong impact on his diet or his feeding habits (allergy to cow's milk proteins, feeding through a nasogastric tube or gastrostomy, congenital defect of the digestive tract, oral feeding disorders)
* parents of a child with a multiple pregnancy (≥ 3 children).
* in the event of a twin birth, the follow-up for this study only focuses on one of the children (according to a random draw)
* additional exclusion criteria for participation in filmed meals from the age of 11 months: children with food allergies or intolerances or suffering from celiac disease.

Where it's running

• Centre des Sciences du Goût et de l'Alimentation
  Dijon, France Recruiting

Study contacts

• Principal investigator: Camille Schwartz, PhD — Inrae Umr Csga
• Study coordinator: Camille Schwartz, PhD
• Email: camille.schwartz@inrae.fr
• Phone: 00 333 80 69 37 43

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.