Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
300

Summary

Conditions
  • Breastfeeding
  • Breastfeeding, Exclusive
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: 150 couples will be randomized to group allocation, intervention group or control group with use sequentially numbered opaque envelopesMasking: Single (Outcomes Assessor)Masking Description: Outcome assessor will be blinded to group allocation. Follow up data will be collected via online survey or telephone interview with survey questions. Mode of data collection will depend on participant preferencePrimary Purpose: Prevention

Participation Requirements

Age
Between 18 years and 88 years
Gender
Both males and females

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 t...

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.

Tracking Information

NCT #
NCT03492411
Collaborators
Durham Region Health Department
Investigators
Principal Investigator: Jennifer Abbass-Dick Ms.
About Us
Innovation
Privacy
Terms
Copyright
Get Well Soon © Copyright 2024