Skip to content

Mentors Offering Maternal Support (M-O-M-S™): A Prenatal Program for Decreasing Maternal Anxiety and Depression

Mentors Offering Maternal Support (M-O-M-S™): A Prenatal Program Building Maternal Self-Esteem, Coping, and Resilience and Decreasing Depression.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03393637
Acronym
M-O-M-S
Enrollment
1717
Registered
2018-01-08
Start date
2017-12-01
Completion date
2022-03-15
Last updated
2022-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety Fear, Infant, Low Birth Weight, Maternal, Prenatal Depression, Preterm Birth

Keywords

prenatal anxiety, pregnancy, depression, military, intervention

Brief summary

The M-O-M-S project evaluates the effectiveness of the M-O-M-S program for improving birth outcomes and maternal-infant attachment and role satisfaction in a large military sample.

Detailed description

The M-O-M-S project is a longitudinal, multi-site, randomized controlled trial to test program effectiveness for decreasing prenatal maternal anxiety and depression and increasing self-esteem and resilience and assess the relationship to pregnancy complications, birth outcomes, postpartum maternal-infant attachment, role satisfaction and parental stress.

Interventions

BEHAVIORALMentors Offering Maternal Support (M-O-M-S)

10, 1 hour, structured classes meeting every-other-week in person beginning in the first trimester of pregnancy and unlimited access to mentor support.

Sponsors

Joint Program Committee - 5
CollaboratorUNKNOWN
59th Medical Wing
CollaboratorFED
United States Naval Medical Center, San Diego
CollaboratorFED
Madigan Army Medical Center
CollaboratorFED
711th Human Performance Wing
CollaboratorUNKNOWN
University of the Incarnate Word
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Following consent, the participants will randomized to either the treatment or control groups using a computer-generated randomization table developed prior to study start. They will be randomized to either the MOMS intervention or prenatal care without the MOMS. Women randomized to the MOMS program will be assigned to a MOMS group in the first trimester.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Prima or multigravida, first trimester of pregnancy at consent, greater than or equal to 18 years old, active duty, a wife of an active duty service member, or a retiree

Exclusion criteria

* Anticipated permanent change of station during the study (unless going to another one of the study sites or able to complete all treatment components prior to move), dependent daughter of active duty or retired military, greater than 12 weeks gestation at consent, less than 18 years of age and inability to understand English.

Design outcomes

Primary

MeasureTime frameDescription
Postpartum Self-Evaluation Questionnaireassessing change between 1, 3, & 6 months postpartum82-items measuring the woman's perceived postpartum adaptation to motherhood
Family Index Coherenceassessing change between gestational weeks 12, 16, 24, and 32 of pregnancy and 1, 3, & 6 months postpartum17-item instrument measuring the degree to which families feel committed to the military mission and identify a subscale of family coping to manage life changes and stresses
Brief Resilience Scaleassessing change between gestational weeks 12, 16, 24, and 32 of pregnancy and 1, 3, & 6 months postpartum6-item instrument developed to measure the concept of bouncing back from stress.
Lederman Self-Evaluation Questionnaireassessing change between gestational weeks 12, 16, 24, and 32 of pregnancySeven dimensions of pregnancy-specific anxiety
Rosenberg Self-Esteem Scaleassessing change between gestational weeks 12, 16, 24, and 32 of pregnancy and 1, 3, & 6 months postpartum10-item scale measuring the degree to which one values oneself
Family Adaptability and Cohesion Evaluation Scalesassessing change between gestational weeks 12, 16, 24, and 32 of pregnancy and 1, 3, & 6 months postpartum30-item instrument measuring the ability of the family (couple) to change its roles, rules, and power structure.
Edinburgh Postnatal Depression Scaleassessing change between gestational weeks 12, 16, 24, and 32 of pregnancy and 1, 3, & 6 months postpartum10-item scale measuring prenatal or postpartum symptoms of depression
Social Support Indexassessing change between gestational weeks 12, 16, 24, and 32 of pregnancy and 1, 3, & 6 months postpartum17-item scale measuring the extent to which families are integrated into the community, view the community as a source of support, and feel that the community can provide emotional, esteem, and network support

Secondary

MeasureTime frameDescription
Gestational age at birthat first prenatal appointment up to 12 weeksGestational age in weeks at birth determined from last menstrual period (LMP) and/or first trimester ultrasound
Infant birthweightdelivery weight of infant documented at deliveryexact measure obtained from the delivery or infant record of the infants weight at birth in grams

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026