A web-based and mobile randomised controlled trial providing complementary feeding guidelines to first-time parents in France to promote responsive parental feeding practices, healthy children's eating behaviour and optimal body mass index: the NutrienT trial study protocol.


Journal

BMC public health
ISSN: 1471-2458
Titre abrégé: BMC Public Health
Pays: England
ID NLM: 100968562

Informations de publication

Date de publication:
27 Sep 2024
Historique:
received: 28 07 2023
accepted: 12 09 2024
medline: 28 9 2024
pubmed: 28 9 2024
entrez: 28 9 2024
Statut: epublish

Résumé

Childhood obesity is a crucial public health issue. Early childhood is a critical time to foster the establishment of healthy eating behaviours and growth, which are partly shaped by parental feeding practices. To inform French parents of the recently updated national complementary feeding guidelines for 0-3 years (in terms of nutrition and responsive feeding as a mean to encourage infant appetite control skills and promote healthy growth), an official printed brochure was developed and nationally disseminated in 2021 by the French public health agency, Santé publique France. This randomised controlled trial aims to investigate whether the provision of guidelines through digital (smartphone application) and printed (brochure) tools (vs. the printed brochure alone, usual service) results in healthier parental feeding practices, infant eating behaviours and weight status. This double-blinded monocentric 2-arm trial is currently conducted among first-time parents living in the area of Dijon (France) and recruited in a maternity ward. From child age 3 to 36 months (mo), an app provides a range of 106 age-adapted messages, including dietary recommendations, educational advice, recipes, and tips (intervention group only). Additionally, parents of both groups are provided with 48 messages related to child general development and the printed brochure at child age 2.7 mo. The primary outcome is the body mass index (BMI) z-score at child age 36 mo. Secondary outcome measures include a combination of online parents' reports and behavioural assessments (experimental meals) of parental feeding practices and infant eating behaviours from inclusion to 36 months of age. Analyses of covariance on these outcomes will assess the effect of the intervention, adjusted for relevant confounders. Complementary mediation and moderation analyses will be conducted. Sample size was determined to be n = 118 in each arm of the trial, plus 20% to compensate for potential attrition. This is the first public eHealth randomised control trial in France to assess the effect of a web-based and mobile intervention targeted to first-time parents to improve child feeding practices and child growth. This trial was registered at clinicaltrials.gov as NCT05285761 (March 18, 2022).

Sections du résumé

BACKGROUND BACKGROUND
Childhood obesity is a crucial public health issue. Early childhood is a critical time to foster the establishment of healthy eating behaviours and growth, which are partly shaped by parental feeding practices. To inform French parents of the recently updated national complementary feeding guidelines for 0-3 years (in terms of nutrition and responsive feeding as a mean to encourage infant appetite control skills and promote healthy growth), an official printed brochure was developed and nationally disseminated in 2021 by the French public health agency, Santé publique France. This randomised controlled trial aims to investigate whether the provision of guidelines through digital (smartphone application) and printed (brochure) tools (vs. the printed brochure alone, usual service) results in healthier parental feeding practices, infant eating behaviours and weight status.
METHODS METHODS
This double-blinded monocentric 2-arm trial is currently conducted among first-time parents living in the area of Dijon (France) and recruited in a maternity ward. From child age 3 to 36 months (mo), an app provides a range of 106 age-adapted messages, including dietary recommendations, educational advice, recipes, and tips (intervention group only). Additionally, parents of both groups are provided with 48 messages related to child general development and the printed brochure at child age 2.7 mo. The primary outcome is the body mass index (BMI) z-score at child age 36 mo. Secondary outcome measures include a combination of online parents' reports and behavioural assessments (experimental meals) of parental feeding practices and infant eating behaviours from inclusion to 36 months of age. Analyses of covariance on these outcomes will assess the effect of the intervention, adjusted for relevant confounders. Complementary mediation and moderation analyses will be conducted. Sample size was determined to be n = 118 in each arm of the trial, plus 20% to compensate for potential attrition.
DISCUSSION CONCLUSIONS
This is the first public eHealth randomised control trial in France to assess the effect of a web-based and mobile intervention targeted to first-time parents to improve child feeding practices and child growth.
TRIAL REGISTRATION BACKGROUND
This trial was registered at clinicaltrials.gov as NCT05285761 (March 18, 2022).

Identifiants

pubmed: 39334106
doi: 10.1186/s12889-024-20057-z
pii: 10.1186/s12889-024-20057-z
doi:

Banques de données

ClinicalTrials.gov
['NCT05285761']

Types de publication

Journal Article Randomized Controlled Trial Clinical Trial Protocol

Langues

eng

Sous-ensembles de citation

IM

Pagination

2649

Subventions

Organisme : Conseil régional de Bourgogne-Franche-Comté
ID : RECO-ALIM-BB
Organisme : Conseil régional de Bourgogne-Franche-Comté
ID : RECO-ALIM-BB
Organisme : Conseil régional de Bourgogne-Franche-Comté
ID : RECO-ALIM-BB
Organisme : EU ITN-EDULIA
ID : Marie Skłodowska-Curie grant agreement No 764985
Organisme : EU ITN-EDULIA
ID : Marie Skłodowska-Curie grant agreement No 764985
Organisme : EU ITN-EDULIA
ID : Marie Skłodowska-Curie grant agreement No 764985

Informations de copyright

© 2024. The Author(s).

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Auteurs

Camille Riera-Navarro (C)

Centre Des Sciences du Goût Et de L'Alimentation, CNRS, INRAE, Institut Agro, Université de Bourgogne, F-21000, Dijon, France.

Camille Schwartz (C)

Centre Des Sciences du Goût Et de L'Alimentation, CNRS, INRAE, Institut Agro, Université de Bourgogne, F-21000, Dijon, France.

Pauline Ducrot (P)

Santé Publique France, French National Public Health Agency, F-94415, Saint-Maurice, France.

Laurence Noirot (L)

Santé Publique France, French National Public Health Agency, F-94415, Saint-Maurice, France.

Corinne Delamaire (C)

Santé Publique France, French National Public Health Agency, F-94415, Saint-Maurice, France.

Edith Sales-Wuillemin (E)

Psy-DREPI (Psychologie: Dynamiques Relationnelles Et Processus Identitaires), Université de Bourgogne, EA 7458, F-21000, Dijon, France.

Denis S Semama (DS)

Department of Neonatal Pediatrics, CHRU Dijon, Dijon University Hospital, Dijon, France.

Sandrine Lioret (S)

Université Paris Cité and Université Sorbonne Paris Nord, Inserm, INRAE, Centre for Research in Epidemiology and StatisticS (CRESS, F-75004, Paris, France.

Sophie Nicklaus (S)

Centre Des Sciences du Goût Et de L'Alimentation, CNRS, INRAE, Institut Agro, Université de Bourgogne, F-21000, Dijon, France. sophie.nicklaus@inrae.fr.

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