The Effect of Breastfeeding Support Education on Midwifery Profession Perception and Belonging

NCT ID: NCT06681753

Last Updated: 2024-11-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

74 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-11-10

Study Completion Date

2025-01-01

Brief Summary

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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

Detailed Description

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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.

Conditions

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Breastfeeding

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Pretest-posttest matched control group quasi-experimental
Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Participants
Sampling Inclusion Criteria:

* Being a senior student in the SAU Faculty of Health Sciences, Midwifery Department
* The student agrees to participate in the study

Sampling 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 Groups

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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.

Group Type EXPERIMENTAL

Experimental

Intervention Type OTHER

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.

Control

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Experimental

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.

Intervention Type OTHER

Other Intervention Names

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Control

Eligibility Criteria

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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
Minimum Eligible Age

20 Years

Maximum Eligible Age

25 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Sakarya University

OTHER

Sponsor Role lead

Responsible Party

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öznur tiryaki

associate professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Öznur Tiryaki, PhDr

Role: STUDY_CHAIR

Sakarya University

Locations

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Sakarya University

Sakarya, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Central Contacts

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Öznur Tiryaki, PhDr

Role: CONTACT

+902647271 ext. 7271

Öznur Tiryaki, PhDr

Role: CONTACT

+902647271 ext. 7271

Other Identifiers

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E-61923333-050.99-27167

Identifier Type: -

Identifier Source: org_study_id

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