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EVA (ECE): Women's Evaluation of the Childbirth Experience: From Pregnancy to Postpartum

Sponsor
Hospices Civils de Lyon (Other)
Overall Status
Completed
CT.gov ID
NCT03687879
Collaborator
(none)
799
Enrollment
26
Locations
3.9
Actual Duration (Months)
30.7
Patients Per Site
7.9
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Women report inappropriate health professional behaviour towards them during pregnancy or childbirth on social networks. However, to date, no data are available to estimate the number of women concerned. These data are necessary to characterize these behaviours to get out of this polemic and build a reflection on the improvement of the patient relationship and the emotional security of women.

Condition or Disease Intervention/Treatment Phase
  • Other: Questionnaires

Study Design

Study Type:
Observational
Actual Enrollment :
799 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Women's Evaluation of the Childbirth Experience: From Pregnancy to Postpartum
Actual Study Start Date :
Sep 17, 2018
Actual Primary Completion Date :
Nov 23, 2018
Actual Study Completion Date :
Jan 13, 2019

Outcome Measures

Primary Outcome Measures

  1. Proportion of women reporting inappropriate behavior [about 1 week]

    An inappropriate behavior, also called "obstetric violence" is defined by medical gestures or acts, speech, embarrassing or hurtful attitudes during pregnancy follow-up or during hospitalization outside childbirth, or during childbirth or immediate after birth. Womens will compleat a questionnaire to report this inappropriate behavior at the exit of the maternity.

  2. Proportion of women reporting inappropriate behavior [at 2 months]

    An inappropriate behavior, also called "obstetric violence" is defined by medical gestures or acts, speech, embarrassing or hurtful attitudes reported by womens with a questionnaire 2 months after exit of the maternity.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:

  • major women

  • who understand french language

Exclusion Criteria:

  • Women refusing to participate

  • having given birth at home

  • whose fetus or newborn has died

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hôpital Privé d'Ambérieu Ambérieu-en-Bugey France 01500
2 Polyclinique du Beaujolais Arnas France 69480
3 CH d'ARDECHE MERIDIONALE Aubenas France 07200
4 CH de BOURG EN BRESSE - Pôle Mère Enfant Bourg-en-Bresse France 01012
5 Centre Hospitalier Pierre Oudot Bourgoin-Jallieu France 38300
6 Clinique St Vincent de Paul Bourgoin-Jallieu France 38300
7 Hôpital Femme Mère Enfant Bron France 69500
8 Centre Hospitalier de Givors Givors France 69700
9 Centre Hospitalier de Villefranche Sur Saône Hôpital Nord-Ouest Gleizé France 69400
10 Hôpital Privé Drôme Ardèche Clinique Pasteur Guilherand-Granges France 07500
11 Réseau AURORE, service de gynécologie Obstétrique, Hôpital de la Croix-Rousse Lyon France 69004
12 Centre Hospitalier St Joseph St Luc Lyon France 69007
13 Hôpital Prive Natecia Lyon France 69008
14 Hôpital de La Croix-Rousse Lyon France 69317
15 Ch Montelimar Ghpp Montélimar France 26200
16 CH du HAUT-BUGEY Oyonnax France 01117
17 Centre Hospitalier Lyon Sud Pierre-Bénite France 69310
18 Polyclinique Lyon Nord Service Maternité (NATECIA) Rillieux-la-Pape France 69140
19 Hôpitaux Drôme Nord - Site de Romans Romans-sur-Isère France 26100
20 Centre Hospitalier de Sainte Foy les Lyon Sainte-Foy-lès-Lyon France 69110
21 Centre Hospitalier de Valence Valence France 26953
22 Clinique de l'Union Vaulx-en-Velin France 69380
23 Ch Vienne Lucien Hussel Vienne France 38209
24 Clinique du Tonkin Villeurbanne France 69100
25 Ghm Les Portes Du Sud Vénissieux France 69200
26 Clinique du Val D'ouest Écully France 69130

Sponsors and Collaborators

  • Hospices Civils de Lyon

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hospices Civils de Lyon
ClinicalTrials.gov Identifier:
NCT03687879
Other Study ID Numbers:
  • 69HCL18_0172
First Posted:
Sep 27, 2018
Last Update Posted:
Aug 15, 2019
Last Verified:
Aug 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:
Problem Behavior

Study Results

No Results Posted as of Aug 15, 2019