Early Screening for PTSD After Unplanned Cesarean Delivery
Predictive Value of Early Peritraumatic Distress Screening for Childbirth-PTSD Following Unplanned Cesarean Delivery
Recruiting
Observational Study
Post Traumatic Stress Disorder
Post Partum Depression
Acute Stress Symptoms
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 19 and older
- Sex
- Female
- Study type
- Observational
- Participants needed
- 420 (estimated)
- Sponsor
- University of British Columbia · Other
Who this trial is looking for
This trial is looking for people who had an unplanned cesarean delivery. Participants will complete surveys after giving birth and again a few weeks later to help predict potential mental health issues related to the experience.
Are You a Good Fit for This Trial?
You may be able to join if
- I am at least 19 years old
- I had an unplanned cesarean delivery
- I can give informed consent
- I can read and understand English questionnaires
You may not be able to join if
- I have experienced fetal or neonatal demise
- I am unable to complete study questionnaires or provide informed consent
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your Eligibility
About This Trial
The goal of this observational study is to learn whether early postpartum screening tools can predict the development of childbirth-related post-traumatic stress symptoms in individuals who undergo unplanned cesarean delivery.
The main questions it aims to answer are:
* Do scores on the Peritraumatic Distress Inventory (PDI) collected 24-48 hours after delivery predict childbirth-related PTSD sy…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age ≥19 years
* Underwent unplanned cesarean delivery
* Able to provide informed consent
* Able to read and understand English questionnaires
Exclusion Criteria:
* Fetal or neonatal demise
* Unable to complete study questionnaires or provide informed consent
Contacts