Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04845230
Other study ID # 202011018
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 9, 2021
Est. completion date September 15, 2026

Study information

Verified date November 2022
Source Washington University School of Medicine
Contact Stephen Roll, PhD
Phone 314-935-3710
Email stephen.roll@wustl.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is an evaluation of the Fresh Rx: Nourishing Healthy Starts program administered by Operation Food Search, a St. Louis-based nonprofit organization. The program provides food and nutrition supports to food insecure pregnant women in conjunction with integrative care services in order to improve health and birth outcomes for both the mother and the child. The purpose of this study is to test the efficacy of this approach through a field experiment, and to assess the extent to which these services can provide cost savings to the healthcare system.


Description:

This study is an evaluation of the Fresh Rx: Nourishing Healthy Starts program administered by Operation Food Search, a St. Louis-based nonprofit organization. The goal of the program is to provide food and nutrition supports to food insecure pregnant women in order to improve health and birth outcomes for both the mother and the child. Specifically, this program provides: - Facilitated access to food support programs like the Supplemental Nutrition Assistance Program (SNAP); Women, Infants, and Children (WIC); and food pantries - Direct food delivery to pregnant women, nutrition education, and access to a registered dietitian - Access to a social worker who will provide integrative care services Participants in this program will be recruited through a Medicaid Managed Care Organization (MCO). During their initial intake meeting with an MCO case manager, potential participants will be screened for food insecurity through the use of a two-item food insecurity screener. If a potential participant screens positive for food insecurity, she will be referred to Operation Food Search to begin the Nourishing Healthy Starts recruitment process. Consenting participants will be randomly assigned to one of three conditions (described in detail below), each of which provides the standard of care women would receive in the absence of the program plus additional program features. Control Group. The control group in this study will still receive some services above and beyond the usual standard of care offered to pregnant women on Medicaid. In addition to the case management services offered through their managed care provider, Operation Food Search will offer this group access to the "hunger hotline," a service provided by Operation Food Search to help them find food assistance around St. Louis; assistance in enrolling in public nutrition assistance programs like SNAP and WIC; and guidance on food pantry access in St. Louis. Treatment 1: Food Supplementation and Education Group. This treatment group will receive all the services offered to the control group, as well as the following services: 1. Weekly food deliveries of fresh food meal kits with step-by-step recipes from the time of program enrollment through 60 days post-partum; 2. Access to necessary cooking tools for their kitchen (e.g., spatulas, cutting boards , etc.), should they need them. 3. Access to online cooking resources to help guide them on culinary skills and recipe preparation. 4. Nutrition education and counseling provided by a registered dietitian. Treatment 2: Food Supplementation, Education, and Integrative Case Management. This treatment group will receive all the services offered to Treatment Group 1, as well as the services of a licensed social worker who will provide trauma-informed integrative care services to participants. These services will focus on an array of potential needs that may emerge in participants' lives, such as assistance in finding stable housing, assistance navigating social services, connections with other community organizations, and other needs. This evaluation will combine longitudinal survey data from participants with health claims data provided by the MCOs. Study participants will consent to have their data collected and linked for research purposes. The research team will not have access to any personally identifiable information on program participants, and the team will analyze a deidentified dataset. Each intervention approach will examine a different method of providing women with access to affordable, nutritious food throughout their pregnancy and through the early post-partum period. After it is determined how best to support food insecure women and their families, the evidence from this study may be used to make a case for treating healthy food supports as part of a new standard of care for food insecure pregnant women. The results will provide information to public health agencies, public insurance systems, Medicaid MCOs, and other insurance companies in order to help them understand the potential benefits of these food supports.


Recruitment information / eligibility

Status Recruiting
Enrollment 750
Est. completion date September 15, 2026
Est. primary completion date September 15, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 14 Years to 55 Years
Eligibility Inclusion Criteria: - Female - Pregnant - Less than 24 weeks gestation - Screening positive to a USDA two-item food insecurity screener (described below) - Receiving care through a Missouri Medicaid managed care organization - English speaking - Age 14-55 - Missouri resident residing in the following zip codes: 63031, 63033, 63042, 63074, 63114, 63121, 63130, 63132, 63133, 63135, 63136, 63137, 63138, 63140 Exclusion Criteria: - Male - Non-pregnant - Pregnant, but more than 24 weeks gestation - Does not screen positive to a USDA two-item food insecurity screener (described below) - Does not receive care through the Home State Health managed care organization - Non-English speaking - Aged less than 14 or more than 55 - Does not reside in the following zip codes: 63031, 63033, 63042, 63074, 63114, 63121, 63130, 63132, 63133, 63135, 63136, 63137, 63138, 63140

Study Design


Intervention

Behavioral:
FreshRx Nourishing Healthy Starts
This is a field experiment study that incorporates referrals to public programs, food supplementation and nutrition education, or integrative care services provided by a Licensed Masters Social Worker.

