- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06810102
Vırtual Realıty Glasses' Traumatıc Bırth Perceptıon and Bırth Preferences
The Effect of the Bırth Process Watched to Nursıng Students Through Vırtual Realıty Glasses on the Students' Perceptıon of Traumatıc Bırth and Bırth Preferences
Birth is an irreplaceable experience in an individual's life, and can have critical health consequences for both the mother and the baby. Healthcare professionals, especially nurses, play an important role in the management, support and education of this process. Nursing students' knowledge and experience about labor is an important factor that affects both their professional development and future patient care.
Traditional education methods may have limited impact on healthcare professionals in learning about the birth process. Instead, the use of virtual reality (VR) technology offers students the opportunity to experience the birth process realistically. In a virtual reality environment, nursing students can understand the physiological stages of birth, its effects on the mother and baby, and the emotional aspects of the birth process more deeply. This has the potential to change traumatic perceptions of the birth process, and can also have an impact on birth preferences.
The perception of traumatic birth is shaped by individuals' negative thoughts and feelings about their birth experiences. These perceptions emerge as an important factor affecting future birth preferences and health care application status beyond the birth process. During nursing education, shaping these perceptions of students and providing them with positive experiences is of critical importance. Experiencing labor with virtual reality can reduce students' negative perceptions of birth and help them make more conscious choices about birth options.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Elazığ, Turkey, 23100
- NURDİLAN
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being a woman
- Having taken a gynecology course
Exclusion Criteria:
- Having witnessed any labor before,
- Having any psychiatric diagnosis,
- Having any neurological disease (such as epilepsy) that will cause seizures,
- Having any diagnosis that causes dizziness in the patient, such as vertigo.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: experimental
Before the lesson, students will watch a video of the actual birth.
The video is available on YouTube (https://www.youtube.com/watch?v=IRjOO6V83Uw) and was edited and voiced by the researcher to its final form.
The video includes observations starting before birth, the birth itself and the early postpartum period.
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There will be a video screening
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No Intervention: control
No intervention will be made
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
traumatic perception of birth
Time Frame: 1 month
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It is thought that showing the birth process to nursing students through virtual reality will reduce the score they will receive on the traumatic birth perception scale and reduce the perception of traumatic birth.
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1 month
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Birth preferences
Time Frame: 1 month
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It is thought that by showing the birth process to nursing students in virtual reality, birth preferences will change and the rate of cesarean births will decrease.
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1 month
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- fıratuniversty
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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