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CompletedNCT06541964Updated Nov 15, 2024

Two Different Distraction Methods for Reducing Procedural Pain in Children

An interventional study of Parent-Provide Distraction and Windmill Toy Blowing in Procedural Pain, sponsored by Maltepe University. Completed at 1 site in Turkey. Open to participants aged 6 Years to 12 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-11-15.

Sponsored by Maltepe University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
66
Allocation
Randomized
Ages
6 Years to 12 Years
Sex
All
01

Study summary

This research will be carried out in a randomized controlled experimental design in order to study the effect of parent-provide distraction and windmill toy blowing methods in reducing the pain caused by blood collection in children aged 6-12 who have applied to the children's blood collection unit. It will be taken by randomization so that there is no bias in the people who will be included in the study. Randomization table "https://www.calculatorsoup.com " it was created using.

After randomization, the children in the parent-provide distraction group with parental participation will be asked riddles by the parent during the venous blood collection procedure. The children in the windmill toy blowing group will blow a windmill toy during the venous blood collection process. For the children in the control group, no distraction will be made during venous blood collection. As soon as the procedure is completed, the pain score during the procedure and the pain score will be evaluated one minute after the procedure. The evaluation will be made by the child, parent and nurse who draws blood.

Read the detailed description

Many different non-pharmacological methods are used to cope with adverse conditions such as pain caused by invasive procedures in children. One of these non-pharmacological methods is distraction. The American Pain Association recommends the use of distractions for pain control in children. By focusing the child's attention in another direction, the child's pain is controlled and reduced. As distraction methods, video games, virtual reality glasses, listening to music, watching cartoons, blowing balloons, reading books, blowing windmill toys, parent-provide distraction are used.

The aim of this study is to determine the effects of parent-provide distraction and windmill toy blowing in reducing pain during blood collection in children aged 6-12 years. Power analysis was performed to determine the number of people to be included in the research. The strength of the test was calculated using the G*Power 3.1 program. As a similar research in the relevant literature, the effect size of the difference in pain was calculated as 1.557 in the research conducted by Orhan (2020). In order to exceed the 95% value in determining the strength of the study, 51 people, including 17 people in groups with a significance level of 5% and an effect size of 1,557, must be reached (df=32; t=2,036). In the research, it was aimed to reach a total of 66 people, including 22 people in groups, taking into account the high strength of the test and the losses.

The Information Form, Wong Baker Faces Scale, VAS will be used for data collection. First of all, those who meet the criteria for inclusion in the research and research the purpose of the research will explain to the parents who volunteered to participate and their children by explaining the purpose of the research information about the research will be provided by the executor. Then about their participation in the study written and oral consent will be obtained from parents, and oral consent will be obtained from children. By obtaining information from the parent the information form will be filled out by the researcher before the blood collection procedure. Blood collection procedure it will be performed by a single experienced nurse Parental participation in the group of diverting attention information about the riddles will be provided by the researcher. By the research manager parents and children will be given information about the Wong Baker Faces Scale. Research manager children in the windmill toy blowing group will be supervised by blowing the windmill. No intervention will perform to reduce pain in the control group. In all groups, as soon as the procedure is completed and 1 minute after the procedure, the child's pain will be evaluated with the Wong Baker Faces Scale. The nurse and the parent will evaluate the child's pain with VAS. During the evaluation, pain assessments will be made in such a way that the child, parent and nurse will not see each other in order not to be affected by each other. It is estimated that the data collection process will take about 10-15 minutes.

02

Conditions studied

  • Procedural Pain

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Keywords

  • Pain
  • Venous Blood Collection
  • Distraction
03

In context

Pain, Procedural

237 studies on the registry are indexed under Pain, Procedural; 64 are open to participants now.

This study's enrollment of 66 is below the median of 83 across 223 interventional studies indexed under Pain, Procedural.

Browse Pain, Procedural studies →

Lead sponsor

Maltepe University is the lead sponsor of 62 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years to 12 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • The children whose between 6 and 12 years old,
  • The children does not have a visual, hearing or mental problem,
  • The children and the parent's knowledge of Turkish at the level of the mother tongue,
  • The voluntary consent of the children and his/her parent to participate in the research.

Exclusion criteria

Exclusion Criteria:

  • The children whose younger than 6 years and older than 12 years,
  • The children have a visual, hearing or mental problem,
  • The children and the parent's inability to speak Turkish at the level of their native language,
  • The children and the parent do not agree to participate in the research.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
66 participants (actual)

Study arms

  • Experimental
    Parent-Provide Distraction Group

    Parent-Provide Distraction Group

    Other: Parent-Provide Distraction

  • Experimental
    Windmill Toy Blowing Group

    Windmill Toy Blowing Group

    Other: Windmill Toy Blowing

  • Other
    Control Group

    Control Group

    Other: Control

Interventions

  • OtherParent-Provide Distraction

    The children will be asked riddles by their parents for 5 seconds before and during the blood collection procedure.

  • OtherWindmill Toy Blowing

    The children will blow on the windmill toy for 5 seconds before and during the blood collection procedure.

  • OtherControl

    No intervention will make on the children.

06

What researchers measure

Primary outcomes

  1. Pain Evaluated by Children (Wong-Baker Faces Scale)

    Pain will be assessed by children with Wong-Baker Faces Scale. It is a valid and safe individual notification-based scale used to describe pain in children aged 3-18 (Wong-Baker Faces Foundation-http://wongbakerfaces.org/). It consists of 6 facial expressions ranging from smiling face to crying facial expression, which are scored Dec Decently from 0 to 10 to describe the severity of pain. As the score obtained from the scale increases, the severity of pain increases, and the severity decreases as the score decreases. "Face 0" means that there is no pain. He has a smiley face expression. "Face 2" has a little pain. "Face 4 " has a little more pain. There are more than "face 6" pain. The "face 8" pain is quite a lot. The pain of "face 10" is unbearable. The severity of the pain can be defined by enabling children to choose the shape of the face from the expression of their pain.

    Time frame: During venipuncture procedure (when needle insertion and the first blood was seen in injector, until needle removed), and one minute after venipuncture procedure (one minute after the injector was removed)

Secondary outcomes

  1. Pain Evaluated by Parents and Nurse (Visual Analog Scale)

    Pain will be assessed by parents and nurse with Visual Analog Scale. The scale developed by Freyd was used to determine the severity of pain. VAS is the scaled version of a 10-centimeter line from 1 to 10. a value of 10 indicates maximum pain, while a value of 0 means that there is no pain at all. He is asked to mark the appropriate place on the scale according to the level of pain. The pain score is determined by measuring with a ruler. This scale is a safe and widely used measurement tool accepted in the literature.

    Time frame: During venipuncture procedure (when needle insertion and the first blood was seen in injector, until needle removed), and one minute after venipuncture procedure (one minute after the injector was removed)

07

Study locations

1 site
  • Maltepe University
    Istanbul, Turkey
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 15, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06541964
Lead sponsor
Maltepe University
Responsible party
Zeynep Erkut (Assistant Professor, PhD, Maltepe University) — Principal investigator
First posted
Aug 7, 2024
Start date
Aug 30, 2024
Primary completion
Nov 13, 2024
Completion
Nov 13, 2024
Last update
Nov 15, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Nov 2024. You cannot join it, but the record below documents what was studied.

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