M-O-M-S on the Bayou: Implementation of an Intervention for Mental Health in Pregnancy
Tulane University · NCT05838404
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 240
- US sites recruiting
- 1
- Study start
- November 1, 2023
- Record last updated
- September 24, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study 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.
Being studied: M-O-M-S on the Bayou
Conditions: Anxiety; Depression
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Pregnant
- Below 20 weeks' gestation
- Enrolled in prenatal care
Exclusion Criteria
- 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
Recruiting US locations
Tulane University
New Orleans, LA 70112
Site contact: Emily Harville · 504-988-7327
Study contacts (from the official record)
- Emily Harville, PhD · 504-988-7327 · eharvill@tulane.edu
Similar studies in Louisiana
All mental health studies in Louisiana →- RecruitingHealthy volunteers
Observational Study of Decentralized Urine Optical Interaction Patterns Associated With Environmental Microplastic and Nanoplastic Exposure
Ecotera Health LLC
- Location
- New Orleans, LA + 50 other US sites
- Eligibility basics
- Ages 18+
- RecruitingPhase 3
A Study to Evaluate the Maintenance Effect of Osavampator as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)
Neurocrine Biosciences
- Location
- Marrero, LA + 19 other US sites
- Eligibility basics
- Ages 18+
- RecruitingPhase 2/Phase 3
ACP-204 in Adults With Alzheimer's Disease Psychosis
ACADIA Pharmaceuticals Inc.
- Location
- Shreveport, LA + 34 other US sites
- Eligibility basics
- Ages 55–95
- RecruitingPhase 3
A Study of a Deuterated Psilocin Analog (CYB003) in Humans With Major Depressive Disorder
Cybin IRL Limited
- Location
- New Orleans, LA + 27 other US sites
- Eligibility basics
- Ages 18–85