Clinical Trial, Primary Health Care, Home Assistance, Nursing
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: GESTANT: That intends to breastfeed; That you accept to participate in the research in prenatal and later in the puerperium. PUERPERA AND NEWBORN: Puerper who participated in the research since the gestation; That the delivery occurred with Gestational Age (GI) equal to or greater than 37 weeks; Newborn with birth weight equal to or greater than 2,500 g.
Exclusion criteria
Exclusion criteria: PREGNANT: Multiple gestation; Child donation plans; Mental restrictions that make it impossible to understand the instrument; Important clinical settings in which breastfeeding is contraindicated (HIV, HTLV, use of illicit narcotic substances, etc.). PUERPERA AND NEWBORN: Change of residence of the area of coverage of the Family Health Strategy that belonged to the gestation; Childbirth and / or postpartum with important obstetric complications that make breastfeeding difficult (severe hemorrhage, etc.); Congenital malformations of newborns that may contraindicate or complicate breastfeeding; newborn sent to the Neonatal Intermediate Care Unit, Neonatal Intensive Care Unit, or equivalent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome measure will be exclusive breastfeeding from birth to the child's 120 days of life, collecting data longitudinally during this period. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome measure will be the duration of any breastfeeding from birth to the child's 120 days of life, collecting the data longitudinally during that period | — |
Countries
Brazil
Contacts
EVELINE AMOR DIVINO