Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06428578 · ClinicalTrials.gov registry record · NA
Enhancing Food as Medicine Interventions for Food Insecure Postpartum Women in Central Texas
A NA study of Food Insecurity in Post Partum Women, sponsored by The University of Texas Health Science Center, Houston.
- Recruiting
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 2
- Study locations
NCT06428578: Recruiting NA study of Food Insecurity in Post Partum Women, sponsored by The University of Texas Health Science Center, Houston.
NCT06428578 is a NA study of Food Insecurity in Post Partum Women that is actively recruiting participants, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 100 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06428578, a NA study of Food Insecurity in Post Partum Women, is actively recruiting participants, sponsored by The University of Texas Health Science Center, Houston.
- RECRUITING
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 2
- Study locations
Study Summary
The purpose of this study is to compare the short-term and long term impacts of Food is the Best Medicine (FBM)-Virtual on diet quality, food security status, breastfeeding rates, mental health status, rates of home cooking, and rationing coping strategies relative to FBM-In Person among food insecure, postpartum women and to compare implementation outcomes across the FBM-Virtual and FBM-In Person using process data collected from the participants, Community Health Worker (CHW)s, and partner organizations.
Conditions Studied
Interventions
- OTHER FBM-In person
- OTHER FBM-Virtual
- OTHER home delivered food boxes
Study Locations (2)
Texas
- Ascension Seton Medical Center - Austin
- The University of Texas Health Science Center at Houston - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2024-01-01 |
| Est. Completion | 2025-06-30 |
| Phase | NA |
What NCT06428578 shows while recruiting
NCT06428578 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).
The record links to 1 condition, with Food Insecurity in Post Partum Women appearing as the primary indexed condition, and to 3 interventions - of which FBM-In person is the first listed.
NCT06428578 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT06428578 about?
NCT06428578 is a clinical study titled "Enhancing Food as Medicine Interventions for Food Insecure Postpartum Women in Central Texas". The purpose of this study is to compare the short-term and long term impacts of Food is the Best Medicine (FBM)-Virtual on diet quality, food security status, breastfeeding rates, mental health status, rates of home cooking, and rationing coping strategies relative to FBM-In Person among food insecu...
What is the current status of trial NCT06428578?
This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2024-01-01. Estimated completion is 2025-06-30.
What conditions does trial NCT06428578 study?
This clinical trial studies the following conditions: Food Insecurity in Post Partum Women.
What interventions are being tested in trial NCT06428578?
The interventions under investigation include: FBM-In person (OTHER), FBM-Virtual (OTHER), home delivered food boxes (OTHER).
Who is sponsoring clinical trial NCT06428578?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06428578 being conducted?
This trial has 2 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Food Insecurity in Post Partum Women
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06428578's enrollment target sits among peer trials
100 840th of 2000 higher than 1,081 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT01048281 · 100 participants
Clinical & Pathological Studies of Upper Gastrointestinal Carcinoma
- NCT01161199 · 100 participants
The Use of Leukapheresis to Support HIV Pathogenesis Studies
- NCT01327690 · 100 participants · Early Phase 1
Mental Health in Veterans and Families After Group Therapies
- NCT01730781 · 100 participants
Imaging Cannabinoid Receptors Using Positron Emission Tomography (PET) Scanning
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI