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Effect of Virtual Reality Headsets on Fear Anxiety and Physiological Parameter in Skin Prick Test

Effect of Virtual Reality Headsets on Pain, Anxiety, Fear and Physiological Parameters in Children Who Had Skin Prick Test Applied

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06401408
Enrollment
32
Registered
2024-05-06
Start date
2024-06-20
Completion date
2025-04-01
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Allergy

Keywords

allergy

Brief summary

The goal of this clinical trial is determine the effect of virtual reality headsets on pain, anxiety, fear and physiological parameters in children aged 4-7 years who undergoing skin prick test. The main questions it amis to answer are: Virtual reality headsets effect on the pain that during the procedure Virtual reality headsets effect on the anxiety that occurs during the procedure Virtual reality headsets effect on the fear that occurs during the procedure Virtual reality headsets effect on physiological parameters (heart rate, blood pressure, respiratory rate) during the procedure

Detailed description

Before starting the skin prick test, the child and his/her family who meet the inclusion criteria of the study will be informed about the use of virtual reality headsets(VRH) and volunteer consent forms will be obtained. Before starting the test (5 minutes before), the Introductory Characteristics Form for Children and Their Families and scales (so that the pain, fear and anxiety scores predicted by the children before the procedure will be measured) will be applied to the children and the child's physiological parameters (heart rate, blood pressure, respiratory rate, oxygen saturation value) will be taken. Then, the children will be fitted with an VRH and watched an animated film (approximately 15 minutes long) determined in line with the child's age group, developmental characteristics and expert opinions.After the child starts watching the video, skin prick test procedures will be initiated and the child will be allowed to watch the video until the test ends. After the test is completed (5 minutes later), physiological parameters will be taken again and scales (thus measuring the pain, fear and anxiety scores felt by the children during the procedure) will be applied. Control group application phase: No intervention/application will be performed on the children who will be included in the control group. The Introductory Characteristics of Children and Their Families Form and scales will be administered to the children in the control group simultaneously with the experimental group (in the form of pretest-posttest). Additionally, physiological parameters will be taken simultaneously with the experimental group.

Interventions

None listed

Sponsors

TC Erciyes University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
4 Years to 7 Years
Healthy volunteers
Yes

Inclusion criteria

1. Between the ages of 4-7, 2. Does not have a chronic or genetic disease, 3. No mental, visual or hearing impairment, 4. No analgesics or sedatives were administered at least one hour before the test procedure, 5. Both he and his parents are open to communication and cooperation, 6. Children who both themselves and their parents volunteer to participate in the research and give verbal and written consent will be included.

Exclusion criteria

1. Those who are outside the 4-7 age range, 2. Having a chronic or genetic disease, 3. Mentally, visually or hearing impaired, 4. Applying analgesics and sedatives at least one hour before the test procedure, 5. The child who cannot adapt to virtual reality glasses, 6. Both he and his parents do not cooperate, 7. Children who neither they nor their parents volunteer to participate in the research and who do not give verbal or written consent will not be included in the research.

Design outcomes

Primary

MeasureTime frameDescription
Children's Fear Scale (CFS)4 weeksTo conduct an initial investigation of the psychometric properties of the Children's Fear Scale (CFS; based on the adult Faces Anxiety Scale) with young school-age children.The Child Fear Scale (CFS) developed by McMurtry et al. is used to assess the fear levels of children aged 4-10 years. In the scale, 5 cartoon face pictures are used. Anxiety level is evaluated with numbers between 0 and 4. A score of 0 indicates no anxiety and a score of 4 indicates severe anxiety. The validity and reliability of the scale was conducted by Ozalp-Gerceker et al. in 2018. The content validity index is 0.89.Support was found for interrater reliability and test retest reliability of the CFS for measuring children's fear during venipuncture.

Secondary

MeasureTime frameDescription
Children's Anxiety Meter-State (CAM-S)4 weeksThe CAM scale is drawn to resemble a thermometer with a bulb at the bottom and horizontal lines at intervals going up to the top. Children are instructed to Pretend that all of your worried or nervous feelings are in the bulb or bottom part of the thermometer. If you are a little bit worried or nervous, the feelings might come up in the thermometer just a little bit.Put a line on the thermometer showing how much worry or nervousness you feel.When children did not understand this analogy, we used an alternate script that did not explicitly describe a thermometer. Children were asked to Pretend that all of your worried or nervous feelings are in the very bottom down here. If you are a little bit worried or nervous, the feelings might come up just a little bit. If you are very, very worried or nervous, the feelings might go all the way to the top. Put a line showing how much worry or nervousness you feel.

Countries

Turkey (Türkiye)

Contacts

Primary ContactKazim Bagci
kazimbagci@erciyes.edu.tr+905336573633
Backup ContactEmine Erdem, Prof. Dr.
emine@erciyes.edu.tr+905326066277

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026