Women who are breastfeeding: Increasing Self-Efficacy to improve outcomes (WISE) Trial
- Conditions
- Breastfeeding exclusivity among primiparous mothers at 6 months postpartumPregnancy and Childbirth
- Registration Number
- ISRCTN85493925
- Lead Sponsor
- Women's College Hospital (Canada)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 956
In-hospital breastfeeding mothers who meet the following criteria:
1. Primiparous
2. Aged above 18 years
3. Singleton birth
4. Infant greater than or equal to 37 weeks gestational age at delivery
5. Can speak and understand English.
1. Maternal/infant health condition that could interfere with breastfeeding (e.g., severe illness, major congenital anomaly)
2. Infant not expected to be discharged home with mother
3. No telephone access
4. Maternal breast reduction surgery
5. Maternal intention to not exclusively breastfeed
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Breastfeeding exclusivity as identified by the Infant Feeding Questionnaire administered at 6 months postpartum
- Secondary Outcome Measures
Name Time Method What is the effect of the breastfeeding self-efficacy intervention (BSEI) on: <br>1. Breastfeeding exclusivity at 3 months postpartum? <br>2. Breastfeeding duration at 3, 6, 9, and 12 months postpartum? <br>3. Breastfeeding difficulties at 3 6, 9, and 12 months postpartum? <br>4. Health service utilization at 3, 6, 9, and 12 months postpartum?<br>5. Cost implications<br>6. Mothers? evaluations of their BSEI and peer support experience<br>7. Nurses? and peers reports of the type and intensity of their BSEI activities