VIRTUAL REALITY GLASSES, CHILDREN WITH LIVER TRANSPLANTATION
NCT ID: NCT05420025
Last Updated: 2022-12-06
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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UNKNOWN
NA
15 participants
INTERVENTIONAL
2022-04-26
2023-05-27
Brief Summary
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Children with liver transplantation are in the whole treatment and care process; exposed to frequent and repetitive painful procedures. Abdominal dressings were observed to be the most frequent-repetitive, long-term source of pain affecting children physically and psychologically from these procedures. It is thought that the use of virtual reality during abdominal dressing will be beneficial because of the size of the abdominal incision and dressings, the use of no analgesic or sedative agent during dressing, and the children are affected by this incision image. It is thought that virtual reality can be used and effective in this area in terms of keeping people away from images and sounds and isolating them from real life.
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Detailed Description
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The aim of the study was to determine the effect of SGG application on pain, anxiety/anxiety, fear and physiological variables during dressing in children aged 4-10 years who had liver transplantation.
Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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CHILDREN APPLIED WITH VIRTUAL REALITY GLASSES
Before the first dressing (5 minutes before the dressing) of the children who were accepted to the Organ Transplantation A Service from the intensive care unit after the transplantation, the introductory characteristics form and scales will be applied and the physiological parameters of the child (heart rate, respiratory rate, blood pressure) will be applied by the researcher. , oxygen saturation) will be taken. Then the children will be put on SGG and the glasses will be synchronized. During the dressing, children will be shown a video with SGG, which received expert opinion beforehand. After the dressing, the physiological parameters of the children will be measured again and the scales will be applied again.
Interventions
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Eligibility Criteria
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Inclusion Criteria
* do not have a chronic or genetic disease,
* not mentally, visually or hearing impaired,
* no painful intervention is applied at least one hour before the dressing,
* no analgesic and sedative applied at least one hour before the dressing,
* both himself and his parents are open to communication and cooperation,
* Children who are first dressed in the service, who both themselves and their parents volunteer to participate in the study, and who give verbal and written consent will be included.
Exclusion Criteria
4 Years
10 Years
ALL
No
Sponsors
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Firat University
OTHER
Responsible Party
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Semiha Dertli
Research Assistant
Locations
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Firat University
Elâzığ, , Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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Emine ERDEM
Identifier Type: OTHER
Identifier Source: secondary_id
Tevfik Tolga SAHIN
Identifier Type: OTHER
Identifier Source: secondary_id
Firat Universityyyyyyyyyyy
Identifier Type: -
Identifier Source: org_study_id
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