Support program for mental health in pregnant women affected by disasters
M-O-M-S on the Bayou: Implementation of an Intervention for Mental Health in Pregnancy
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.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 240 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Tulane University Academic / other |
| Locations | 1 site (New Orleans, Louisiana) |
| Trial ID | NCT05838404 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are pregnant women under 20 weeks' gestation who are enrolled in prenatal care.
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.
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 performed: Other studies have shown success with similar peer support interventions for mental health during pregnancy, indicating a promising approach.
Eligibility criteria
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 this trial is running
New Orleans, Louisiana
- Tulane University — New Orleans, Louisiana, United States (Recruiting)
Study contacts
- Study coordinator: Emily Harville, PhD
- Email: eharvill@tulane.edu
- Phone: 504-988-7327
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.