The evaluation of practices to the binomial mother in the delivery room before and after the Neonatal Resuscitation Course

Not Applicable

• Conditions: Birth Room; ewborn; Permanent Education; Training; C23.550.260.095; O68.0; P01.9

• Registration Number: RBR-2k6jzs
• Lead Sponsor: niversidade Federal de Pernambuco

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-04-22
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

neonates with gestational age greater than or equal to 34 weeks, incluing twins; absence of severe congenital malformation that may lead .

Exclusion Criteria

Mothers with positive serology for imunodeficiency virus (HIV); human limphotrophic T virus( HTLV).

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcome consisted in good practices in the care of the healthy neonate. Late Clamping of the umbilical cord, skin-to-skin contact after birth, and breastfeeding in the first hour of life. This information was obtained through the neonatal records and information obtained from an interview with the mother.It was expected a 10% improvement in good practices after the intervetion.;The primary outcome consisted in good practices in the care of the healthy neonate. Late Clamping of the umbilical cord, skin-to-skin contact after birth, and breastfeeding in the first hour of life. This information was obtained through the neonatal records and information obtained from an interview with the mother. Good practices included breastfeeding in the first hour of life in caesarean births, where there was improvement with statistical significance after the intervention

Secondary Outcome Measures

Name	Time	Method
Secondary outcomes are not expected