The Effect of Virtual Reality Glasses Used During Burn Dressing in Children on Parents' Satisfaction Level and Anxiety
Determination of the Effect of Virtual Reality Glasses Used During Burn Dressing in Children on Parents' Satisfaction Level and Anxiety
2 other identifiers
observational
1
1 country
2
Brief Summary
The study was planned as a prospective randomized controlled study and was carried out in the Training and Research Hospital burn unit outpatient clinic between 05.7.2021-1.04.2022. The population of the study consisted of the parents of children aged 5-10 years who applied to the burn unit polyclinic for dressing between the dates of the study. A total of 52 people were included in the research group. Data were collected by using the "Survey Form" consisting of 10 questions, "Newcastle Nursing Satisfaction Scale" and "Beck Anxiety Scale".
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started May 2021
Shorter than P25 for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 7, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 4, 2022
CompletedFirst Submitted
Initial submission to the registry
April 27, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
May 4, 2022
CompletedFirst Posted
Study publicly available on registry
May 13, 2022
CompletedJuly 15, 2022
May 1, 2022
11 months
April 27, 2022
July 13, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
The Effect of Virtual Reality Glasses Used During Burn Dressing in Children on Parents' Satisfaction Level and Anxiety
Using virtual reality glasses lowers parental anxiety
May 2022- October2022
Study Arms (1)
experimental and control group
experimental: 26 control group:26
Interventions
Intervention Group:26 Control Group (n=26):
Eligibility Criteria
In order to determine the number of samples, power analysis was performed using the G\*power program. The effect size coefficient was calculated by using the Newcastle satisfaction scale averages in source 1 (thesis), and the effect size = 0.76, and it was decided to recruit at least 26 people in each group in order to obtain 80% power at the ɑ=0.05 level, a total of 52 people in the two groups.
You may qualify if:
- parents
- read and write,
- understand Turkish,
You may not qualify if:
- under the age of 18
- do not want to participate in the study
- cannot be pregnant
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Samsun Health Directorate
Samsun, İlkadım, Turkey (Türkiye)
19May University
Samsun, 34100, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Esra TURAL, PhD
omu
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- OTHER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
April 27, 2022
First Posted
May 13, 2022
Study Start
May 7, 2021
Primary Completion
April 4, 2022
Study Completion
May 4, 2022
Last Updated
July 15, 2022
Record last verified: 2022-05