Breastfeeding Education Prepared With Virtual Reality Technology
NCT ID: NCT06229574
Last Updated: 2025-02-20
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
59 participants
INTERVENTIONAL
2023-11-01
2025-01-01
Brief Summary
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Detailed Description
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* Prenatal breastfeeding education prepared with virtual reality technology positively affects the breastfeeding self-efficacy of primiparous mothers.
* Prenatal breastfeeding education prepared with virtual reality technology positively affects the breastfeeding of primiparous mothers.
Participants will Pregnant women in the intervention group will be given breastfeeding training prepared with virtual reality technology and will fill out questionnaires and scales will be filled in on the first and seventh days after birth. Questionnaires will be filled in by pregnant women in the control group, and the scales will be filled out only on the first and seventh days.
Researchers will compare breastfeeding education given with virtual reality glasses with the control group to see whether it has an effect on breastfeeding success and breastfeeding self-efficacy.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
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intervention group
The effect of breastfeeding education given with virtual reality glasses on breastfeeding success and breastfeeding self-efficacy will be evaluated. The education given during pregnancy will be evaluated on the first and seventh days after birth.
virtual reality glasses
The breastfeeding software developed will be applied in this group.
control group
Breastfeeding success and breastfeeding self-efficacy of women included in this group during pregnancy will be evaluated on the first and seventh days after birth.
No interventions assigned to this group
Interventions
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virtual reality glasses
The breastfeeding software developed will be applied in this group.
Eligibility Criteria
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Inclusion Criteria
* literate,
* Pregnant women who are at 37 weeks of gestation and above,
* Those with healthy pregnancies (singleton pregnancy, no systemic/chronic disease, etc.) -Primiparous pregnant women-
* Vaginal birth planned,
* planning to breastfeed,
* Those who do not have any problems with their breasts that would make breastfeeding difficult (collapsed, missing tip, wound on the nipple, etc.),
* Pregnant women who do not have vision, hearing or communication problems
* Pregnant women who do not have any problems will be included in the study.
Exclusion Criteria
* Baby with congenital anomalies
18 Years
35 Years
FEMALE
Yes
Sponsors
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TC Erciyes University
OTHER
Responsible Party
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ipek turhan
nurse
Principal Investigators
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ipek turhan, master
Role: PRINCIPAL_INVESTIGATOR
Kayseri City Hospital
Locations
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Ipek Turhan
Kayseri, Kayseri, Turkey (Türkiye)
Countries
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Other Identifiers
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ErciyesU-SBF-IT-01
Identifier Type: -
Identifier Source: org_study_id
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