The influence of counseling on the duration of exclusive breastfeeding

Phase 3

• Conditions: Clinical Trial, Primary Health Care, Home Assistance, Nursing; V03.175.250; N04.590.233.727; Q65.030

• Registration Number: RBR-37wrrs
• Lead Sponsor: niversidade Federal de Mato Grosso

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-12-27
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Female
• Target Recruitment: Not specified

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

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.

Study & Design

• Study Type: Intervention
• Study Design: Not specified