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Facilitation and Barriers to Breastfeeding in the NICU

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00527956
First Posted: September 11, 2007
Last Update Posted: June 9, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
McGill University Health Center
  Purpose

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?


Condition
Breastfeeding Prematurity

Study Type: Observational
Study Design: Time Perspective: Prospective

Resource links provided by NLM:


Further study details as provided by McGill University Health Center:

Estimated Enrollment: 8
Study Start Date: September 2007
Study Completion Date: April 2008
Detailed Description:
As the objective of this study is to describe the breastfeeding goals of mothers and their perceptions of breastfeeding support in the NICU, this study will follow a descriptive, qualitative design. Mothers of preterm newborns in the Royal Victoria Hospital will participate in a semi-structured interview about their breastfeeding goals and what they perceived to be facilitators and barriers to achieving their intended goals. During the interviews, the mothers will be asked a set of socio-demographic questions, open-ended questions about their breastfeeding goals, and open-ended questions about their perceptions of barriers and facilitators to meeting these goals in the NICU Participants may also receive one follow-up phone call to clarify their responses to the questions or to validate the information obtained from the interview.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 50 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. have one (or more) infant(s) currently admitted in the NICU at the RVH;
  2. intended to provide breast milk to their infant(s);
  3. are able to speak English; and
  4. are willing to be audiotaped during the interview.

Exclusion Criteria:

Include mothers who:

  1. never intended to breastfeed;
  2. have high risk social situations (for example, known maternal mental illness; involvement of youth protection; known alcohol and drug abuse; adoption; identified congenital anomalies);
  3. gave birth at term; and
  4. have infants with significant birth defects or serious medical conditions in addition to prematurity.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00527956


Sponsors and Collaborators
McGill University Health Center
Investigators
Principal Investigator: Luisa Ciofani, RN, M.Sc.(A) McGill Univsersity Health Centre
  More Information

ClinicalTrials.gov Identifier: NCT00527956     History of Changes
Other Study ID Numbers: PSY 07-009
First Submitted: September 10, 2007
First Posted: September 11, 2007
Last Update Posted: June 9, 2008
Last Verified: June 2008

Keywords provided by McGill University Health Center:
Breastfeeding premature infants