Recruitment

Recruitment Status
Recruiting

Summary

Conditions
  • Anxiety Fear
  • Infant, Low Birth Weight
  • Maternal
  • Prenatal Depression
  • Preterm Birth
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention 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.Masking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Only males

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-i...

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.

Tracking Information

NCT #
NCT03393637
Collaborators
  • Joint Program Committee - 5
  • 59th Medical Wing Science and Technology
  • United States Naval Medical Center, San Diego
  • Madigan Army Medical Center
  • 711th Human Performance Wing
Investigators
Principal Investigator: Karen L Weis, PhD University of the Incarnate Word