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feediNg gUidelines infanT RandomIzEd coNtrolled Trial

The purpose of this randomized controlled trial is to conduct an intervention aimed at providing first-time parents with information on the conduct of complementary feeding through a paper brochure and a smartphone application, to test the effect of this intervention (compared to usual care, i.e. receiving the paper br

Condition(s)Healthy Volunteers
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryThe purpose of this randomized controlled trial is to conduct an intervention aimed at providing first-time parents with information on the conduct of complementary feeding through a paper brochure and a smartphone application, to test the effect of this intervention (compared to usual care, i.e. receiving the paper brochure only), on infant corpulence at 36 and 48 months of age, and parental feeding practices and infant eating behavior up to 36 months of age.
Who can participateInclusion 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 c
Ages18 Years
SexAll
Accepts healthy volunteersYes
Lead sponsorInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement
LocationsDijon, France
Start date2022-03-24
NCT IDNCT05285761
Official listinghttps://clinicaltrials.gov/study/NCT05285761

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