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Protocol to Support Breastfeeding for Postpartum Women and Mothers of Babies With Congenital Heart Disease

Congenital Heart Disease Clinical Trial

Official title:
Support Protocol for Face-to-face and Teleservice Breastfeeding for Puerperal Women and Mothers of Babies With Congenital Heart Disease: a Randomized Clinical Trial

Clinical Trial Summary

To evaluate the effect of applying a hybrid protocol (face-to-face and via call center) of breastfeeding assistance and guidance on the duration of breast milk supply to babies with congenital heart disease for 6 months.

Clinical Trial Description

The objective of this randomized, multicenter clinical trial is to evaluate the effect of applying a hybrid protocol (face-to-face and telemarketing) of assistance and guidance on breastfeeding and duration of breast milk supply for infants with congenital heart disease in the first 6 months of life. Recruitment of infants diagnosed with congenital heart disease occurs within the first 72 hours of life, being followed up for 6 months. Initially, the mothers in the control group, as well as the mothers in the intervention group, receive a booklet with guidelines on breastfeeding, a standardized measuring cup for milk collections and a breastfeeding booklet. In addition, mothers in the intervention group receive monthly videos with guidance on breastfeeding, monthly consultations with a breastfeeding consultant and a support group via whatsapp with the researcher and scientific initiation student until the baby is 6 months old. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06025864
Study type Interventional
Source Instituto de Cardiologia do Rio Grande do Sul
Contact Juliana Caprini, Esp
Phone (54)992044907
Email juli_caprini@yahoo.com
Status Recruiting
Phase N/A
Start date July 1, 2022
Completion date February 20, 2024
View Details
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