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NCT03072251 Clinical Trial

Participation of Breast Milk Feeding Mothers in Research

Breastfeeding Clinical Trial

Official title:
Participation of Breast Milk Feeding Mothers in Research

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03072251
Other study ID # PBRC 2017-006
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 5, 2017
Est. completion date October 22, 2018

Study information
Verified date September 2022
Source Pennington Biomedical Research Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To assess concerns and barriers for measuring milk intake of breast fed infants using the remote food photography method and SmartIntake smartphone application. These data will 1) provide support for further development of the Infant RFPM and 2) provide important preliminary data in a National Institutes of Health grant application being developed and assess the prevalence of exclusive breastfeeding and complementary breastfeeding in the study population.

Description:

Study participation will be the completion of an anonymous, online survey powered by HIPAA compliant REDCap database. The survey will be made available to potential participants through the internet. The survey will take approximately five minutes to complete. The expected duration of recruitment and completion of the study is six months.

Recruitment information / eligibility
Status Completed
Enrollment 570
Est. completion date October 22, 2018
Est. primary completion date October 22, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Any individual may take the survey. Exclusion Criteria: - None

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Pennington Biomedical Research Center Baton Rouge Louisiana

Sponsors (1)
Lead Sponsor Collaborator
Pennington Biomedical Research Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Other Prevalence of breastfeeding in the survey population (exclusive, in combination with infant formula, in combination with other foods) Outcome measured by questionnaire 1 day
Other Method of feeding (breast, expressed human milk in an infant feeding bottle, combination of feeding methods) Outcome measured by questionnaire 1 day
Primary Receptivity for measuring milk intake for 5-7 days using a smartphone app Outcome measured by questionnaire 1 day
Secondary Receptivity for expressing human breast milk to assess milk intake for 5-7 days Outcome measured by questionnaire 1 day
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