Locations

Country Name City State
United States Operation Food Search Inc. Saint Louis Missouri

Sponsors (2)

Lead Sponsor Collaborator
Washington University School of Medicine Operation Food Search Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Change in cooking skills Incidence of using basic and advanced kitchen tasks. Participants will be asked how often they perform an array of given tasks (Never, Rarely, Monthly, Weekly, Daily) such as boiling water, following a recipe, using a chef's knife, and so on, through a matrix question listing these tasks. Baseline, around 3 months post-baseline, 60 days post-partum, one year post-partum
Primary Change in food insecurity Repeated measures of food insecurity using United States Department of Agriculture (USDA) food insecurity screener Baseline, around 3 months post-baseline, 60 days post-partum, one year post-partum
Primary Gestational Age at Birth Estimated gestational age (in days) of the child on the delivery date Collected at time of birth
Primary Birthweight Weight (in grams) of infant at birth Collected at time of birth
Secondary Change in food spending A continuous measure asking about weekly expenditures on groceries and eating and restaurants, and other food options Baseline, around 3 months post-baseline, 60 days post-partum, one year post-partum
Secondary Change in self reported physical and mental health Measures captured using an abbreviated 5-item Patient Reported Outcomes Measurement Information System (PROMIS) screener Baseline, around 3 months post-baseline, 60 days post-partum, one year post-partum
Secondary Number of Prenatal Appointments Number of prenatal health appointments received during pregnancy Collected quarterly from enrollment through birth
Secondary Maternal Immunizations Received Pregnancy-related immunizations received (e.g., Tdap, influenza) during pregnancy Collected quarterly from enrollment through birth
Secondary Change in Maternal Platelet Count Change in lab results on platelet count from first prenatal visit to final prenatal visit Collected quarterly from enrollment through birth
Secondary Change in Maternal White Blood Cell Count Change in lab results on while blood cell count from first prenatal visit to final prenatal visit Collected quarterly from enrollment through birth
Secondary Change in Maternal Hematocrit Count Change in lab results on maternal hematocrit count from first prenatal visit to final prenatal visit Collected quarterly from enrollment through birth
Secondary Change in Maternal Hemoglobin Count Change in lab results on maternal hemoglobin count from first prenatal visit to final prenatal visit Collected quarterly from enrollment through birth
Secondary Change in Maternal Red Blood Cell Count Change in lab results on maternal red blood cell count from first prenatal visit to final prenatal visit Collected quarterly from enrollment through birth
Secondary Maternal Anemia Diagnosis Incidence of maternal anemia diagnosis at any point during pregnancy Collected quarterly from enrollment through birth
Secondary Fetal Complications Diagnosis Incidence of any common fetal complication diagnosis (e.g., ectopic pregnancy) at any point during pregnancy Collected quarterly from enrollment through birth
Secondary Hypertensive Disorder Diagnosis Incidence of any hypertensive disorder diagnosis at any point during pregnancy Collected quarterly from enrollment through birth
Secondary Spontaneous Preterm Labor Incidence of spontaneous preterm labor at any point during pregnancy Collected quarterly from enrollment through birth
Secondary Preeclampsia Diagnosis Incidence of preeclampsia diagnosis at any point during pregnancy Collected quarterly from enrollment through birth
Secondary Difficulty paying bills A single item measure capturing the incidence of bill payment difficulty in a typical month Baseline, around 3 months post-baseline, 60 days post-partum, one year post-partum
Secondary Post-partum depression Collected through the Edinburgh Post-partum Depression Scale. This scale is score 0 to 30, with higher values indicator higher risk for post-partum depression Baseline, around 3 months post-baseline, 60 days post-partum, one year post-partum
Secondary Intrauterine Fetal Demise (IUFD) Incidence of IUFD over course of pregnancy Collected quarterly from enrollment through birth
Secondary Spontaneous Abortion Incidence of spontaneous abortion over course of pregnancy Collected quarterly from enrollment through birth
Secondary Postpartum Complications Incidence of common postpartum physical health complications (e.g., hypertension, sepsis) Birth through 60 days post-partum
Secondary Adverse Post-Partum Mental Health Diagnoses Incidence of common postpartum adverse mental health diagnoses (e.g., anxiety, psychosis) Birth through 60 days post-partum
Secondary Maternal Mortality Incidence of maternal mortality Birth through 60 days post-partum
Secondary Infant mortality Incidence of infant mortality Birth through 60 days post-partum
