The prevalence of posttraumatic stress disorder in pregnancy and after birth: A systematic review and meta-analysis.
Pelin Dikmen Yildiz, Susan Ayers, Louise Phillips
https://pubmed.ncbi.nlm.nih.gov/27865585Actively Recruiting
Led by Massachusetts General Hospital · Updated on 2026-05-22
136
Participants Needed
1
Research Sites
1 weeks
Total Duration
Researchers are investigating a brief psychological intervention aimed at preventing post-traumatic stress disorder (PTSD) related to childbirth and promoting bonding between mothers and their infants. This study focuses on women who have recently experienced a potentially stressful childbirth and are at risk for developing childbirth-related PTSD (CB-PTSD). Since no recommended interventions currently exist for this condition in U.S. hospitals, this research seeks to fill that gap by testing a low-cost, feasible approach. Participants will be randomly assigned to one of two groups. One group will write about their recent childbirth experience, focusing on their deepest emotions and thoughts related to the most stressful aspects. The other group will write about neutral daily events unrelated to childbirth. Writing sessions will occur for three consecutive days, about 15 minutes each day. Assessments including surveys about birth experience and mental health will be completed before and after the intervention. Around two months postpartum, participants will undergo mental health and physiological evaluations and participate in a brief play session with their infant. Throughout the study, researchers will measure changes in PTSD symptoms using standardized checklists before and after the intervention and at two months postpartum. They will also assess maternal-infant bonding through various scales and observational assessments, as well as monitor physiological responses related to traumatic memory recall. The total participation includes the initial writing sessions, surveys, and follow-up assessments up to about three months postpartum, with safety and mental health carefully monitored during this period.
CONDITIONS
Preventing Childbirth-Related PTSD With Expressive Writing
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Within a few days postpartum
Participants write repeatedly about their recent childbirth or neutral daily events to assess the effects of expressive writing on postpartum mental health.
1 baseline visit and 1 follow-up visit within 1 day of treatment
Duration - Up to around 3 months postpartum
Participants continue to be observed for mental health and bonding outcomes up to around Month 3 postpartum.
Approximately 1 visit at Month 2 postpartum
Total: 1 location
1
Massachusetts General Hospital
Boston, Massachusetts, United States, 02129
Actively Recruiting
S
Sharon Dekel, Ph.D. M.Phil., M.S.
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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