MedTrace Logo

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

NCT04160273 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1451

Last updated 2025-07-25

No results posted yet for this study

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.

Conditions

  • Delivery
  • Post Partum

Interventions

DIAGNOSTIC_TEST

patient questionnaire and telephone follow-up

PDI scale is filled in before returning home and follow-up at one month and one year thanks to a telephone call during which the patient answers the PCL-S questionnaire

Sponsors & Collaborators

  • University Hospital, Angers

    lead OTHER_GOV

Principal Investigators

  • Guillaume LEGENDRE, MDPhD · University Hospital, Angers

Study Design

Allocation
NA
Purpose
SCREENING
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-05
Primary Completion
2024-03-05
Completion
2025-03-12

Countries

  • France

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04160273 on ClinicalTrials.gov