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The Effect of Sound-Insulated Music Playing and Fıgured Mask Nebulızer Application on the Processing Anxiety of Children

Not Applicable
Completed
Conditions
Anxiety
Child, Only
Interventions
Device: using a soundproof nebulizer with a music and a funny mask added
Device: using a silent nebulizer with no extra attachments
Device: using a routinely employed nebulizer
Registration Number
NCT05881941
Lead Sponsor
Eda SORKUN
Brief Summary

The goal of this is a randomized controlled intervention study. The study was carried out to determine the effect of nebulization treatment applied to 3-6-year-old children with a soundproof, music player and figured mask nebulizer on the child's anxiety during the procedure. The study was completed with 120 children who were admitted to the emergency room and would receive inhalation therapy. There are 3 groups in the study. These were intervention group 1 using sound-insulated music and nebulizer with figured mask, intervention group 2 using silent nebulizer, and control group using nebulizer used in routine.

Detailed Description

This is a randomized controlled intervention study. The research was carried out in Kütahya Health Sciences University Evliya Çelebi Training and Research Hospital Paediatrics Emergency Service between 1st May 2022 and 1st June 2022. The study was completed with 120 children who were admitted to the emergency room and would receive inhalation therapy. There are 3 groups in the study. These were intervention group 1 using sound-insulated music and nebulizer with figured mask, intervention group 2 using silent nebulizer, and control group using nebulizer used in routine. In order to collect data, Descriptive Information Form, State Trait Anxiety Inventory for Parents, Child Fear Scale and Child Emotional Indicators Scale were used. The data obtained in the study were evaluated with the IBM SPSS Statistics 24 (Statistical Package for Social Sciences) package program.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
120
Inclusion Criteria
  • the child should be between the ages of 3-6,
  • will receive inhaler treatment,
  • the mother or father should be with the child during the procedure,
  • not have used any sedative drugs in the last 8 hours before the application,
  • written consent has been obtained from the parents after the procedure,
  • the child is not crying before the start
Exclusion Criteria
  • the child is younger than 3 years old, older than 6 years oldu,
  • the childe has a mental disability,
  • communication with the parent havinh a problem (they cannot understand and speak Turkish, etc.),
  • the child has pain,
  • the child is the terminal period,
  • the parent has a situation that prevents the assessment of the scale (mental disability, etc.)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
using a soundproof nebulizer with a music and a funny mask addedusing a soundproof nebulizer with a music and a funny mask addedExperimental group 1: using a soundproof nebulizer with a music and a funny mask added
using a silent nebulizer with no extra attachmentsusing a silent nebulizer with no extra attachmentsExperimental group 2: using a silent nebulizer with no extra attachments
using a routinely employed nebulizerusing a routinely employed nebulizerControl group: using a routinely employed nebulizer
Primary Outcome Measures
NameTimeMethod
The Wong-Baker Faces Pain Scalepre-processing

was developed by Donna Wong and Connie Morain Baker (1981) to be used to assess children's pain levels. It was revised in 1983 for assessing pain in children over the age of three (Wong-Baker Faces Foundation-http://wongbakerfaces.org/). In this scale, the pain score is determined according to the numerical values given to the various faces (Wong \& Baker, 1988; Wong-Baker Faces Foundation-http://wongbakerfaces.org/). In our study, the researcher filled in the Wong-Baker Faces Pain Scale before the procedure in order to identify the children who were experiencing pain so that they could be excluded from the study. Only children with a pain score of "0" were taken into the study.

The Child Fear Scale (CFS)order of operation

was adapted by McMurty et al. (2011) from the Faces Anxiety Scale to measure anxiety in children undergoing painful medical procedures. The Child Fear Scale displays five faces with a range of expressions, from a neutral expression (0 = no anxiety) to a fearful face (4 = serious anxiety) (McMurtry et al., 2011). Permission is not required for the clinical and research usage of CFS. This scale was used in the study to determine the anxiety level of children before and during the procedure

The Children's Emotional Indicators Scale (CIAS)order of operation

This scale is an easy-to-evaluate and easy-to-apply scale used to objectively define the emotional indicators of children during medical procedures.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Osmangazi University

🇹🇷

Eskişehir, Centre, Turkey

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