Telemonitoring to improve maternal confidence in breastfeeding

Not Applicable

• Conditions: breastfeeding; early weaning; F01.145.407.199; F01.752.747.792.700

• Registration Number: RBR-7m7vc8
• Lead Sponsor: Departamento de Enfermagem da Universidade Federal do Ceará

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-06-27
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Data analysis completed
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Women in the immediate puerperal period, considered the period between the first and tenth day after childbirth;
Puerperas with at least six hours postpartum, since before that moment it would be inopportune to perform data collection, judging that the first hours after childbirth are characterized by emotional stress for the mother, making it even more difficult due to the physiological changes that occur;
Single term full term puerperal women (gestational age ? 37 weeks, <41 weeks), since the clinical conditions and the environment in which the preterm newborn is hospitalized are factors that may hinder breastfeeding, in addition to that in some situations it is necessary to initiate the use of milk formulas in the child's diet;
Bereaved children 12 years of age or over, considering the Statute of the Child and Adolescent, Law No. 8,069 / 90;
Puerperas with newborns hospitalized in joint housing;
Puerperas that are practicing the AM;
Puerperas who have at least one telephone contact.

Exclusion Criteria

Puerperas who declared their intention not to breastfeed;
Puerperas with age <12 years or> or equal to 60 years;
Puerperas that presented clinical intercurrences at the time of data collection (heart disease, nephropathy, diabetes, hypertension, among others);
Women with obstetric complications in the puerperal period (anemia, transvaginal bleeding, post-rachidial headache, among others);
Puerperas that presented some type of contraindication to breastfeeding (Acquired Immunodeficiency Syndrome, chemical dependency, among others);
Puerperas with mental restrictions that precluded the understanding of the instrument;
Puerperas who performed breast reduction or who had breast augmentation because, although these procedures do not contraindicate breastfeeding, in general, women who undergo breast reduction may decide not to breastfeed;
Puerperas with children hospitalized in the intensive care unit, judging that the sector is home to newborns with critical clinical conditions that may make breastfeeding impossible;
Puerperas whose children were born with disabilities that prevented or hindered breastfeeding (cleft palate, atresia of the esophagus, among others);
Puerperas with hearing impaired.

Study & Design

• Study Type: Intervention
• Study Design: Not specified