Breastfeeding Education and Humor-Based Practices on Breastfeeding
NCT ID: NCT06299397
Last Updated: 2024-03-12
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
64 participants
INTERVENTIONAL
2023-06-14
2024-02-14
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
DOUBLE
Study Groups
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Breastfeeding-Humor group
32 pregnant women were included in the experimental group determined by randomization method. Consent to participate in the study was obtained from these pregnant women. After obtaining consent, a pre-test was conducted. Afterwards, pregnant women were given breastfeeding education and humor practice. The application was applied once a week, twice a week. An interim test was administered 1 month after the application, and a final test was administered 3 months later.
breastfeeding - humor training
Breastfeeding and humor-based practice will continue for 35-45 minutes, once a week for 2 weeks.
Control Group
After randomization, consent was obtained from the pregnant women determined that they agreed to participate in the study. The pregnant women in the control group were given a pre-test before starting the study, an interim test 1 month after the start, and a final test 3 months later.
Control Group
After randomization, consent was obtained from the pregnant women determined that they agreed to participate in the study. The pregnant women in the control group were given a pre-test before starting the study, an interim test 1 month after the start, and a final test 3 months later.
Interventions
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breastfeeding - humor training
Breastfeeding and humor-based practice will continue for 35-45 minutes, once a week for 2 weeks.
Control Group
After randomization, consent was obtained from the pregnant women determined that they agreed to participate in the study. The pregnant women in the control group were given a pre-test before starting the study, an interim test 1 month after the start, and a final test 3 months later.
Eligibility Criteria
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Inclusion Criteria
* Having a healthy pregnancy,
* Being literate,
* 32-36. Being in the gestational week,
* Being primiparous,
* Not having any psychiatric diagnosis.
Exclusion Criteria
* incompletely filling out the questionnaires
18 Years
FEMALE
Yes
Sponsors
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Inonu University
OTHER
Responsible Party
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Simge Ozturk
Principal Investigator
Principal Investigators
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Simge Ozturk, Ph.D
Role: PRINCIPAL_INVESTIGATOR
Bartın Unıversity
Locations
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Simge OZTURK
Bartın, , Turkey (Türkiye)
Countries
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Other Identifiers
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Inonu-SBF-4
Identifier Type: -
Identifier Source: org_study_id
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