FEAST Perinatal Support Program Intervention

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity of Southern California

About this trial

Latino individuals face an elevated risk of adverse health outcomes during pregnancy, impacting both the birthing parent and the baby with potential long-term chronic health conditions. While promoting a healthy diet during pregnancy is a promising strategy, interventions targeting dietary behaviors have yielded mixed results and lack widespread dissemination in communities in need. Collaborating with community-based organizations could enhance cultural relevance, build trust with Latino families, and improve program reach and effectiveness. Food Education Access Support Together (FEAST) is a community-based program that promotes healthy eating, well-being, and health equity for diverse, under-resourced urban populations in Los Angeles. The newly developed FEAST Perinatal Support Program (PSP) aims to support individuals through pregnancy and postpartum by providing dietary psychoeducation, skill-building, and social support, with an additional component of grocery gift cards to address food access barriers. This study proposes a pilot trial to assess the feasibility and preliminary efficacy of the FEAST PSP in enhancing dietary outcomes, overall health, and socio-cognitive precursors, in pregnant individuals. The study will enroll 40 pregnant adults in a single-arm study who will receive the core PSP with a $15 gift card for healthful fresh food (PSP+giftcard). Pre- and post-intervention assessments will include questionnaires, dietary recalls, physical measurements, and interviews to evaluate program perceptions. Specific aims include evaluating program feasibility and acceptability (i.e., reach, retention, and participant perceptions) and determining preliminary efficacy on changing socio-cognitive and behavioral aspects of diet, self-reported health, and cardiometabolic risk factors. The project aligns with goals of improving health outcomes in Latino families in Southern California and supports FEAST's strategic objectives for improving health and wellness of individuals during pregnancy and throughout the lifespan. The findings will inform program refinement and future NIH grants for rigorous evaluation of the FEAST PSP.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Currently pregnant

Speak and read English

Eligible for Electronics Benefit Transfer (EBT) and/or Women, Infants, and Children (WIC) benefits

Disqualifiers

Inability to attend in-person sessions

Trial design

Design model

Single group

Treatments tested in this trial

  • FEAST Perinatal Support Program

    Behavioral

    The intervention will include the core perinatal support program (PSP) with $15 weekly grocery gift cards for healthful food (fruit, vegetables, whole grains), The PSP will be completed during weekly group sessions over 16 weeks. The core PSP includes the two primary behavior change techniques: group-based nutrition education based on current United States Department of Agriculture (USDA) national guidelines for pregnant individuals and guided group sharing and engagement.

Treatment groups

40 Participants
are divided into 1 treatment group
Group A: FEAST Perinatal Support ProgramExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Mini-EAT 9-item score

Aggregate score of 9 items on the Mini-EAT survey

Time frame
Survey at baseline and immediately post-assessment
2

Healthy Eating and Weight Self-Efficacy (HEWSE) score

The HEWSE is a self-report questionnaire that assesses healthy eating and healthy weight self-efficacy. The scores range from 1-5 with higher scores indicating better self-efficacy.

Time frame
Current self-efficacy at baseline and immediately post-assessment
3

Motivation for Dietary Self-Control Scale score

The Motivation for Dietary Self-Control Scale is a self-report questionnaire that assesses motivations for dietary change with three sub scales: Dietary Goal-Desire Incongruence, Motivation for Dietary Self-control, and Satisfaction with Dietary Behavior. The scores for each subscale range from 0-6 with higher scores indicating better motivation.

Time frame
Current motivation at baseline and immediately post-assessment

Secondary outcomes

1

Patient-Reported Outcomes Measurement Information System (PROMIS) 29 Profile v2.0 score

The PROMIS is a self-report questionnaire measuring overall physical and mental health. PROMIS scores range from 0-5 with higher scores indicating worse mental and physical health.

Time frame
Past 7-day symptoms at baseline and immediately post-assessment
2

Body Mass Index value

Body mass index is calculated using measured height and weight. Higher scores indicate greater obesity risk.

Time frame
Current at baseline and immediately post-assessment
3

Hemoglobin A1C (HbA1c) recording

HbA1c is calculated using finger prick blood test. Values typically range from 5 to 12 with lower scores indicating less diabetes risk.

Time frame
Current at baseline and immediately post-assessment

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Southern California

Lead sponsor

National Institute on Minority Health and Health Disparities (NIMHD)

Collaborator

Children's Hospital Los Angeles

Collaborator