Initial Intervention Efficacy for an Online PTSD Intervention for Pregnant Women
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About
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.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- 18-40 years old
- Fluent in English
Exclusion criteria
- Active and severe domestic violence
- Evidence of a significant mental illness or current substance use disorder that would impede the completion of the intervention
- Suicidal individuals deemed at immediate danger or risk (i.e., requiring immediate hospitalization or treatment)
- Women who smoke
- Women who have a metabolic or endocrine disorder.
Trial design
Primary purpose
Allocation
Interventional model
Masking
5 participants in 1 patient group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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