Efficacy of Family-based Dietary Counseling During Pregnancy on Gestational Weight Gain in Pregnant Women in a Randomized Controlled Trial
Recruiting now · Not applicable
Conditions studied: Pregnancy, Dietetics
In brief
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.
Key facts
- Study ID
- NCT06646965
- Run by
- University Hospital, Toulouse
- People needed
- 1374
- Starts
- 2025-01-13
- Expected to finish
- 2028-06-15
- Last updated by the study team
- 2025-07-02
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- 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
Where it is running
- Hospital of Auch — Auch, France (enrolling)
- Clinique Rive Gauche — Toulouse, France (enrolling)
- University Hospital of Toulouse — Toulouse, France (enrolling)
Full record on ClinicalTrials.gov
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