Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
84 participants
INTERVENTIONAL
2022-05-16
2025-05-30
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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Dual interventions
Receive both interventions: MamaMeals and MamaMatters Interventions
Meals
12 weeks of medically tailored meals
Meals + Social Support
12 weeks of medically tailored meals and12 weeks of social media based support
Meals intervention only
MamaMeals
Meals
12 weeks of medically tailored meals
Control
Wait-list control (received MamaMeals between 16-20 weeks postpartum) (after primary data collection time point)
Control
Waitlist Control Group (no intervention for first 4 months and then receive MamaMeals between 16-20 weeks postpartum)
Interventions
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Meals
12 weeks of medically tailored meals
Meals + Social Support
12 weeks of medically tailored meals and12 weeks of social media based support
Control
Waitlist Control Group (no intervention for first 4 months and then receive MamaMeals between 16-20 weeks postpartum)
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* speak English,
* are between 20-40 completed weeks of pregnancy,
* are ages 18 years or older.
Exclusion Criteria
* 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.
18 Years
FEMALE
Yes
Sponsors
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Texas Tech University Health Sciences Center
OTHER
Responsible Party
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Locations
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Texas Tech University Health Sciences Center
Amarillo, Texas, United States
Countries
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Other Identifiers
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A22-4290
Identifier Type: -
Identifier Source: org_study_id
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