- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05666817
The Effect of Postpartum Breastfeeding Education on Breastfeeding Self-efficacy and Breastfeeding Success
The Effect of Postpartum Breastfeeding Education Given to Women Who Had Normal Vaginal and Cesarean Delivery on Breastfeeding Self-efficacy and Breastfeeding Success
Objective: This study will be conducted as a pre-test post-test randomized controlled study in order to determine the effect of postpartum breastfeeding education given to women who had normal vaginal delivery and cesarean section on breastfeeding self-efficacy and breastfeeding success.
Materials and Methods: The data of the study were collected with "Descriptive Information Form, Breastfeeding Knowledge Level Diagnosis Form, LATCH Breastfeeding Diagnosis and Evaluation Scale and Postpartum Breastfeeding Self-Efficacy Scale". SPSS 25.0 (Statistical Package for Social Science) program will be used in the analysis of the data.
Design: Randomized controlled.
The study included 76 women who had normal vaginal and cesarean delivery and met the inclusion criteria (Research Research group, 38 control group) in Zeynep Kamil Gynecology and Pediatrics Education and Hospital Postpartum Postpartum Postpartum Service in Istanbul.
Study Overview
Detailed Description
Breast milk is a newborn-specific food that varies according to the baby's needs, body weight and the density that the baby can digest. Breastfeeding, on the other hand, is the most natural action that allows mother's milk to meet with the newborn. In addition to providing benefits for the growth and development of the baby, it contributes significantly to the maintenance of general health in advanced ages, the improvement of health and the reduction of the effect of risk factors affecting health. The concept of breastfeeding self-efficacy is the mother's perception of breastfeeding. Self-efficacy perception about breastfeeding determines the behavior of mothers to continue breastfeeding, whether they can cope with breastfeeding problems, their thoughts and attitudes about breastfeeding. Mother's age, education level, baby's weight and mother's number of births are concepts that can affect breastfeeding self-efficacy perception. Although there are many studies on breastfeeding in the literature, a limited number of studies have been found that determine the effect of the early results of postpartum breastfeeding education on breastfeeding self-efficacy and breastfeeding success.
This study aims to determine the effect of postpartum breastfeeding education given to women who had normal vaginal and cesarean delivery on breastfeeding self-efficacy and breastfeeding success.
The objectives of the research;
- To determine the effect of postpartum breastfeeding education given to women with normal vaginal delivery on breastfeeding self-efficacy.
- To determine the effect of postpartum breastfeeding education given to women who had cesarean section on breastfeeding self-efficacy.
- To determine the effect of postpartum breastfeeding education given to women who had normal vaginal delivery on breastfeeding success.
- To determine the effect of postpartum breastfeeding education given to women who had cesarean section on breastfeeding success.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Istanbul, Turkey
- University of Health Sciences
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
The following criteria will be taken into account for the individuals to be included in the intervention and control groups:
- Volunteering to participate in the research (Annex-1),
- Being between the ages of 18-40,
- Ability to read and write,
- Being able to read and understand Turkish,
- Not having a hearing, speaking or visual impairment,
- Having had a normal or cesarean delivery,
- Having a live birth and having a healthy baby.
Exclusion Criteria:
- Women under 18 years of age, • Women whose babies were taken to the neonatal intensive care unit.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: experiment group
Breastfeeding training will be given to each mother in the room she stays in the form of lectures and after the training, the question and answer method will be used.
In addition, the practices explained by the researcher (the way of holding the baby, grasping the breast and positioning the baby appropriately for the baby, determining the position suitable for breastfeeding and the process of expressing and storing breast milk) will be demonstrated using the mother demonstration method in order to evaluate whether the mother understands the breastfeeding education after the breastfeeding training.
Breastfeeding training will take approximately 40-45 minutes.
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Mothers in the intervention group will be given breastfeeding training after the pre-test application. The content of breastfeeding education is as follows;
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No Intervention: Control group
No attempt will be made to the mothers in the control group following the pre-test application, within the scope of the post-test application before discharge; Breastfeeding Knowledge Level Diagnostic Form, LATCH Scale and Postnatal Self-Efficacy Scale will be applied.
In addition to the breastfeeding education given to the intervention group following the post-test application to the mothers in the control group, a guide on the importance of breast milk and breastfeeding will also be given.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Introductory Information Form
Time Frame: 5 minute
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This form; mother's age, education status, social security, economic status, number of pregnancies, gestational week, type of delivery, baby's gender, desire for pregnancy, how many times she applied to a health institution during her pregnancy, which health institution she applied to for control, the status of receiving breastfeeding training during pregnancy, If she received breastfeeding training, from whom she received it, the status of reading magazines/brochures about breastfeeding during pregnancy, and the status of wanting to receive free breastfeeding training after delivery.
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5 minute
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Breastfeeding Knowledge Level Diagnosis Form
Time Frame: 10 minute
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This form, which was prepared by the researcher in order to measure breastfeeding efficiency; It consists of 15 questions about breastfeeding initiation time, breast milk storage conditions, breastfeeding positions, breastfeeding duration and frequency, general information about breastfeeding and breast milk.
Each question has three options: yes, no and I don't know. 1 point is given for each correct answer, and 0 points are given for incorrect and I don't know.
The questions in the form are mixed right and wrong.
If questions 1, 2, 3, 4, 5, 6, 9, 10, 11, 12, 14, 15 are marked as correct, and questions 7, 8, and 13 as incorrect, the highest total score that can be obtained from the form will be 15.
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10 minute
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
LATCH Scale
Time Frame: 10 minute
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This scale is a diagnostic method created in 1986 to evaluate breastfeeding success, whose scoring system is similar to the APGAR scoring system.
The application time takes about 5-8 minutes.
This diagnostic and evaluation scale has been developed to provide an objective diagnosis and evaluation of breastfeeding, to evaluate the breastfeeding success of the mother, to create a common language for health professionals and to be used in scientific studies.
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10 minute
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Postnatal Self-Efficacy Scale
Time Frame: 10 minute
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Developed by Dennis in 2003, this scale consists of 14 items.
The scale assesses how competent mothers feel about breastfeeding.
The fourteen-item scale includes a 5-point Likert-type assessment consisting of "Not at all sure: 1, Not quite sure: 2, Sometimes sure: 3, Sure: 4, Very sure: 5".
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10 minute
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- p8v6z463
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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