atchOn: a breastfeeding support study
- Conditions
- BreastfeedingPregnancy and Childbirth
- Registration Number
- ISRCTN14819650
- Lead Sponsor
- niversity College Dublin
- Brief Summary
2021 Protocol article in https://pubmed.ncbi.nlm.nih.gov/34095603/ (added 03/09/2021)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Ongoing
- Sex
- Female
- Target Recruitment
- 220
1. Primiparous women
2. Singleton pregnancy
3. BMI =25 kg/m2 at booking visit
4. 26 – 34 weeks’ gestation at recruitment
5. Aged =18 years
6. Good understanding of English
7. Ability to give informed consent
8. Have a support partner available and willing to participate in the trial if they are randomised to the intervention group. This support partner may be the infant’s father, the pregnant woman’s male or female partner, the pregnant woman’s mother or sister or a friend.
1. Preterm (<37 weeks’ gestation) delivery
2. Any condition requiring medication that is contraindicated for breastfeeding
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method