The Effect of Virtual Reality and Music in High-Risk Pregnants on Non-Stress Test
NCT ID: NCT05495789
Last Updated: 2023-05-12
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
102 participants
INTERVENTIONAL
2023-01-09
2023-02-10
Brief Summary
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Hypotheses H01 In the NST process, there is no difference between the NST parameters of the virtual reality group and the NST parameters of the control group.
H02 In the NST procedure, there was no difference between the anxiety score of the virtual reality group and the anxiety score of the control group.
H03 There is no difference between the satisfaction score of the group in which virtual reality was applied in the NST procedure and the satisfaction score of the control group.
H04 In the NST process, there is no difference between the NST parameters of the group to which the virtual reality is applied and the NST parameters of the musical group.
H05 In the NST procedure, there was no difference between the anxiety score of the group in which virtual reality was applied and the anxiety score of the music group.
H06 In the NST process, there is no difference between the satisfaction score of the group to which the virtual reality was applied and the satisfaction score of the music group.
H07 In NST operation, there is no difference between the NST parameters of the music group and the NST parameters of the control group.
H08 In the NST procedure, there was no difference between the anxiety score of the music group and the anxiety score of the control group.
H09 There is no difference between the satisfaction score of the music group and the satisfaction score of the control group in the NST procedure.
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Detailed Description
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Virtual Reality Group In addition to the routine procedure, virtual reality glasses will be applied to the high-risk pregnant in the virtual reality group of the research. Virtual reality glasses is a device that works on compatible smart mobile phones. After the NST device is connected and, the high-risk pregnant included in the experimental group will be made to watch a video lasting an average of 40 minutes with virtual reality glasses until the procedure is completed.
Music Group In addition to the routine procedure, the high-risk pregnant women in the music group of the research will listen to the relaxing music used in the virtual reality application with headphones.
Control Group The high-risk pregnants in the control group of the study will not be subjected to any treatment other than the routine procedure.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Virtual Reality Group
In addition to the routine procedure, virtual reality glasses will be applied to the high-risk pregnant in the virtual reality group of the research. Virtual reality glasses is a device that works on compatible smart mobile phones. After the NST device is connected and, the high-risk pregnant included in the experimental group will be made to watch a video lasting an average of 40 minutes with virtual reality glasses until the procedure is completed.
Virtual Reality
A relaxing video will be watched with virtual reality glasses.
Music Group
In addition to the routine procedure, the high-risk pregnant women in the music group of the research will listen to the relaxing music used in the virtual reality application with headphones.
Music
Relaxing music will be played by wearing headphones.
Control Group
The high-risk pregnants in the control group of the study will not be subjected to any treatment other than the routine procedure.
No interventions assigned to this group
Interventions
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Virtual Reality
A relaxing video will be watched with virtual reality glasses.
Music
Relaxing music will be played by wearing headphones.
Eligibility Criteria
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Inclusion Criteria
* Pregnant women with a single fetus
* Have eaten at least two hours before the NST procedure
* No cardiovascular disease diagnosed in the fetus,
* The participants ate at least 2 h before the NST, urinated immediately before the NST and did not smoke or drink alcohol for at least 2 h before the NST.
* Those diagnosed with high-risk pregnancy by a physician (pregnancy-induced hypertension, preeclampsia, eclampsia, gestational diabetes, premature rupture of membranes, pregnancy large or small for gestational age, intrauterine growth retardation, polihydramnios, oligohydramnios, premature birth threat, maternal age 35 age and above, maternal body mass index over 30 (obesity)
* Not having vision and hearing problems
Exclusion Criteria
* healty pregnant women
* multiple pregnancy
* having a fetus with anomaly,
* Pregnant women with fetal distress and for whom emergency intervention is considered by the physician
18 Years
FEMALE
No
Sponsors
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NESLİHAN YILMAZ SEZER
OTHER
Responsible Party
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NESLİHAN YILMAZ SEZER
Faculty of Nursing
Principal Investigators
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AYKAN YÜCEL, Prof.Dr.
Role: STUDY_CHAIR
Ankara City Hospital Bilkent
Locations
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Neslihan Yılmaz Sezer
Ankara, , Turkey (Türkiye)
Countries
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Other Identifiers
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12/125
Identifier Type: -
Identifier Source: org_study_id
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