The Effect of Virtual Reality Glasses Application on Labor Pain and Comfort in Multiparous Pregnants
NCT ID: NCT07013227
Last Updated: 2025-06-10
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
60 participants
INTERVENTIONAL
2023-08-01
2025-05-20
Brief Summary
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Detailed Description
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This study was planned to determine the effect of virtual reality glasses application on labor pain and comfort in multiparous pregnant women.
The research was planned at Istanbul Sultanbeyli State Hospital between 15 September 2023 and 31 June 2024. The universe of the research will be the pregnant women who were hospitalized to give birth in this hospital, and the sample will be multiparous pregnant women (60 experimental group, 60 control group) who are in the active phase of labor and comply with the sampling criteria, and a total of 120 pregnant women. Block randomization will be used in sample selection. Those who volunteered to participate in the study will have to sign the Informed Consent Form, and the Pregnant Woman Descriptive Information Form, Visual analog scale-VAS, Comfort Scale-QL and Birth Satisfaction Scale will be filled in by the researchers by face-to-face interview technique. Data collection will take approximately 15-20 minutes.As a result of the study, to reveal the effectiveness of virtual reality glasses application, which is one of the non-pharmacological methods, in reducing labor pain and increasing the birth comfort and satisfaction of mothers, and to contribute to the literature in this field by adding a new one to the limited studies in this field. This study was planned as a randomized controlled experimental study to determine the effect of virtual reality glasses application on labor pain and comfort in multiparous pregnant women.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
QUADRUPLE
Study Groups
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control group
It refers to the group in which virtual reality glasses will not be applied.
No interventions assigned to this group
experimental group
It refers to the group to which virtual reality glasses will be applied.
experimental group
Labor pain and comfort level will be measured by applying virtual reality glasses to the control group.
Interventions
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experimental group
Labor pain and comfort level will be measured by applying virtual reality glasses to the control group.
Eligibility Criteria
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Inclusion Criteria
* At least primary school graduate
* Able to speak and understand Turkish
* 37-42 weeks of pregnancy (term)
* Having a singleton pregnancy
* Fetal presentation is head
* Vaginal birth planned
* Multiparity (2 or more births)
* Does not have any risks related to pregnancy and birth
* There is no problem in the fetus
* In the active phase of labor
* Pregnant women who volunteer to participate in the study and approve the consent document will be included.
Exclusion Criteria
* Primiparity (First to give birth)
* Those who are planned to have a caesarean section
* Analgesics administered at birth
* Those who did not want to participate in the study or participated in the study voluntarily but later those who give up
18 Years
35 Years
FEMALE
Yes
Sponsors
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Marmara University
OTHER
Responsible Party
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Çiğdem
Assistant Proffesor
Principal Investigators
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zümrüt bilgin
Role: STUDY_DIRECTOR
Marmara University
Locations
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Marmara University Faculty of Health Sciences
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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MarmaraUEbelik
Identifier Type: -
Identifier Source: org_study_id
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