PoursuitAllait: Factors Associated With Continuation of Exclusive Breastfeeding Until the Post-natal Visit

Sponsor
Université de Reims Champagne-Ardenne (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05650684
Collaborator
(none)
100
5.9

Study Details

Study Description

Brief Summary

Breastfeeding promotes the health of mother and her child, and remains the reference in terms of infant nutrition. World Health Organization recommends exclusive breastfeeding for the first six months. This recommended duration is not respected in France with a median duration of breastfeeding in France at 3 months.

Condition or Disease Intervention/Treatment Phase
  • Other: data collection

Detailed Description

The aim is to study factors associated with continuation of exclusive breastfeeding until the post-natal visit.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
Factors Associated With Continuation of Exclusive Breastfeeding Until the Post-natal Visit
Anticipated Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Apr 1, 2023
Anticipated Study Completion Date :
Jul 1, 2023

Arms and Interventions

Arm Intervention/Treatment
"exclusive breastfeeding" group

Women initiating exclusive breastfeeding after birth

Other: data collection
continuation of exclusive breastfeeding until the post-natal visit (6 to 8 weeks after birth)

Outcome Measures

Primary Outcome Measures

  1. breastfeeding [Day 0]

    number of women practicing or not exclusive breastfeeding until postnatal consultation (6 to 8 weeks after birth)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Inclusion Criteria:
  • primiparous and multiparous women

  • women who have initiate breastfeeding

  • women aged 18 and more

  • agreeing to participate in the study

Exclusion Criteria:
  • women whose newborn has been in intensive care unit

  • women with a multiple pregnancy

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Université de Reims Champagne-Ardenne

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Université de Reims Champagne-Ardenne
ClinicalTrials.gov Identifier:
NCT05650684
Other Study ID Numbers:
  • 2022_RIPH_013_Poursuit-Allait
First Posted:
Dec 14, 2022
Last Update Posted:
Dec 16, 2022
Last Verified:
Dec 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Université de Reims Champagne-Ardenne

Study Results

No Results Posted as of Dec 16, 2022