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Women who are breastfeeding: Increasing Self-Efficacy to improve outcomes (WISE) Trial

A randomised controlled trial to evaluate the effect of a breastfeeding self-efficacy enhancing intervention on breastfeeding exclusivity among primiparous mothers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN85493925
Enrollment
956
Registered
2013-07-26
Start date
2014-01-31
Completion date
Unknown
Last updated
2018-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breastfeeding exclusivity among primiparous mothers at 6 months postpartum Pregnancy and Childbirth

Interventions

Current interventions as of 19/01/2018: Participants allocated to the intervention group will receive standard postpartum care plus four individualized self-efficacy enhancing sessions with a trained
mothers will also be offered telephone-based peer support following hospital discharge up to 18 months postpartum. Previous interventions: Participants allocated to the intervention group will receiv
mothers will also be offered telephone-based peer support following hospital discharge up to 12 months postpartum.

Sponsors

Women's College Hospital (Canada)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 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.

Exclusion criteria

Exclusion criteria: 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

Design outcomes

Primary

MeasureTime frame
Breastfeeding exclusivity as identified by the Infant Feeding Questionnaire administered at 6 months postpartum

Secondary

MeasureTime frame
What is the effect of the breastfeeding self-efficacy intervention (BSEI) on: 1. Breastfeeding exclusivity at 3 months postpartum? 2. Breastfeeding duration at 3, 6, 9, and 12 months postpartum? 3. Breastfeeding difficulties at 3 6, 9, and 12 months postpartum? 4. Health service utilization at 3, 6, 9, and 12 months postpartum? 5. Cost implications 6. Mothers? evaluations of their BSEI and peer support experience 7. Nurses? and peers reports of the type and intensity of their BSEI activities

Countries

Canada

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026