Evaluation of the Effectiveness of a Breastfeeding Education Program Based on Planned Behavior Theory

Ankara University

Status

Not yet enrolling

Conditions

Breast Feeding

Treatments

Behavioral: Breastfeeding Education Program Based on Planned Behavior Theory

Behavioral: Routine Breastfeeding Training

Study type

Interventional

Funder types

Other

Identifiers

NCT06775444

AnkaraÜ-HF-AT-01

Details and patient eligibility

About

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.

Full description

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.

In the analysis of the study, it is planned to analyze descriptive statistics (number, percentage, mean and standard deviation), significance test of the difference between two means in independent groups (t test), t test in dependent groups, multi-way and one-way variance analysis in repeated measurements, Pearson correlation analyses for the relationships between the dimensions determining the scale levels, and the chi-square homogeneity test for whether the intervention and control groups are homogeneous in terms of characteristics.

Enrollment

88 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

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.

Exclusion criteria

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)

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

88 participants in 2 patient groups

Intervention Group

Active Comparator group

Description:

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".

Treatment:

Behavioral: Breastfeeding Education Program Based on Planned Behavior Theory

Control group

Sham Comparator group

Description:

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

Treatment:

Behavioral: Routine Breastfeeding Training