- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07654192
The Effect of ShotBlocker and Finger Puppet on Pain and Fear During Blood Drawing in Children
The Effect of ShotBlocker and Finger Puppet on Pain and Fear During Blood Drawing in Children: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Bolu, Turkey (Türkiye)
- Abant Izzet Baysal University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being between 5 and 10 years old
- Not having chronic pain
- Not using sedative/anticonvulsant/analgesic medication
- Not having a mental or neurological disability
- Blood collection should be performed by the same nurse
Exclusion Criteria:
- Having chronic pain
- Using sedative/anticonvulsant/analgesic medication
- Having a mental or neurological disability
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Active Comparator: Shotblocker Group
Shotblocker is administered to children during the blood sampling collection process.
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Distraction techniques such as Shotblocker, which are among non-pharmacological methods, are used to reduce pain, fear, and anxiety by diverting attention away from pain and directing it toward another interesting stimulus. Once the children in the Shotblocker group sit down in the blood draw chair, the specified procedure will be applied before the blood drawing begins.
Distraction techniques such as Finger Puppet, which are among non-pharmacological methods, are used to reduce pain, fear, and anxiety by diverting attention away from pain and directing it toward another interesting stimulus.
Once the children in the Finger Puppet group sit down in the blood draw chair, the specified procedure will be applied before the blood drawing begins.
|
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Active Comparator: Finger Puppet Group
Finger Puppet is administered to children during the blood sampling collection process.
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Distraction techniques such as Shotblocker, which are among non-pharmacological methods, are used to reduce pain, fear, and anxiety by diverting attention away from pain and directing it toward another interesting stimulus. Once the children in the Shotblocker group sit down in the blood draw chair, the specified procedure will be applied before the blood drawing begins.
Distraction techniques such as Finger Puppet, which are among non-pharmacological methods, are used to reduce pain, fear, and anxiety by diverting attention away from pain and directing it toward another interesting stimulus.
Once the children in the Finger Puppet group sit down in the blood draw chair, the specified procedure will be applied before the blood drawing begins.
|
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No Intervention: Control Group
No intervention is performed on the control group during the blood sampling collection process.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Primary Outcome Measure
Time Frame: Time frame is up to 12 moths. From October 01 2025 to October 01 2026.
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The aim of this study is to evaluate the effectiveness of ShotBlocker and finger puppets in reducing pain and fear in children aged 5-10 years during blood sapmling in the pediatric blood collection unit. On the child fear scale, "0" indicates no fear; "4" indicates the highest level of fear. It consists of facial expressions ranging from 0, indicating no pain, to 10, representing severe pain. Data collection takes no more than 10 minutes. |
Time frame is up to 12 moths. From October 01 2025 to October 01 2026.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Randomization
Time Frame: Time frame is up to 15 minutes.
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Randomization in the study has been done with using a computer program (https://www.randomizer.org). To determine which children would be in the intervention and control groups, children with numbers from 1 to 90 were entered into the computer program without repetition. To avoid bias in randomisation and to increase reliability, the assignment to the intervention and control groups was made by an independent statistician. All blood collection procedures will be performed by the same nurse. A nurse with a four-year nursing diploma working in the same blood collection unit will serve as an independent observer. The observer will evaluate the children in the experimental and control groups. |
Time frame is up to 15 minutes.
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Data Collection Tools
Time Frame: Time frame is up to 15 minutes.
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In data collection, interview and observation form created by researchers (child's age, gender, previous blood sampling experience, etc.), the Children's Fear Scale, and the Wong-Baker FACES Pain Rating Scale will be used for all groups.
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Time frame is up to 15 minutes.
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Children's Fear Scale (CFS)
Time Frame: Time frame is up to 10 minutes.
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This scale is rating from 0 to 4 with five drawn facial expressions representing a range from a neutral expression (0 = no fear) to a frightened face (4 = extreme fear).
It may be used by parents and researchers before and during the procedure for children.
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Time frame is up to 10 minutes.
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Wong-Baker FACES (WB-FACES) Pain Rating Scale
Time Frame: Time frame is up to 10 minutes.
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This scale is used to rate pain in children aged 3 years and older.
The scale consists of facial expressions ranging from 0, indicating no pain, to 10, representing severe pain.
Children are asked to select the facial expression that most accurately reflects the intensity of their pain, and then a score is assigned.
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Time frame is up to 10 minutes.
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ShotBlocker
Time Frame: Time frame is up to 5 minutes.
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ShotBlocker was used on children in the ShotBlocker group during blood sampling.
ShotBlocker device (Bionix LLC, Maumee, Ohio, USA) is a drug-free, flexible, and U-shaped, non-invasive plastic apparatus with small protrusions.
It is placed directly on the skin and has a slit in the middle for inserting the needle.
It is pressed firmly onto the skin, and the blunt contact points provide painless physical stimulation.
This blocks the perception of pain caused by needle insertion, which is consistent with the "gate control" theory of pain.
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Time frame is up to 5 minutes.
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Finger Puppet
Time Frame: Time frame is up to 5 minutes.
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Finger puppets were used on children in the finger puppet group during blood sampling.
Finger puppets consist of plush toys featuring various animal figures that can be worn on adults' fingers.
The researcher put on the finger puppet chosen by the child and spoke to the child by imitating animal sounds.
After the intervention, finger puppets were given as gifts to the children who wanted them.
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Time frame is up to 5 minutes.
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Data Collection
Time Frame: Time frame is up to 15 minutes.
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The same nurse will perform the blood collection procedure on the children.
A nurse with a four-year nursing degree working in the same blood collection unit will become an independent observer.
The observer will assess the pain and fears of the children in the experimental and control groups using scales.
The researcher will give the interview and observation form to the parent to fill out before the blood drawing.
The child's level of fear regarding the procedure will be recorded using the CFS by asking separate questions to the child, parent, and observer before the procedure.
The child's fear of the procedure and pain will be separately assessed and recorded by the child, parent, and observer after the procedure.
The child, parent, and observer independently and simultaneously evaluated the scales will be used.
The ShotBlocker and finger puppet will be administered to the children in the experimental groups by the same researcher.
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Time frame is up to 15 minutes.
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Collaborators and Investigators
Sponsor
Publications and helpful links
Helpful Links
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- AIBU-SBF-CC-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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