Breastfeeding
Conditions
Interventions
This is a randomized clinical trial, where randomization will be performed using Microsoft Excel software with the "0 or 1" command, where 0 corresponds to the Control Group (n = 84) and 1 to the Inte
I02.233.332
Sponsors
Empresa Brasileira de Serviços Hospitalares - EBSERH
Universidade Federal de Alagoas
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Puerperal women over the age of 18; who can read and write; have access to the WhatsApp platform; have been discharged from the hospital with their child
Exclusion criteria
Exclusion criteria: Puerperal women who were separated from their children for any reason during the study; who had illnesses contraindicating breastfeeding – HIV positive and Chagas disease ; who had premature conceptions or congenital problems such as cerebral palsy, microcephaly, or malformation of the digestive, cardiovascular, and oral cavity systems (factors that hinder the breastfeeding process)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| An increase in the prevalence of exclusive breastfeeding is expected in the control group when compared to the intervention group, through participatory education strategies for the promotion and encouragement of breastfeeding. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected. | — |
Countries
Brazil
Contacts
Public ContactMyrtis Bezerra
Universidade Federal de Alagoas
Outcome results
None listed