Evaluating an eHealth Breastfeeding Resource

Status Active, not recruiting

Clinical Trial Summary

This trial will evaluate an eHealth breastfeeding co-parenting resource designed for mothers and their co-parents. Couples will be randomized to study groups and the intervention group will receive information about this resource or the control group will receive usual care. The primary outcomes will be exclusive breastfeeding at 4 and 24 weeks postpartum.

Clinical Trial Description

This trial will evaluate an eHealth breastfeeding co-parenting resource designed for mothers and their co-parents. Couples will be randomized to study groups and the intervention group will receive information about this resource with an online demonstration and weekly emails for 6 weeks reminding them about the resource. The control group will receive usual care and 6 weekly emails reminding them that they are in the study. The primary outcomes will be exclusive breastfeeding at 4 and 24 weeks postpartum. Additional outcomes will include: breastfeeding initiation, duration, challenges, attitude, knowledge, confidence, anxiety, partners support and co-parenting. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03492411
Study type	Interventional
Source	University of Ontario Institute of Technology
Contact
Status	Active, not recruiting
Phase	N/A
Start date	March 25, 2018
Completion date	May 1, 2020

View Details

See also
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