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Clinical Trials/NCT04160273
NCT04160273
Completed
N/A

Evaluation of Postpartum Posttraumatic Stress Disorder at Angers University Hospital (ESPT-PP)

University Hospital, Angers1 site in 1 country1,451 target enrollmentMarch 5, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Delivery
Sponsor
University Hospital, Angers
Enrollment
1451
Locations
1
Primary Endpoint
The risk of PTSD at 1 month is detected using the PCL-S scale.
Status
Completed
Last Updated
9 months ago

Overview

Brief Summary

The purpose of this study is to estimate the prevalence of post-traumatic stress disorder (PTSD) at one month in women who have given birth at the University Hospital of Angers over a period of 1 year.

Detailed Description

Childbirth is a natural process expected, prepared and imagined by all future parents. A traumatic experience of childbirth and its consequences is a major problem that is often underestimated for women's health. Some women may develop Post Traumatic Stress Disorder (PTSD) after delivery. The literature reports a prevalence of PTSD in relation to childbirth of 1.3 to 6%. Symptoms of post-traumatic stress can be triggered by any event, perceived as threatening to the life or physical integrity of the person or a third party and causing intense fear, helplessness and horror. It may be thought that childbirth, by its psychological and physiological characteristics, can be described as an extreme experience and its experience depends on multiple factors. Thus, an innocent childbirth for caregivers can be traumatically experienced by the woman. The symptoms described are symptoms of avoidance (inability to return to the scene of trauma, denial of trauma), symptoms of intrusion (nightmares, reviviscences) and symptoms of neuro-vegetative hyper activation (sleep disorders, anger, emotional indifference ). The development of PTSD following childbirth is a known phenomenon, but minimized and very little diagnosed by obstetric teams. Therefore, it seems interesting to assess the prevalence of PTSD during childbirth in order to optimize our management, that is to identify patients at risk of PTSD and offer them adapted psychological follow-up. This study also aims to describe the kinetics of the development of post-traumatic postpartum symptoms and to study the risk factors for the development of PTSD.

Registry
clinicaltrials.gov
Start Date
March 5, 2021
End Date
March 12, 2025
Last Updated
9 months ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
University Hospital, Angers
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Major and francophone patient,
  • Giving birth (≥ 37 weeks of amenorrhea) to the maternity hospital of Angers University Hospital,
  • Agree to participate in the study (signature of consent).

Exclusion Criteria

  • Birth of a child born lifeless,
  • Patient deprived of liberty by judicial or administrative decision,
  • Patient subject to a legal protection measure,
  • Patient unable to express her consent.

Outcomes

Primary Outcomes

The risk of PTSD at 1 month is detected using the PCL-S scale.

Time Frame: 1 Month

The risk of PTSD at 1 month is detected using the PCL-S scale. Patients are considered at high risk if they have a score ≥ 26 on this scale. A consultation with a psychiatrist is offered to these patients at risk of PTSD in order to make the diagnosis and offer them appropriate care if necessary.

Secondary Outcomes

  • Detect a state of post-traumatic stress(1 Month and 1 year)
  • Determine the emotional distress of a person at the time of a traumatic event at 1 month and one year(1 month and 1year)
  • Collect the risk factors associated with PTSD(5 Days)

Study Sites (1)

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