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Clinical Trials/NCT05484999
NCT05484999
Active, not recruiting
Not Applicable

The Maternal Well-Being Study: A Feasibility and Acceptability Trial of Postpartum Support Interventions

Texas Tech University Health Sciences Center1 site in 1 country84 target enrollmentMay 16, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postpartum Depression
Sponsor
Texas Tech University Health Sciences Center
Enrollment
84
Locations
1
Primary Endpoint
% of meals delivered to and consumed by subjects
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

This project aims to understand the local feasibility and acceptability of MamaMeals (a home-delivered nutritious, postpartum meal delivery program) and MamaMatters (a moderated social media-based peer support group) among peripartum women who are eligible for federal supplemental nutrition assistance programs such as The Special Supplemental Nutrition Program for Women, Infants and Children (WIC) or Supplemental Nutrition Assistance Program (SNAP). The investigators will conduct a prospective randomized controlled trial (RCT) of these two interventions among postpartum individuals. Analyses will be performed to determine the relative risk of postpartum depressive or anxiety symptoms (primary outcome) and overall well-being and maternal/infant health (secondary/exploratory outcomes) between groups. Findings from this pilot intervention study will inform a future, large RCT exploring the effectiveness of MamaMeals and/or MamaMatters on reducing postpartum mental health symptoms and cardiovascular morbidity among individuals with food insecurity during and after pregnancy.

Detailed Description

1. To assess the local feasibility and acceptability of MamaMeals (home-delivered, nutritious meals) during the 4th trimester for mothers with peripartum food insecurity. 2. To explore perceptions about receiving a medically-tailored meal delivery intervention during the 4th trimester (MamaMeals) among a diverse sample of peripartum individuals with food insecurity (FI). 3. To assess through a randomized trial the potential efficacy of the MamaMeals (nutritious, home-delivered meals) and MamaMatters (ehealth postpartum support) interventions on peripartum mood disorders (primary outcome), postpartum cardiometabolic risk\* (exploratory outcome), maternal wellbeing (exploratory outcome), and infant health (exploratory outcome) during the first 12 months following delivery. Hypothesis: Individuals who receive the MamaMeals + MamaMatters interventions will have lower Edinburgh Postpartum Depression Scale (EPDS) scores throughout the first 12 weeks postpartum compared to groups receiving only one intervention or the control group.

Registry
clinicaltrials.gov
Start Date
May 16, 2022
End Date
May 30, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • screen positive for food insecurity or qualify for any of the following governmental assistance programs Medicaid, WIC, SNAP, TANF,
  • speak English,
  • are between 20-40 completed weeks of pregnancy,
  • are ages 18 years or older.

Exclusion Criteria

  • type 1 diabetes
  • dietary contraindications (e.g., severe food allergy, or inflammatory bowel disease, celiac disease, chronic renal disease, bariatric surgery, short bowel syndrome)
  • an active eating disorder (self-reported)
  • hospitalization in the past 12 months for a mental health concern
  • a history of postpartum psychosis
  • Individuals with a history of being banned from any social media site will also be excluded.

Outcomes

Primary Outcomes

% of meals delivered to and consumed by subjects

Time Frame: 12 weeks

Feasibility of meal delivery social media support delivery

perception of the nutritious home delivered meal program

Time Frame: 12 weeks

subject engagement with interventions and perception of interventions

Secondary Outcomes

  • % of Edinburgh postnatal depression scale score >15 at 12 weeks postpartum(12 weeks)

Study Sites (1)

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