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Clinical Trials/NCT06207916
NCT06207916
Completed
N/A

International Survey of Childbirth-Related Trauma - Swedish Part

Region Östergötland1 site in 1 country619 target enrollmentSeptember 1, 2021
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ConditionsChildbirth-related PTSDPTSDPostnatal DepressionFear of ChildbirthPost Traumatic Stress DisorderPostpartum Sadness

Overview

Phase
N/A
Intervention
Not specified
Conditions
Childbirth-related PTSD
Sponsor
Region Östergötland
Enrollment
619
Locations
1
Primary Endpoint
Prevalence of childbirth-related PTSD
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The goal of this cross-sectional observational study is to analyze childbirth-related PTSD, traumatic birth experiences and stress symptoms postpartum. The main questions it aims to answer are:

  • What is the prevalence of traumatic birth experiences, PTSD and stress symptoms in a Swedish postnatal sample?
  • What are the risk factors for postnatal mental ill-health?

Additional goals are to make cross-cultural translations of the instruments City BiTS and Birth Satisfaction Scale - Revised.

Participants will answer an online surveys including several instruments measuring postnatal stress and mental ill-health.

Registry
clinicaltrials.gov
Start Date
September 1, 2021
End Date
January 31, 2022
Last Updated
2 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hanna Grundström

Associate professor

Region Östergötland

Eligibility Criteria

Inclusion Criteria

  • •having given birth 6-16 weeks previously -

Exclusion Criteria

  • •having given birth to a child that did not survive

Outcomes

Primary Outcomes

Prevalence of childbirth-related PTSD

Time Frame: 2022

Study Sites (1)

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