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Initial Intervention Efficacy for an Online PTSD Intervention for Pregnant Women

Post Traumatic Stress Disorder Clinical Trial

Official title:
Initial Intervention Efficacy for an Online PTSD Intervention for Pregnant Women

Clinical Trial Summary

The current study aims to test a brief computer-assisted intervention (psychoeducation + skills) for pregnant women with elevated PTSD symptoms. In this open trial pilot feasibility study, 20 pregnant women in their first trimester will be invited to participate in the study if they endorse elevated PTSD symptoms. Oxytocin and cortisol will be measured at baseline, one month post-intervention, three months post-intervention, and post-delivery to inform the relationship between these hormones, PTSD symptoms, and peripartum/postpartum outcomes. In addition to receiving the psychoeducation + skills intervention during their first trimester, women will be offered a "booster session" intervention following delivery to enhance utilization of skills during a critical period for maternal mental and physical health outcomes.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04264520
Study type Interventional
Source Medical University of South Carolina
Contact
Status Terminated
Phase N/A
Start date June 5, 2020
Completion date April 23, 2021
View Details
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