Secondary Change in food quality A repeated assessment of the mix of foods consumed through the use of a 24-hour-recall-based food frequency questionnaire Baseline, around 3 months post-baseline, 60 days post-partum, one year post-partum
Secondary Emergency liquidity A single item indicator capturing how participants would cover a $400 emergency expense Baseline, around 3 months post-baseline, 60 days post-partum, one year post-partum
Secondary Public program participation A matrix question capturing the incidence of participation in common public welfare programs: Supplemental Nutrition Assistance (SNAP); Temporary Assistance for Needy Families (TANF); Public Housing/Housing Choice Vouchers; Women, Infants, and Children (WIC); Utility assistance; Child care assistance Baseline, around 3 months post-baseline, 60 days post-partum, one year post-partum
Secondary Maternal Hospital Admissions Measure of hospital admissions derived from health care claims data Collected quarterly from enrollment through one year post-partum
Secondary Maternal Emergency Room Visits Measure of emergency room visits derived from health care claims data Collected quarterly from enrollment through one year post-partum
Secondary Maternal Wellness Visits Measure of wellness visits derived from health care claims data Collected quarterly from enrollment through one year post-partum
Secondary Pediatric Visits Number of pediatric visits in the post-partum period Birth through one year post-partum
Secondary Infant Adverse Health Diagnoses Incidence of common infant adverse health diagnoses (e.g., colic, jaundice) Birth through one year post-partum
Secondary Days in Neonatal Intensive Care Unit (NICU) Length of NICU stay for infant following birth Collected from birth through 60 days post-partum
Secondary Admission to Special Care Nursery Incidence of admission to special care nursery Collected from birth through 60 days post-partum
Secondary Birth Defects Incidence of common birth defects (e.g., congenital heart defects, cleft palate) Collected from birth through 60 days post-partum
Secondary Child Weight Child weight (grams) post-birth Collected from birth through one year post-partum
Secondary Child Height Child height (centimeters) post-birth Collected from birth through one year post-partum
Secondary Child Hospital Admissions Number of Hospital Admissions for Child Following Birth Collected from birth through one year post-partum
Secondary Neonatal death Incidence of neonatal death Collected from birth through one year post-partum
Secondary Child Emergency Department Admissions Number of emergency department admissions following birth Collected from birth through one year post-partum
See also
  Status Clinical Trial Phase
Active, not recruiting NCT05048550 - Babies in Glasses; a Feasibility Study. N/A
Active, not recruiting NCT03655639 - Local Version of the Multi-center PREVENT Study Evaluating Cardio-respiratory Instability in Premature Infants
Enrolling by invitation NCT05542108 - Adding Motion to Contact: A New Model for Low-cost Family Centered Very-early Onset Intervention in Very Preterm-born Infants N/A
Completed NCT03680157 - Comparing Rater Reliability of Familiar Practitioners to Blinded Coders
Completed NCT03337659 - A Cluster Randomized Controlled Trial of FICare at 18 Months N/A
Completed NCT03649932 - Enteral L Citrulline Supplementation in Preterm Infants - Safety, Efficacy and Dosing Phase 1
Completed NCT03251729 - Cerclage On LOw Risk Singletons: Cervical Cerclage for Prevention of Spontaneous Preterm Birth in Low Risk Singleton Pregnancies With Short Cervix Phase 4
Not yet recruiting NCT05039918 - Neonatal Experience of Social Touch N/A
Not yet recruiting NCT03418012 - Prevention of sPTB With Early Cervical Pessary Treatment in Women at High Risk for PTB N/A
Not yet recruiting NCT03418311 - Cervical Pessary Treatment for Prevention of s PTB in Twin Pregnancies on Children`s Long-Term Outcome N/A
Not yet recruiting NCT02880696 - Perception of Temporal Regularity in Tactile Stimulation: a Diffuse Correlation Spectroscopy Study in Preterm Neonates N/A
Completed NCT02952950 - Is it Possible to Prolong the Duration of Breastfeeding in Premature Infants? a Prospectivt Study N/A
Completed NCT02913495 - Vaginal Versus Intramuscular Progesterone for the Prevention of Recurrent Preterm Birth Phase 4
Completed NCT02879799 - Family Integrated Care (FICare) in Level II NICUs N/A
Completed NCT02743572 - Iron-fortified Parenteral Nutrition in the Prevention and Treatment of Anemia in Premature Infants N/A
Completed NCT02661360 - Effects of Swaddling on Infants During Feeding N/A
Completed NCT01352234 - Comparison of Doses of Acetylsalicylic Acid in Women With Previous History of Preeclampsia Phase 4
Completed NCT01163188 - Social Adjustment and Quality of Life After Very Preterm Birth N/A
Terminated NCT00675753 - Three Interacting Single Nucleotide Polymorphisms (SNPs) and the Risk of Preterm Birth in Black Families N/A
Completed NCT00271115 - Kangaroo Holding and Maternal Stress N/A