Facilitation and Barriers to Breastfeeding in the NICU
1 other identifier
observational
8
0 countries
N/A
Brief Summary
To date, there is a paucity of research focusing on maternal breastfeeding goals, how these goals may change after an unexpected event such as a preterm birth, and how mothers of ill and preterm infants define breastfeeding success. No studies were identified that focused exclusively on the breastfeeding goals of mothers of hospitalized preterm infants The purpose of this study is to answer the following research questions: 1) What are the breastfeeding goals of mothers with preterm infants in the NICU? and 2) What are mothers' perceptions of facilitators and barriers to meeting their breastfeeding goals in the NICU?
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Sep 2007
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2007
CompletedFirst Submitted
Initial submission to the registry
September 10, 2007
CompletedFirst Posted
Study publicly available on registry
September 11, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2008
CompletedJune 9, 2008
June 1, 2008
September 10, 2007
June 6, 2008
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- have one (or more) infant(s) currently admitted in the NICU at the RVH;
- intended to provide breast milk to their infant(s);
- are able to speak English; and
- are willing to be audiotaped during the interview.
You may not qualify if:
- Include mothers who:
- never intended to breastfeed;
- have high risk social situations (for example, known maternal mental illness; involvement of youth protection; known alcohol and drug abuse; adoption; identified congenital anomalies);
- gave birth at term; and
- have infants with significant birth defects or serious medical conditions in addition to prematurity.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Luisa Ciofani, RN, M.Sc.(A)
McGill Univsersity Health Centre
Study Design
- Study Type
- observational
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
September 10, 2007
First Posted
September 11, 2007
Study Start
September 1, 2007
Study Completion
April 1, 2008
Last Updated
June 9, 2008
Record last verified: 2008-06