M-O-M-S on the Bayou: Implementation of an Intervention for Mental Health in Pregnancy
NCT ID: NCT05838404
Last Updated: 2025-09-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
240 participants
INTERVENTIONAL
2023-11-01
2025-11-30
Brief Summary
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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.
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Detailed Description
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Up to 400 subjects will be recruited, with a goal of 240 completing the study. Each group will consist of 15-20 recruits, assuming a degree of attrition that will lead to group sizes of 10-12. The outcome measures will be compared between the intervention and control data and linear regression (with adjustment for partial clustering) used to adjust for differences in participant characteristics. Given an estimated effect size and variance (both pre-post and intervention-control) from previous trials, 240 participants gives good power for reasonable effect sizes for both the pre-post analysis and intervention-control analyses incorporating a design (cluster) effect.
Recruitment will take place at ob/gyn practices, WIC clinics, health units, and at community sites. Clinicians will be informed of the intervention and asked to encourage their patients to participate. They will also refer potential participants and provide flyers to interested women. Study staff will also attend the clinics on days when a large number of prenatal visits are scheduled, and clinic staff will inform them who can be approached as a potential participant. Flyers and posters will also be provided to participating clinics, and participants can self-refer. Participants will be contacted via the method they indicate they prefer.
Participants will attend 6 group meetings lasting 1 hr. every other week. These sessions are aimed at decreasing pregnancy concerns and building coping skills through supportive relationships with experienced local mothers and the other participants in the group. The meetings are closed group sessions.
Participants also receive a "Birth of a Mother" manual designed to guide open discussion during the course of the sessions.
In addition, participants will complete questionnaires at baseline and at the end of the intervention about their mental health, experience of the intervention, and disaster experience.
Conditions
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Study Design
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NA
SINGLE_GROUP
PREVENTION
NONE
Study Groups
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MOMS on the Bayou Intervention Group
Participants complete intervention protocol.
M-O-M-S on the Bayou
Peer and mentor support and meetings across pregnancy
Interventions
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M-O-M-S on the Bayou
Peer and mentor support and meetings across pregnancy
Eligibility Criteria
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Inclusion Criteria
* Below 20 weeks' gestation
* Enrolled in prenatal care
Exclusion Criteria
* 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
18 Years
FEMALE
Yes
Sponsors
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Tulane University
OTHER
Responsible Party
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Locations
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Tulane University
New Orleans, Louisiana, United States
Countries
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Central Contacts
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Facility Contacts
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Emily Harville
Role: primary
Andrea Meyer
Role: backup
Other Identifiers
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2022-1533
Identifier Type: -
Identifier Source: org_study_id
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