Actively Recruiting
M-O-M-S on the Bayou: Implementation of an Intervention for Mental Health in Pregnancy
Led by Tulane University · Updated on 2025-09-24
240
Participants Needed
1
Research Sites
108 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Disasters have negative effects in the short term (physical trauma, adverse environmental exposures, and unstable housing) and the long term (relocation, changes in family functioning, and negative economic effects), which interact with social determinants to worsen health among the most vulnerable women, infants, and communities. Trauma and severe stress are directly linked to pregnancy complications, and raise blood pressure during pregnancy, alter stress hormones, and increase vulnerability to infection, all of which predispose to reduced fetal growth and preterm birth. Disasters also worsen mental health, and depression during pregnancy and postpartum, for instance, is associated with worse physical health during pregnancy, maternal impairment, poorer quality parenting, negative child behavior, and poorer infant cognitive development.The goal of this intervention is to improve mental health in pregnant women living in a disaster-affected region. The main questions this intervention aims to answer are: * Assess the implementation outcomes (acceptability, adaptation, adoption, feasibility, fidelity, and sustainability) of a pilot intervention in a disaster recovery environment. * Assess the effectiveness of the M-O-M-S pilot intervention in a disaster recovery environment. The study will recruit pregnant women in areas that have experienced a natural disaster. Women will be recruited in early pregnancy and attend a series of classes on the cognitive and relationship changes of pregnancy and motherhood, and mental preparation for labor, led by a "mentor," a mother who has experienced pregnancy, labor, and motherhood.
CONDITIONS
Official Title
M-O-M-S on the Bayou: Implementation of an Intervention for Mental Health in Pregnancy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant
- Below 20 weeks' gestation
- Enrolled in prenatal care
You will not qualify if you...
- Not pregnant
- Under age 18
- Does not speak English or Spanish
- Does not plan to carry to term
- Does not plan to remain in the study area through pregnancy
- Fetal defects likely to lead to death or extensive hospitalization postpartum
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Tulane University
New Orleans, Louisiana, United States, 70112
Actively Recruiting
Research Team
E
Emily Harville, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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