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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04487171
Other study ID # PI2020_843_0049
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 21, 2020
Est. completion date August 2023

Study information

Verified date March 2023
Source Centre Hospitalier Universitaire, Amiens
Contact Arthur FOULON, MD
Phone (33)322087382
Email foulon.arthur@chu-amiens.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Postpartum depression (PPD) represent around 15% of birth in developed countries. The context of the COVID-19 epidemy represents a possible source of additional emotional distress. The objective of this study is to determine the screening prevalence and risk factors of postpartum depression, among women who deliver in fourth hospital in the North of France in the context of the COVID epidemy.


Recruitment information / eligibility

Status Recruiting
Enrollment 248
Est. completion date August 2023
Est. primary completion date July 2023
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Single baby delivery - alive new born child without admission in neonatal intensive care unit - French-speaking mother - mother older than 18 years old Exclusion Criteria: - Patients who refuses the inclusion

Study Design


Intervention

Other:
Questionnaire
The mothers were administrated three questionnaires, (i) the Edinburgh Postnatal Depression Scale (EPDS), (ii) the State-Trait Anxiety Inventory (STAI-YA), and (iii) the Mother-to-Infant Bonding Scale (MIBS) in two stages, on days 2-3 after delivery and during a phone call between days 25-35.

Locations

Country Name City State
France CHU Amiens Amiens

Sponsors (4)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens Central Hospital Saint Quentin, Centre Hospitalier Compiègne, Centre Hospitalier de Beauvais

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Variation of prevalence of clinically-significant post-partum depressive symptoms Variation of prevalence of clinically-significant post-partum depressive symptoms up to 35 days after delivery
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