- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06769802
The Effect of Using Nebula Bear on Anxiety and Fear During Nebulizer Application in Children
The Effect of Using Nebula Bear on Anxiety and Fear During Nebulizer Application in Children: Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Meram
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Konya, Meram, Turkey
- Necmettin Erbakan University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Are between the ages of 4-6, Parent's ability to read and write Turkish, Accompanied by their parents, Children who are willing to participate in the research will be included in the research, They receive the first nebule treatment of their hospitalization.
Exclusion Criteria:
Have mental disabilities or communication problems, Visual or hearing impairment, Those who have any body function deficiency Children who routinely use nebulizers
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Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Experimental: Nebula Bear Group
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The children in this group and their mothers will be informed about the research and their written consent will be obtained. The scale will be filled in before the application. Before the application, Nebul will introduce the teddy bear to the mother and child. The teddy bear cannot be washed because it contains an electronic device. Therefore, it will be disinfected with a solution containing 60-70% alcohol before and after use. The recorded voice will then be played to the child and mother. Then, routine nebulizer treatment will be applied and the second audio recording will be played at the end of the treatment. The researcher will be with the child. At the end of the nebulizer treatment, after the mask is removed, the Child Fear Scale and the Child Anxiety Scale-State Scale will be filled out. The Child Fear Scale will be filled in by both the mother and the nurse and the average will be taken.
Other Names:
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Active Comparator: Active Comparator: Control
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The children in this group and their parents will be informed about the research and their written consent will be obtained.
Scales will be filled in before application.
Children in this group will receive routine nebulizer treatment and routine application will be performed.
At the end of the treatment, the scales will be filled in again.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Parent and Child Information Form
Time Frame: It will be filled out by the parent within the first 60 minutes of the child's hospitalization. (Approximately 5 minute.)
|
Parent and child information form was created by researchers according to the literature.
In the form content; It contains information about introductory characteristics about the child and the family (age, mother's education level, number of children, medical diagnosis, previous hospitalization, previous use of nebule therapy) and consists of 9 questions.
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It will be filled out by the parent within the first 60 minutes of the child's hospitalization. (Approximately 5 minute.)
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Child Fear Scale
Time Frame: It will be filled out by the researcher and parent 5 minutes before the procedure and 5 minutes after the procedure (Approximately 10 minute).
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This scale was used by McMurty et al.ild or the researcher to measure children's anxiety levels.
It was developed by in 2011.
The scale was developed by Gerçeker et al. in 2018.
It has been validated in Turkish by and is aimed at children aged 4-10.
Facial muscles changes in fearful expressions were drawn by a graphic designer based on photographs of frigtened faces.
The scale can be used by the family, the child or the researcher to evaluate children.
In this scale, the child is shown a scale containing five facial expressions rated between 0 and 4 points.
While 0 indicates no fear and anxiety; 4 shows the highest fear and anxiety.
These are: "0" neutral expression (no anxiety), "1" very little fear (very little anxiety), "2" some fear (some anxiety), "3" more fear (more anxiety), "4" the most fear possible.
It is considered high fear (severe anxiety).
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It will be filled out by the researcher and parent 5 minutes before the procedure and 5 minutes after the procedure (Approximately 10 minute).
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Children's Anxiety Meter-State (CAM-S)
Time Frame: It will be filled out by the child 5 minutes before the procedure and 5 minutes after the procedure (Approximately 5 minute).
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Children's Anxiety Meter-State was developed by Ersig et al. in 2013.
A scale is a scale similar to a thermometer with horizontal lines.
It is aimed at children aged 4-10 and was developed to measure children's anxiety.
Teach kids: "Imagine all your anxious feelings are at the bottom."
When instructed" If anxious feelings are high, paint the thermometer upwards with a pencil.Before filling out the scale, the child's number ordering level should be evaluated.
Children who do not understand these instructions are not allowed to fill out the scale.
After the child makes a rating on the scale, a transparent meter is placed on the scale and the marked point is measured.Half-point increments are rounded to the nearest number.
The scale score is between 0-10.
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It will be filled out by the child 5 minutes before the procedure and 5 minutes after the procedure (Approximately 5 minute).
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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