Atraumatic Care Practice From the Child and Parent Perspective
NCT ID: NCT06172972
Last Updated: 2023-12-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
219 participants
INTERVENTIONAL
2023-03-01
2023-06-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Atraumatic nursing care group
Before the phlebotomy, children in the intervention group were allowed to choose a distracting method (foam balloons, stress balls, musical books) to be occupied with during the procedure. It was ensured that the parent was staying with the child and that the child played with this material during the procedure (making a foam balloon, squeezing the ball with the hand in which the procedure was not carried out and reading the book with the parent
Atraumatic nursing care
Children in the intervention group were allowed to choose a distracting method (foam balloons, stress balls, musical books) to be occupied with during the procedure
Control group
The parents of the children in the control group were ensured to stay with their children during the procedure, and the child's attention was distracted by the nurse asking questions about the child's name, age, and what grade the child was in. This is one of the methods frequently used in Turkiye.
No interventions assigned to this group
Interventions
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Atraumatic nursing care
Children in the intervention group were allowed to choose a distracting method (foam balloons, stress balls, musical books) to be occupied with during the procedure
Eligibility Criteria
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Inclusion Criteria
* being between 5-10 years of age
* having no visual, intellectual or neurological disabilities
* having the phlebotomy procedure carried out with a single attempt
* not having a disease that causes chronic pain
* being accompanied by either mother or father during the procedure
* not taking painkillers or sedating drugs before the phlebotomy procedure
Exclusion Criteria
* having visual, audio, or speech impairments
* having a disease that causes chronic pain
* with a history of sedative and analgesic use within 24 h prior to admission
* filling out the data collection forms incompletely
5 Years
10 Years
ALL
Yes
Sponsors
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Ondokuz Mayıs University
OTHER
Responsible Party
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Hatice Uzşen
Principal Investigator
Principal Investigators
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Esra Tural Büyük, PhD
Role: STUDY_CHAIR
Ondokuz Mayıs University
Locations
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Hatice Uzşen
Samsun, Atakum, Turkey (Türkiye)
Countries
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Other Identifiers
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Atraumatic Care
Identifier Type: -
Identifier Source: org_study_id