Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

Support program for mental health in pregnant women affected by disasters

Official title: M-O-M-S on the Bayou: Implementation of an Intervention for Mental Health in Pregnancy

Run by Tulane University · NCT05838404 · Data updated 2026-11-12

This study is testing a support program for pregnant women affected by disasters to see if it can help reduce anxiety and depression during pregnancy.

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Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment240 (estimated)
SponsorTulane University
Academic / other
Locations1 site (New Orleans, Louisiana)
StatusRecruiting
StartedNovember 1, 2023
Main results expectedNovember 30, 2025
Study endsNovember 30, 2025
Registry record updatedSeptember 24, 2025
Trial IDNCT05838404 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are pregnant women under 20 weeks' gestation who are enrolled in prenatal care.

Probably not a fit

Patients who may not benefit from this study include those under 18, non-English or non-Spanish speakers, and those with fetal defects likely to lead to death or extensive hospitalization postpartum.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This intervention aims to improve mental health outcomes for pregnant women living in disaster-affected regions by implementing the M-O-M-S™ (Mentors Offering Maternal Support) program. The program focuses on addressing pregnancy-specific anxiety and depressive symptoms through peer support and education led by experienced mothers. Women in early pregnancy will participate in classes that cover cognitive and relationship changes during pregnancy, as well as mental preparation for labor. The study will recruit up to 400 participants, with a goal of 240 completing the intervention, and will compare outcomes between those receiving the intervention and a control group.

Why it matters

Potential benefit: If successful, this intervention could significantly enhance the mental health and overall well-being of pregnant women in disaster-affected areas.

How similar studies have gone: Other studies have shown success with similar peer support interventions for mental health during pregnancy, indicating a promising approach.

Who can join: the full rules

Show full inclusion / exclusion 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

Where it's running

  • Tulane University
    New Orleans, Louisiana, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.