Facilitation and Barriers to Breastfeeding in the NICU

Breastfeeding Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00527956
• Other study ID #: PSY 07-009
• Status: Completed
• Phase: N/A
• First received: September 10, 2007
• Last updated: June 6, 2008
• Start date: September 2007
• Est. completion date: April 2008

Study information

• Verified date: June 2008
• Source: McGill University Health Center
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada: Ethics Review Committee
• Study type: Observational

Clinical Trial 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?

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 8
• Est. completion date: April 2008
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 50 Years

Eligibility

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.

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

• Breastfeeding
• Prematurity

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
McGill University Health Center