- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06681753
The Effect of Breastfeeding Support Education on Midwifery Profession Perception and Belonging (Midwifery)
Associate Professor Öznur Tiryaki Sakarya University
The study was planned to provide knowledge and skills regarding breast milk and breastfeeding to midwifery students who will provide breast milk and breastfeeding consultancy to women and the society during pregnancy, birth and postpartum period after graduation, and to positively develop their professional affiliation and perception of the profession.
In this context, the following hypotheses will be tested in the study:
H0: Breastfeeding support education has no effect on the professional affiliation and perception of the profession of intern midwifery students.
H1: Breastfeeding support education increases the breastfeeding and breast milk knowledge and skills of intern midwifery students.
H2: Breastfeeding support education increases the professional affiliation of intern midwifery students.
H3: Breastfeeding support education positively develops the professional perception of intern midwifery students
Study Overview
Detailed Description
The universe of the study will consist of all students studying in the Department of Midwifery at SAU Faculty of Health Sciences, and the sample will consist of senior midwifery students. In order to determine the sample size, a power analysis will be conducted using the G*Power (v3.1.7) program. The aim of the study was to evaluate the differences in the mean knowledge level scores between the groups. The effect width value was taken as 0.70 as the method used in cases where it is not known how many units of difference are significant between the groups. The effect width value of 0.20 is very high, 0.50 is at a medium level, and 0.80 gives results under the maximum acceptance limit. As the power of the study increases, it means that the measurement is more sensitive in finding the difference. The power is expected to be 0.80 and above. In the case of a Type 1 error probability (α) of 0.05 (95% confidence interval), a power level of 80%, and an effect width value of 0.70, the study will be planned with a total of 68 students, 34 students for each group. Considering the possibility of data collection forms being incomplete and empty, 10% of the sample size (37 for each group, totaling 74 students who meet the inclusion criteria) will be included in the study. When the desired number is reached for each group during the study process, the power of the study will be calculated again (post hoc).
Criteria for Inclusion in the Sample:
- Being a senior student in the SAU Faculty of Health Sciences, Midwifery Department
- The student agrees to participate in the study
Criteria for Exclusion from the Sample:
- The student does not agree to participate in the study
- Being a 1st, 2nd and 3rd year student in the SAU Faculty of Health Sciences, Midwifery Department Data Collection Tools: Data will be collected using the Demographic Information Form containing the sociodemographic characteristics of the participants, the Breast Milk and Breastfeeding Questionnaire prepared by the researchers in line with the literature, the Midwifery Belonging Scale and the Midwifery Profession Perception Scale.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Öznur Tiryaki, PhDr
- Phone Number: 7271 +902647271
- Email: oznuritiryaki@gmail.com
Study Contact Backup
- Name: Öznur Tiryaki, PhDr
- Phone Number: 7271 +902647271
- Email: otiryaki@sakarya.edu.tr
Study Locations
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Sakarya, Turkey
- Sakarya University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being a senior student in the SAU Faculty of Health Sciences, Midwifery Department
- The student agrees to participate in the study
Exclusion Criteria:
- The student does not agree to participate in the study
- Being a 1st, 2nd or 3rd year student in the SAU Faculty of Health Sciences, Midwifery Department
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: Control
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Experimental: the Breastfeeding Consultancy and Baby Friendly Hospital Training Program
The project consultant (PT) who is a Breastfeeding Consultant and National Baby Friendly Hospital evaluator and a nurse working in the Neonatal Intensive Care Unit and who participated in the Breastfeeding Consultancy and Baby Friendly Hospital Training Program of the Ministry of Health, will provide 6 hours of theoretical and 2 hours of practical training on Breastfeeding and Breastfeeding support.
The training content will include the following topics: Breastfeeding Status in Turkey and the World, Effective Communication and Consultancy Skills, Composition of Breast Milk, Lactation and Relaxation, Breastfeeding Positions, Feeding of Babies with Special Conditions, and Benefits of Breastfeeding.
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No training will be planned for the Control Group, and their undergraduate education will be included in the study.
After the study data is collected and the study is concluded, the control group will be given breastfeeding support training from the intervention group.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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To provide intern midwifery students with breastfeeding consultancy skills.
Time Frame: 12 WEEKS
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scale scores will be evaluated
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12 WEEKS
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To ensure that they embrace the midwifery profession and gain a sense of belonging.
Time Frame: 12 WEEKS
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scale scores will be evaluated
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12 WEEKS
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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To create awareness so that they can better perceive the midwifery profession by realizing the duties, authorities and responsibilities of the profession.
Time Frame: 12 WEEKS
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scale scores will be evaluated
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12 WEEKS
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Öznur Tiryaki, PhDr, Sakarya University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- E-61923333-050.99-27167
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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