Overview
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.
Eligibility
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