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临床试验/NCT06918574
NCT06918574已完成不适用

The Effect of Breastfeeding Roadmap on Breastfeeding Self-Efficacy Perception and Breastfeeding Success in Primiparous Women

Selcuk University1 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2025年4月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
74
试验地点
1
主要终点
Sociodemographic characteristics

研究概览

简要总结

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

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •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

排除标准

  • •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

研究组 & 干预措施

Intervention group

Experimental

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.

干预措施: Breastfeeding Education with Breastfeeding Roadmap (Other)

Control group

No Intervention

The control group of the study will receive routine breastfeeding education provided by the clinic's education nurse.

结局指标

主要结局

Sociodemographic characteristics

时间窗: Within the first hour after the mother's birth.

Comparison of sociodemographic characteristics of women before the intervention with the questionnaire

Sociodemographic characteristics

时间窗: Within the first hour after the mother's birth.

Comparison of sociodemographic characteristics of women before the intervention with the questionnaire

Breastfeeding Self-Efficacy Short Form Scale

时间窗: At least two hours before mothers are discharged from the hospital (the discharge period usually varies between 24 and 48 hours)

Post-test data will be collected before mothers are discharged from the hospital (Post-test). The scale consists of 14 items. It is scored between 1-5 and the lowest 14 and the highest 70 points can be obtained. The higher the score obtained from the scale, the higher the breastfeeding self-efficacy.

LATCH Breastfeeding Assessment Tool

时间窗: At least two hours before mothers are discharged from the hospital (the discharge period usually varies between 24 and 48 hours)

Post-test data will be collected before mothers are discharged from the hospital (Post-test). The scale consists of five evaluation criteria and each item is evaluated between 0-2 points. The score that can be obtained from the measurement tool can vary between 0-10. The higher the score obtained from the scale, the higher the breastfeeding success.

Breastfeeding Self-Efficacy Short Form Scale

时间窗: Within the first hour after the mother's birth.

Mothers whose pre-test data are collected will be assigned to intervention and control groups (Pre-test). The scale consists of 14 items. It is scored between 1-5 and the lowest 14 and the highest 70 points can be obtained. The higher the score obtained from the scale, the higher the breastfeeding self-efficacy.

LATCH Breastfeeding Assessment Tool

时间窗: Within the first hour after the mother's birth

Mothers whose pre-test data are collected will be assigned to intervention and control groups (pre-test). The scale consists of five evaluation criteria and each item is evaluated between 0-2 points. The score that can be obtained from the measurement tool can vary between 0-10. The higher the score obtained from the scale, the higher the breastfeeding success.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ebru Bekmezci

PhD

Selcuk University

研究点 (1)

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