Personalized Nutrition During Pregnancy

Examining the Effect of Hyper-personalized Nutrition Advice for OBGYN Patients on Health and Wellbeing Outcomes During and After Pregnancy

Status

Withdrawn

Phases

Unknown

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT07508709

Enrollment

Registered

2026-04-02

Start date

2022-12-18

Completion date

2024-03-15

Last updated

2026-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nutrition, Healthy, Nutrition Poor, Pregnancy Related

Brief summary

Dietary quality and total energy intake during pregnancy significantly influences the mother's health during pregnancy and that of the fetus as well as decade long influences on the health outcomes of the child. However, a one size fits all approach to nutritional guidance is far from ideal given the unique biological, lifestyle, demographic, and health condition differences of expecting mothers. This research proposal will examine the effect of precision nutrition on the health and wellbeing outcomes of mothers during pregnancy, at the time of delivery, and post-delivery. Personal nutritional guidance is based on personal biological, behavioral, and health data.

Detailed description

Participants will be recruited out of the Maimonides Women's Health Clinic. Each arm will recruit 75 participants. The intervention arm will receive a DNA swab which will be tested and then the patient will receive DNA specific nutrition advice on their smartphone via nine moons app. The other arm will receive no intervention and will only receive standard nutritional advice. Both arms will be followed up every 4 weeks to test vitals and height and weight. Delivery outcomes will be compared at the end of pregnancy.

Interventions

OTHERNinemoons app

Individuals in the intervention arm will receive DNA specific nutritional advice on the nine moons app during pregnancy

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

PREVENTION

Masking

NONE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 62 Years

Healthy volunteers

Yes

Inclusion criteria

* Pregnant women are less then 20 weeks gestation

Exclusion criteria

* High-risk patients with severe obesity (BMI \>35), existing pre-conditions such as diabetes, hypertension, cardiac abnormalities, and need for special medical attention

Design outcomes

Primary

Measure	Time frame	Description
Rate of cesarean section vs. normal vaginal delivery	9 months	c-section rate

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026