M-O-M-S on the Bayou: Implementation of an Intervention for Mental Health in Pregnancy
Part of paid clinical trials in New Orleans, Louisiana.
- Sponsor
- Tulane University
- Study ID
- NCT05838404
- Status
- Recruiting
Conditions
- Anxiety
- Depression
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- M-O-M-S on the Bayou — BEHAVIORALPeer and mentor support and meetings across pregnancy
Study Details
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.
Key Dates
- Start date
- Nov 1, 2023
- Status verified
- Sep 2025
- Primary completion
- Nov 30, 2025
- Completion
- Nov 30, 2025
Study Design
- Enrollment
- 240 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- PREVENTION
Arms
- Experimental: MOMS on the Bayou Intervention GroupParticipants complete intervention protocol.
Primary Outcome Measure
Pregnancy-specific anxiety [ Time Frame: 12 weeks ]
Central Contacts
- Emily Harville, PhD504-988-7327
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Tulane University | New Orleans | Louisiana | 70112 | Emily Harville 504-988-7327 Andrea Meyer 504-988-8803 |
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