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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05481203
Other study ID # Distraction
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2022
Est. completion date July 1, 2022

Study information

Verified date July 2022
Source Ondokuz Mayis University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aim: This research will be carried out to determine the effect of distracting methods on fear and anxiety in children before the COVID test.


Description:

Inroduction: In the literature review, it has been seen that the positive effect of different nanpharmacological methods is supported to reduce pain and anxiety caused by medical procedures. Non-pharmacological methods are classified as physical methods, cognitive behavioral methods, and environmental or emotional intervention methods. In order to draw attention to another direction, which is among these methods; watching cartoons, inflating balloons, creating balloons by blowing foam, talking about things unrelated to the initiative, virtual reality glasses, listening to music, using kaleidoscope and distraction cards etc. is located. The subject of the study is the application of distraction methods in reducing the pain associated with short-term medical interventions.


Recruitment information / eligibility

Status Completed
Enrollment 114
Est. completion date July 1, 2022
Est. primary completion date June 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 5 Years to 10 Years
Eligibility Inclusion Criteria: - children who will be taken samples for Covid 19 test - being between the ages of 5 to 10 years, - literate Exclusion Criteria: - having chronic diseasesvisual - audio, or speech impairments - mental disorders, - history of sedative, analgesic, or narcotic use within 24 h before admission - inflammatory disease during admission.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
The Kaleidescope
During the nasopharyngeal swab collection process, the researcher held a kaleidoscope to each child's eye, leisurely turning it and asking about the colors and shapes seen within it.
The visual illusion cards
Just before the nasopharyngeal swab participants were allowed to check the cards andwere askedwhat they saw in them.

Locations

Country Name City State
Turkey Ondokuz Mayis University Samsun Atakum

Sponsors (1)

Lead Sponsor Collaborator
Ondokuz Mayis University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary changing the anxiety in the Kaleidoscope group changing the anxiety scores of the children in the Kaleidoscope group during Covid 19 test up to 6 months
Primary changing the fear in the Kaleidoscope group changing the fear scores of the children in the Kaleidoscope group during Covid 19 test up to 6 months
Primary changing the anxiety in the Visual Illusion Cards group changing the anxiety scores of the children in the Visual Illusion Cards group during Covid 19 test up to 6 months
Primary changing the fear in the Visual Illusion Cards group changing thefear scores of the children in the Visual Illusion Cards group during Covid 19 test up to 6 months
Secondary changing the "Child Anxiety Scale-Stateness" score The Children's Anxiety Meter (CAM) used. It assesses children's anxiety in clinical settings and uses before medical procedures. The CAM is drawn like a thermometer with a bulb at the bottom, also includes horizontal lines at intervals going up to the top. Children are asked to mark how he/she feel "right now" to measure state anxiety. Scores range from 0 to 10. up to 6 months
Secondary changing the "Child Fear Scale" score The Child Fear Scale (CFS) used. This one-item scale consists of five sex-neutral faces. It ranges from a no fear (neutral) face on the far left to a face showing extreme fear on the far right. The rater responds indicates the level of fear. Scores range from 0 to 4. up to 6 months
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