Breastfeeding Failure: Influence of Smartphone Use and Distraction Factors (BRIEFCALL)

September 5, 2023 updated by: Centre Hospitalier Universitaire, Amiens

The benefits of breastfeeding no longer need to be proven. Many studies have shown its positives effects on both infants and mothers. Exclusive breastfeeding is thus recommended within the first six months of life.

Excessive screen use has been shown to be harmful in many aspects of daily life. The impact upon the relation between mother and newborn infant is poorly studied.

The study aims to evaluate the impact of the use of smartphones on the success and duration of breastfeeding.

Study Overview

Status

Recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • France
    • Picardie
      • Amiens, Picardie, France, 80054

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

breastfeeding mothers of Newborn breastfed infant born in the maternity ward of the Amiens-Picardie University Hospital

Description

Inclusion Criteria:

  • breastfeeding mothers of Newborn breastfed infant born in the maternity ward of the Amiens-Picardie University Hospital

Exclusion Criteria:

  • Mother refusing to participate in the study; hospitalization during the neonatal period

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
breastfeeding success (Yes)
Mothers are to be contacted at 1 month to assess the main outcome: breastfeeding status (Yes vs No) classified as breastfeeding success (Yes) or breastfeeding failure (No).
breastfeeding failure (No)
Mothers are to be contacted at 1 month to assess the main outcome: breastfeeding status (Yes vs No) classified as breastfeeding success (Yes) or breastfeeding failure (No).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Variation of Breastfeeding status in both groups
Time Frame: at 2 months
At 2 months after birth, mothers will be contacted to record their breastfeeding status.
at 2 months
Variation of Breastfeeding status in both groups
Time Frame: at 3 months
At 3 months after birth, mothers will be contacted to record their breastfeeding status.
at 3 months
Variation of Breastfeeding status in both groups
Time Frame: at 4 months
At 4 months after birth, mothers will be contacted to record their breastfeeding status.
at 4 months
Variation of Breastfeeding status in both groups
Time Frame: at 6 months
At 6 months after birth, mothers will be contacted to record their breastfeeding status.
at 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Centre Hospitalier Universitaire, Amiens

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 2, 2023

Primary Completion (Estimated)

December 1, 2023

Study Completion (Estimated)

June 1, 2024

Study Registration Dates

First Submitted

June 13, 2023

First Submitted That Met QC Criteria

June 13, 2023

First Posted (Actual)

June 23, 2023

Study Record Updates

Last Update Posted (Estimated)

September 6, 2023

Last Update Submitted That Met QC Criteria

September 5, 2023

Last Verified

September 1, 2023

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • PI2023_843_0061

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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