The study aims to evaluate the efficacy of a family-based dietary monitoring during pregnancy on gestational weight gain in pregnant women. The study will be conducted as a randomized controlled trial, women will be randomly allocated into two groups: a group receiving family-based dietary monitoring, and a control group receiving individual dietary monitoring per standard recommendation.
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Eligibility Criteria
Inclusion Criteria:
Adult (+18 years old) Pregnant woman who can be accompanied by a member of the household, adult sharing at least 1 meal per day with her. Affiliated to the social security. French speaking person (read/written and spoken). Single pregnancy between 8 SA and 16 SA. Starting BMI be…
Inclusion Criteria:
Adult (+18 years old) Pregnant woman who can be accompanied by a member of the household, adult sharing at least 1 meal per day with her. Affiliated to the social security. French speaking person (read/written and spoken). Single pregnancy between 8 SA and 16 SA. Starting BMI between 18.5 and 35
Exclusion Criteria:
* Person under legal protection or guardianship
* Women suffering from a disease requiring a dietary follow-up:
* Type 1 or type 2 diabetes.
* Gestational diabetes diagnosed on the basis of fasting blood sugar.
* History of bariatric surgery.
* Eating disorders.
* Metabolic pathologies leading to special diets (phenylketonuria).
* Digestive pathologies (with an indication) with special diets
* Women who have lost more than 10% of their weight at the beginning of pregnancy
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