Breastfeeding Roadmap in Primiparous Women

Last updated: May 12, 2025
Sponsor: Selcuk University
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

Breastfeeding Education with Breastfeeding Roadmap

Clinical Study ID

NCT06918574
2024/048
  • Ages > 18
  • Female
  • Accepts Healthy Volunteers

Study Summary

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

Eligibility Criteria

Inclusion

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

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

Study Design

Total Participants: 74
Treatment Group(s): 1
Primary Treatment: Breastfeeding Education with Breastfeeding Roadmap
Phase:
Study Start date:
April 15, 2025
Estimated Completion Date:
August 30, 2025

Study 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 developed 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 at the 1st hour after birth. Pre-test data will collect by the researcher in the patient room within the first hour after birth (before Breastfeeding Roadmap breastfeeding education and hospital breastfeeding education were implemented) by face-to-face interview method.

Post-test; Breastfeeding Self-Efficacy Scale Short-Form, LATCH Breastfeeding Assessment Tool 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.

Connect with a study center

  • Necmettin Erbakan University Faculty of Medicine Hospital

    Konya,
    Turkey

    Active - Recruiting

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