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临床试验/NCT06775444
NCT06775444尚未招募不适用

The Effect Of The Theory Of Planned Behavior Based Breastfeeding Education Program Given To Pregnant Women On Breastfeedıng Adaptation, Motivation, Self-Efficacy And The Tendency To Early Weaning.

Ankara University0 个研究点目标入组 88 人开始时间: 2025年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
88
主要终点
Breastfeeding Attrition Prediction Tool (BAPT)

研究概览

简要总结

The aim of the research is to examine the effect of a breastfeeding training program based on the theory of planned behavior on Pregnant Womens' Breastfeeding Adaptation, Motivation, Self-Efficacy And The Tendency To Early Weaning.

详细描述

The aim of the study is to examine the effects of a breastfeeding education program based on the theory of planned behavior on breastfeeding adaptation, motivation, self-efficacy, and the tendency to stop breastfeeding.

The study was planned to be conducted as a single-center, parallel group, randomized controlled experimental, prospective study in a pretest-posttest design.

The study was planned to be conducted in the pregnancy school/breastfeeding counseling polyclinic of Düzce Atatürk State Hospital. The sample of the study will consist of pregnant women in the last trimester who meet the inclusion criteria. Considering the losses that may occur during the study process, it is planned to continue the study with a total of 88 pregnant women.

The data of the study will be collected from the patient based on the "Introductory Information Form", "Information Form Regarding Birth and Breastfeeding Process", "Breastfeeding Adaptation Scale", "Breastfeeding Motivation Scale (For Primiparous Mothers)", "Breastfeeding Motivation Scale (For Multiparous Mothers)", "Antenatal Breastfeeding Self-Efficacy Scale-Short Form", "Breastfeeding Self-Efficacy Scale-Short Form", "Breastfeeding Discontinuity Scale" and "Breastfeeding Follow-up Form".

In the study, the "Breastfeeding Education Program Based on Planned Behavior Theory" consisting of 2 sessions will be applied to the intervention group, while the routine breastfeeding education in the hospital where the study is conducted will be applied to the control group. The breastfeeding process will be followed for 6 months after birth in both groups.

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
Double (Participant, Outcomes Assessor)

盲法说明

In order to ensure confidentiality in the group distributions, the block randomization assignment of the intervention and control groups will be made by someone outside the research and will be received in pre-prepared opaque envelopes. A separate envelope will be prepared for each pregnant woman participating in the research and she will be asked to choose one. Pregnant women will not know which group they are in. Since the researcher will also be the implementer of the application, blinding will not be possible for the groups that the pregnant women are in. For this reason, only participant and statistician blinding will be provided in the study.

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

  • •Those who are over 18 years old
  • •Pregnant women in their last trimester (pregnant women who are 27 weeks or more)
  • •Those who receive breastfeeding training at the Pregnancy School
  • •Speak and understand Turkish
  • •Do not have a risky pregnancy diagnosis
  • •Do not have multiple pregnancies
  • •Do not have a psychiatric or neurological disease that will affect their cognitive functions
  • •Have the WhatsApp application on their phone
  • •Volunteer to participate in the research
  • •Want to breastfeed their baby
  • •Have given birth at >37 weeks of pregnancy
  • •Have a baby weighing at least 2500 grams
  • •Have a single healthy baby in the postpartum period
  • •Mothers who do not have breast problems that prevent breastfeeding, do not use medication that passes into breast milk, or have any disease (such as active tuberculosis, HIV) were determined as follows.

排除标准

  • •Those who could not continue the study for any reason
  • •Those who did not participate in all final tests
  • •Those who did not participate in all training
  • •Those who could not be reached more than 5 times in each planned telephone/face-to-face meeting.
  • •Those whose babies were hospitalized in neonatal intensive care after birth (except for babies hospitalized for more than 24 hours - due to neonatal jaundice)

研究组 & 干预措施

Intervention Group

Active Comparator

In addition to the routine breastfeeding training in the hospital where the study was conducted, the intervention group will be given a 2-session "Breastfeeding Education Program Based on the Theory of Planned Behavior".

干预措施: Breastfeeding Education Program Based on Planned Behavior Theory (Behavioral)

Control group

Sham Comparator

The control group will receive routine breastfeeding training at the hospital where the study is conducted.

干预措施: Routine Breastfeeding Training (Behavioral)

结局指标

主要结局

Breastfeeding Attrition Prediction Tool (BAPT)

时间窗: Pre-test application after routine breastfeeding education, Post-test application after the Breastfeeding Education Program Based on Planned Behavior Theory, 7-14 days postpartum, 4-6 weeks postpartum, 4th month postpartum, Postpartum 6th month

Breastfeeding Attrition Prediction Tool (BAPT) is a scale consisting of 90 questions on a 5-point Likert-type scale based on the theory of planned behavior. There are four different sub-dimensions in the scale, which does not have a total score. These are "Negative Breastfeeding Attitude", "Positive Breastfeeding Attitude", "Social and Professional Support" and "Breastfeeding Control" and each sub-scale is scored separately. A high scale score indicates that the mother has high breastfeeding control.

次要结局

  • Breastfeeding Self-Efficacy Scale Short Form (Antenatal Breastfeeding Self-Efficacy Scale)(1. A pre-test will be applied before the Breastfeeding Education Program Based on Planned Behavior Theory. 2. Postpartum 7-14 days 3. Postpartum 4-6 weeks 4. Postpartum 4th month 5. Postpartum 6th month)
  • Breastfeeding Adaptation Scale (BFAS)(7-14 days postpartum)
  • Breastfeeding Motivation Scale (For Primiparous Mothers)(1.Postpartum 7-14 days, 2. Postpartum 4-6 weeks, 3. Postpartum 4th month, 4. Postpartum 6th month)
  • Breastfeeding Motivation Scale (For Multiparous Mothers)(1.Postpartum 7-14 days, 2. Postpartum 4-6 weeks, 3. Postpartum 4th month, 4. Postpartum 6th month)
  • Breastfeeding Tracking Form(1. The first 48 hours after birth, 2.Postpartum 7-14 days, 3. Postpartum 4-6 weeks, 4. Postpartum 4th month, 5. Postpartum 6th month)

研究者

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

Aylin Tozluoğlu

MSc

Ankara University

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