The Effect of Breastfeeding Education Via Hybrid Simulation Method in the Antenatal Period on Postpartum Breastfeeding
NCT ID: NCT05624047
Last Updated: 2023-08-15
Study Results
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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COMPLETED
NA
66 participants
INTERVENTIONAL
2022-12-01
2023-08-12
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Experimental Group
Breastfeeding education using the hybrid simulation method
Breastfeeding education using hybrid simulation method
In addition to the verbal breastfeeding training given to the pregnant women assigned to the experimental group, breastfeeding training will be given using the hybrid simulation method consisting of a wearable breast model and standard patient practice.
Routine verbal breastfeeding education
Women in this group will receive oral breastfeeding training, which is routinely given in the pregnant education class and consists of one session.
Control Group
Routine verbal breastfeeding education
Routine verbal breastfeeding education
Women in this group will receive oral breastfeeding training, which is routinely given in the pregnant education class and consists of one session.
Interventions
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Breastfeeding education using hybrid simulation method
In addition to the verbal breastfeeding training given to the pregnant women assigned to the experimental group, breastfeeding training will be given using the hybrid simulation method consisting of a wearable breast model and standard patient practice.
Routine verbal breastfeeding education
Women in this group will receive oral breastfeeding training, which is routinely given in the pregnant education class and consists of one session.
Eligibility Criteria
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Inclusion Criteria
* being primipara or multipara
* being at least literate
* being planning to breastfeed
* agreeing to participate in the study
Exclusion Criteria
* preterm labor (before 37 weeks)
* either mother or baby having a health problem after birth
* being with multiple pregnancy
* being with high-risk pregnancy
18 Years
49 Years
FEMALE
Yes
Sponsors
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Bitlis Eren University
OTHER
Responsible Party
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Sultan OZKAN SAT
Assistant Professor
Principal Investigators
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Sultan Özkan Şat, Dr
Role: PRINCIPAL_INVESTIGATOR
Bitlis Eren University
Locations
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Bitlis Hüsrevpaşa Family Center
Bitlis, , Turkey (Türkiye)
Countries
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Other Identifiers
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SOZKANSAT
Identifier Type: -
Identifier Source: org_study_id
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