Weaning
Conditions
Interventions
This is a multicenter, randomized, parallel and open clinical trial. The study will be parallel, as each group of participants will be exposed to only one intervention studied (intervention or control
Sponsors
Universidade Federal do Triângulo Mineiro
Universidade Estadual de Feira de Santana
Universidade Federal do Rio de Janeiro
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Primiparous women; who had a single fetus alive; with gestational age of 37 to 42 weeks; weighing more than 2,500 grams; regardless of the type of delivery; who are hemodynamically stable; conscious and oriented; and hospitalized in the room-ing, of the participating centers, at the time of the allocation for the study.
Exclusion criteria
Exclusion criteria: Will not be included in the postpartum women and neonates with contraindication for breastfeeding; neonates with malformations that prevent or hinder breastfeeding and/or with changes in the mechanics of breastfeeding (lingual frenulum); postpartum women whose neonates were immediately separated after clamping the umbilical cord at birth due to maternal-neonatal complications; postpartum women transferred from other institutions or who have already been discharged (readmission); postpartum women who use illicit and etilist drugs; postpartum women with intellectual and/or sensory disabilities; will be excluded postpartum women which malformations or abnormalities in the mechanics of breastfeeding are detected at the time of allocation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find an increase in the rates of exclusive breastfeeding in the sixth month of life, verified through telephone contact with the postpartum women, from the observation of a variation of at least 5% in the pre- and post-intervention measurements. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find an increase in the rates of exclusive breastfeeding at the time of hospital discharge, measured through an interview with the postpartum woman. ;It is expected to find a reduction in the occurrence of nipple trauma in the first and second week after hospital discharge, measured from the report through telephone contact with the postpartum woman.;It is expected to find an increase in exclusive breastfeeding rates at 1 and 4 months, measured from the report through telephone contact with the participant.;It is expected to find a reduction in the indicative signs of postpartum depression at 1, 4 and 6 months, measured from the report through telephone contact with the participant.;It is expected to find a reduction in hospitalizations and diseases in childhood at 1, 4 and 6 months, measured from the report through telephone contact with the participant.;It is expected to find a reduction in early weaning rates (before the sixth month), measured from the report through telephone contact with the participant. | — |
Countries
Brazil
Contacts
Public ContactMariana Ruiz
Universidade Federal do Triângulo Mineiro
Outcome results
None listed