Breastfeeding Roadmap in Primiparous Women

Selcuk University

Status

Completed

Conditions

Self Efficacy

Breastfeeding

Treatments

Other: Breastfeeding Education with Breastfeeding Roadmap

Study type

Interventional

Funder types

Other

Identifiers

NCT06918574

2024/048

Details and patient eligibility

About

The effect of the breastfeeding roadmap used in primiparous mothers on breastfeeding self-efficacy perception and breastfeeding success will be evaluated.

Full description

The research was planned as a randomized controlled experimental study. Mothers who meet the inclusion criteria and agree to participate in the study will be assigned to the intervention and control groups according to the randomization list.

A total of 74 primiparous mothers who gave birth, 37 in the intervention group and 37 in the control group, will be included in the study.

In addition to the routine breastfeeding education given by the clinic's education nurse, the mothers in the intervention group will also receive a "Breastfeeding Roadmap" education poster prepared by the researchers, which will be hung on the wall of their rooms. The researcher will introduce the Breastfeeding Roadmap to the mothers and provide information on breastfeeding. Routine hospital breastfeeding education will receive to mothers in the control group after childbirth.

Data Collection Pre-Test; Introductory Information Form, Breastfeeding Self-Efficacy Scale Short-Form, LATCH Breastfeeding Assessment Tool will be collected within the first hour after birth (before Breastfeeding Roadmap breastfeeding education and hospital routine breastfeeding education were implemented) Post-test; Breastfeeding Self-Efficacy Scale Short-Form, LATCH Breastfeeding Assessment Tool will be collected at least two hours before mothers are discharged from the hospital (the discharge period usually varies between 24 and 48 hours).

At the end of the study, the results of the mothers in the experimental and control groups will be evaluated.

Enrollment

74 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Volunteer to participate in the study,
Primiparous,
Giving birth at 37 weeks of gestation or later,
No condition preventing breastfeeding,
No condition preventing breastfeeding in the baby,
At least primary school graduate,
Mothers aged 18 and over

Exclusion criteria

Those who have given birth to multiple pregnancies,
Those who received general anesthesia for Caesarean section,
Those who have any chronic disease, diagnosed mental or psychiatric illness history,
Those who have a history of preeclampsia, eclampsia and gestational diabetes,
Those whose babies are in intensive care after birth