Nutrition in High-Risk Pregnancy

2

Review clinical trials related to Nutrition in High-Risk Pregnancy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Accelerating Healthcare Engagement in Healthy Food Interventions - Food Rx in High Risk Pregnant Mothers With About Fresh and Community Health Choice

The purpose of the study is to assess if the Fresh Connect food prescription (Fresh Connect Food Rx) program that provides consistent access to healthy fresh produce through purchases at the grocery store plus nutrition education impacts gestational weight gain, other pregnancy and birth outcomes, and food and nutrition security in low-income, ethnically diverse, at-risk women residing in Houston, Texas. Enrollment of participants will begin in pregnancy at the time of the first prenatal visit (as long as the first visit occurs before the end of the first trimester); each participant will be followed until 60 days post-partum (up to 11 months follow-up per participant).

Participants needed: 620
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: The University of Texas Health Science Center, HoustonUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Less than or equal to 20 weeks medically confirmed viable pregnancy [+1]

Does not Speak English or Spanish

Status: Recruiting

Accelerating Healthcare Engagement in Healthy Food Interventions - Food Rx in High Risk Pregnant Mothers With About Fresh and Community Health Choice

The purpose of the study is to assess if the Fresh Connect food prescription (Fresh Connect Food Rx) program that provides consistent access to healthy fresh produce through purchases at the grocery store plus nutrition education impacts gestational weight gain, other pregnancy and birth outcomes, and food and nutrition security in low-income, ethnically diverse, at-risk women residing in Houston, Texas. Enrollment of participants will begin in pregnancy at the time of the first prenatal visit (as long as the first visit occurs before the end of the first trimester); each participant will be followed until 60 days post-partum (up to 11 months follow-up per participant).

Participants needed: 620
Trial details
Age: 18-44Biological sex: FemaleType: InterventionalSponsor: The University of Texas Health Science Center, HoustonUpdated: Jul 8, 2025Locations: 1
Eligibility criteria

high-risk pregnant mothers receiving care at Texas Children's Health Plan (TCHP)... [+2]

not a high-risk pregnant mother receiving care at Texas Children's Health Plan (...