Preventing Childbirth-Related PTSD With Expressive Writing
NCT05662423 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 136
Last updated 2026-05-22
Summary
The goal of this clinical trial is to test a brief psychological intervention given to individuals in the first days following childbirth who have experienced a potentially stressful childbirth. The treatment is aimed at preventing post-traumatic stress disorder following childbirth and promoting maternal-infant bonding.
In the days following childbirth, participants will be asked to write about their childbirth experience or a neutral event for three consecutive days, for around 15 minutes each day. Additionally, they will complete a short survey before and after the intervention about their birth experience and mental health. Around 2 months postpartum (with the option of up to around Month 3 PP), participants will take part in mental health and physiological assessments, and in a brief play session with their infant.
Conditions
- PTSD (Childbirth-Related)
Interventions
- BEHAVIORAL
-
Expressive Writing about Childbirth
Participants will write repeatedly about their deepest emotions and thoughts related to their recent childbirth, focusing on the most stressful experiences.
- BEHAVIORAL
-
Neutral Writing
Participants will write repeatedly about neutral daily events/tasks not related to childbirth.
Sponsors & Collaborators
-
Massachusetts General Hospital
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 50 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-11-08
- Primary Completion
- 2026-07-20
- Completion
- 2026-07-31
Countries
- United States
Study Locations
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