The Effect of Virtual Reality Glasses Used During Burn Dressing in Children on Parents' Satisfaction Level and Anxiety
NCT ID: NCT05373797
Last Updated: 2022-07-15
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
1 participants
OBSERVATIONAL
2021-05-07
2022-05-04
Brief Summary
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Detailed Description
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Control Group (n=26): "Parent Information Form" and "Beck Anxiety Inventory" were completed by the researcher nurse after obtaining the consent of the family and the children in the control group. After filling out the form, the parent and child were taken to the dressing room, and the researcher nurse was with both the child and the parent throughout the dressing and answered all the questions that the parent and child had. After the dressing, the child was taken to the waiting room and it was waited for the child to calm down, and "Beck Anxiety Inventory" and "Newcastle Satisfaction with Nursing Scale" were applied to the parent by the researcher nurse.
The Intervention Group (n=26): "Parent Information Form" and "Beck Anxiety Inventory" were completed by the researcher nurse after obtaining the consent of the family and the children in the intervention group. Then, the parent and child were taken to the dressing room and the child was put on virtual reality headsets and he/she watched a cartoon he/she liked. During this time, all the questions that both the child and the parent had have been answered. After the dressing, the virtual reality headsets were removed, the child was taken to the waiting room and the "Beck Anxiety Inventory" and "Newcastle Satisfaction with Nursing Scale" were applied to the parents. During all these processes, procedures were carried out in accordance with the protocols and principles established within the scope of the "COVID-19 Pandemic Measures" published by the Ministry of Health.
Conditions
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Study Design
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OTHER
OTHER
Study Groups
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experimental and control group
experimental: 26 control group:26
Procedures performed on the experimental and control groups
Intervention Group:26 Control Group (n=26):
Interventions
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Procedures performed on the experimental and control groups
Intervention Group:26 Control Group (n=26):
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* read and write,
* understand Turkish,
Exclusion Criteria
* do not want to participate in the study
* cannot be pregnant
18 Years
65 Years
ALL
Yes
Sponsors
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Ondokuz Mayıs University
OTHER
Responsible Party
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ümmühan kılıç
Principal Investigator
Principal Investigators
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Esra TURAL, PhD
Role: PRINCIPAL_INVESTIGATOR
omu
Locations
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Samsun Health Directorate
Samsun, İlkadım, Turkey (Türkiye)
19May University
Samsun, , Turkey (Türkiye)
Countries
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Other Identifiers
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health
Identifier Type: OTHER
Identifier Source: secondary_id
nineteen may university
Identifier Type: -
Identifier Source: org_study_id
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