Nutrition, HealthyNCT07508709
Personalized Nutrition During Pregnancy
A study testing Ninemoons app in people with Nutrition, Healthy and Nutrition Poor, run by Jefferson Drapkin at 1 site in United States.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 to 62 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Nutrition, Healthy, Nutrition Poor, Pregnancy Related
- What is being tested?
- Ninemoons app
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 0 participants
- Where
- 1 siteUnited States
- Study dates
- 18 Dec 2022to 15 Mar 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 62 years
- Women only
- Healthy volunteers accepted
- Adult
Who may be able to join
- Pregnant women are less then 20 weeks gestation
Who cannot join
- High-risk patients with severe obesity (BMI >35), existing pre-conditions such as diabetes, hypertension, cardiac abnormalities, and need for special medical attention
Trial locations and contacts
1 site in 1 country.
United States1 site
Women's Primary Care Clinic
Brooklyn, New York, 11220
About this study
Official title: Examining the Effect of Hyper-personalized Nutrition Advice for OBGYN Patients on Health and Wellbeing Outcomes During and After Pregnancy
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.
Read the 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.
- Conditions
- Nutrition, Healthy, Nutrition Poor, Pregnancy Related
- Being tested
- Ninemoons app
- Medical subject headings
- Malnutrition
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Ninemoons appOther
Individuals in the intervention arm will receive DNA specific nutritional advice on the nine moons app during pregnancy
| Study group | Role | What they receive |
|---|---|---|
| Nutrition intervention | Experimental | Not described Receives: Other: Ninemoons app |
| standard nutrition | No intervention | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
Rate of cesarean section vs. normal vaginal delivery
c-section rate
Measured: 9 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Apr 2026
- Study start18 Dec 2022
- Primary completion15 Mar 2024
- Study completion15 Mar 2024
Why it stopped: Study stopped due to prinicpal investigator leaving instution
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Nutrition, HealthyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- Jefferson Drapkin
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Jefferson Drapkin, Maimonides Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07508709
- Sponsor's protocol ID
- 2022-03-15
- Status last verified
- Sep 2026
- First submitted
- 6 Dec 2022
- Last updated
- 17 Sep 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 17 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Examining the Effect of Hyper-personalized Nutrition Advice for OBGYN Patients on Health and Wellbeing Outcomes During and After Pregnancy
- ClinicalTrials.gov ID
- NCT07508709
- Acronym / sponsor ID
- 2022-03-15
- Conditions
- Nutrition, Healthy, Nutrition Poor, Pregnancy Related
- Study type
- Interventional
- Recruitment status
- WithdrawnReason stopped: Study stopped due to prinicpal investigator leaving instution
- Enrolment
- 0 participants (actual)
- Lead sponsor
- Jefferson DrapkinUniversity, hospital or other
- Study start
- 18 Dec 2022 (actual)
- Primary completion
- 15 Mar 2024 (actual)
- Study completion
- 15 Mar 2024 (actual)
- First posted
- 2 Apr 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Nutrition intervention | Experimental | Other: Ninemoons app |
| standard nutrition | No intervention | – |
Who may qualify
- Ages
- 18 to 62 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (1 listed)
- Pregnant women are less then 20 weeks gestation
Key exclusion criteria (1 listed)
- High-risk patients with severe obesity (BMI >35), existing pre-conditions such as diabetes, hypertension, cardiac abnormalities, and need for special medical attention
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Ninemoons appIndividuals in the intervention arm will receive DNA specific nutritional advice on the nine moons app during pregnancy | Other | Nutrition intervention |
Primary outcome
Rate of cesarean section vs. normal vaginal delivery
Time frame: 9 months
c-section rate
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Sep 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Ninemoons app in people with Nutrition, Healthy and Nutrition Poor, run by Jefferson Drapkin at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: withdrawn, as of the sponsor's last update on 17 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was withdrawn before enrolling participants, so there are no results.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Rate of cesarean section vs. normal vaginal delivery (time frame: 9 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Sep 2026; AzTrials last refreshed its copy on 29 Oct 2026.