The Effect of Virtual Reality Glasses Used During Intravenous Catheter Insertion
1 other identifier
interventional
102
1 country
1
Brief Summary
The purpose of this clinical trial is to evaluate the effect of the virtual reality glasses device on the child's emotional responses during invasive interventions in child health services. The main question it aims to answer are: \- Is there a difference between the emotional responses of children who watched cartoons with virtual reality glasses (experimental group) and the children in the control group during the intravenous catheter insertion process? First, the descriptive data form for the children was filled out for the control and study groups. Then, to distract the children during the application of the intravenous catheter, they watched cartoon videos of their choice for the 7-12 age group through virtual reality glasses by using a free internet application throughout the procedure. The procedure started with tying the tourniquet and continued until the intravenous catheter insertion was completed. During this period, the child's emotional responses were evaluated with the Children's Emotional Manifestation Scale. No intervention was applied to the control group. throughout the process the child's emotional responses were evaluated with the Children's Emotional Manifestation Scale. No intervention was applied to the control group.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2021
Shorter than P25 for not_applicable
1 active site
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
March 15, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 15, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2021
CompletedFirst Submitted
Initial submission to the registry
December 7, 2023
CompletedFirst Posted
Study publicly available on registry
January 3, 2024
CompletedJanuary 3, 2024
December 1, 2023
1 month
December 7, 2023
December 19, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The Children's Emotional Manifestation Scale (CEMS)
The scale, which allows direct behavioral observation, consists of five different behavioral categories, namely facial expression, vocalization, activity, interaction, and level of cooperation. Each category includes five different observable behaviors rated by level and intensity. The scale is scored by reviewing descriptions of the behavior in each category and selecting the value that most represents the observed behavior. Each category is scored from 1 to 5. The scores obtained for each category are summed and a total score between 5- 25 is obtained. High scale scores indicate the exhibition of more negative emotional behaviors.
7 months
Study Arms (2)
virtual reality glasses
EXPERIMENTALThe sample of the research, which was carried out as a randomized controlled experimental study, consisted of 102 children, including 51 in the control group and 51 in the study group, who were aged between 7 and 12 and were on treatment in the emergency department. Research data were collected using a Descriptive Data Form for Children and the Children's Emotional Manifestation Scale. During the data collection phase, first, the Descriptive Data Form for Children was filled out for the control and study groups. No intervention was applied to the control group. After the tourniquet was tied in the study group, the children started watching a video of their choice through virtual reality glasses. When the process was completed, the video was stopped. During this period, the child was evaluated using the Children's Emotional Manifestation Scale.
standard care
NO INTERVENTIONIntervention during intravenous catheter insertion to the child
Interventions
The population of the study consisted of children who were aged between 7- 12 and were on treatment using an intravenous catheter in the pediatric emergency unit of a state hospital in Turkey.Participants were divided into two groups, namely experimental and control groups, by using simple randomization software. The design and implementation of the study were based on the principles in the CONSORT list (Consolidated Standards of Reporting Studies). Descriptive data form for children,this form was prepared to collect information about the children included in the sample. It consists of seven questions on children's sociodemographic characteristics and previous intravenous catheter insertion experience.The Children's Emotional Manifestation Scale (CEMS), this scale was developed by Li \& Lopez (2005) to measure children's emotional responses during stressful medical procedures. The VR glasses we used in our study were connected to a mobile phone.
Eligibility Criteria
You may qualify if:
- Children who
- were aged 7-12,
- had parental permission,
- gave verbal consent,
- and whose parents could speak Turkish,
- were conscious,
- and did not have orthopedic, neurological, or sight-related problems that prevented wearing virtual reality glasses were included in the study.
You may not qualify if:
- Children who
- had a chronic disease that required frequent vascular access,
- had visual and hearing impairments,
- had a mental and neurological disability,
- had previously participated in a similar study,
- had a febrile illness at the time of application,
- had a history of fainting during vascular access procedures, or
- had used medication in the last 24 hours before the application, which might have an analgesic effect, were not included in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Türkan Şenlead
Study Sites (1)
Pamukkale University
Denizli, 20160, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Professional Nurse
Study Record Dates
First Submitted
December 7, 2023
First Posted
January 3, 2024
Study Start
March 15, 2021
Primary Completion
April 15, 2021
Study Completion
September 30, 2021
Last Updated
January 3, 2024
Record last verified: 2023-12