Infant Feeding Study.09-68

The recruitment status of this study is unknown because the information has not been verified recently.
Verified November 2010 by Children's Hospital Medical Center, Cincinnati.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
Children's Hospital Medical Center, Cincinnati
ClinicalTrials.gov Identifier:
NCT01233427
First received: November 2, 2010
Last updated: November 11, 2010
Last verified: November 2010

November 2, 2010
November 11, 2010
June 2009
October 2011   (final data collection date for primary outcome measure)
Early lactation difficulties [ Time Frame: 1 year ] [ Designated as safety issue: No ]
a)Estimate the prevalence of early lactation difficulties among the subset of this sample that initiates breastfeeding, b) examine the relationship between metabolic health and lactation difficulties
Early lactation difficulties [ Time Frame: 1 year ] [ Designated as safety issue: No ]
Estimate the prevalence of early lactation difficulties among the subset of this sample that initiates breastfeeding.
Complete list of historical versions of study NCT01233427 on ClinicalTrials.gov Archive Site
Infant feeding attitudes [ Time Frame: 1 year ] [ Designated as safety issue: No ]
describe the prenatal infant feeding attitudes and intentions of a sample of expectant mothers from the same recruitment base as the future intervention trial
Same as current
Not Provided
Not Provided
 
Infant Feeding Study.09-68
The Infant Feeding Experience of New Mothers - a Descriptive Pilot Study.

Characterize a population-based sample of first-time expectant mothers with regards to maternal metabolic health and their infant feeding experience.

The long range purpose of this pilot study is to inform the development of an NIH-funded randomized intervention trial designed to improve early breastfeeding outcomes for mothers planning to breastfeed. The purpose of the pilot study is to 1) described the prenatal infant feeding attitudes and intentions of population-based sample of expectant mothers from the same recruitment base as the future intervention trial, 2) characterize the metabolic health profiles of the sample and 3) estimate the prevalence of early lactation difficulties among the subset of this sample that initiates breastfeeding.

Observational
Observational Model: Cohort
Not Provided
Retention:   Samples Without DNA
Description:

Blood (serum)

Non-Probability Sample

breastfeeding moms

  • Describe the Infant Feeding Attitudes
  • Intentions of a Sample of Expectant First-time Mothers
  • Estimate the Prevalence of Early Lactation Difficulties
Not Provided
Not Provided
Nommsen-Rivers LA, Dolan LM, Huang B. Timing of stage II lactogenesis is predicted by antenatal metabolic health in a cohort of primiparas. Breastfeed Med. 2012 Feb;7(1):43-9. Epub 2011 Apr 27.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
32
October 2011
October 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • First-time expectant mother, speaks English, receiving OB care at designated practice group

Exclusion Criteria:

  • 1) Under 18 years old; 2)no access to local telephone 3) multiple gestation 4) history of major breast surgery
Female
18 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
NCT01233427
09-68
No
Laurie A. Nommsen-Rivers, Cincinnati Children's Hospital Medical Center
Children's Hospital Medical Center, Cincinnati
Not Provided
Principal Investigator: Laurie A Nommsen-Rivers, PhD Children's Hospital Medical Center, Cincinnati
Children's Hospital Medical Center, Cincinnati
November 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP