Distraction Methods for Reducing Pain and Fear During Blood Draw in Children (PED-DISTRACT)
Effects of Pinwheel Blowing, 3D Hologram Viewing, and Gum Chewing on Pain and Fear During Blood Draw in Children: A Randomized Controlled Trial
Blood draw is a common invasive procedure that can cause pain and fear in children. This randomized controlled trial aims to compare the effects of pinwheel blowing, 3D hologram viewing, and sugar-free gum chewing on pain and fear during blood draw among children aged 5-10 years. Parental satisfaction with the care provided during the procedure will also be evaluated.
A total of 164 children will be assigned in a 1:1:1:1 ratio to the pinwheel blowing, 3D hologram viewing, gum chewing, or control group using block randomization stratified by age and sex. The interventions will begin one minute before the blood draw and continue until the procedure is completed. Children in the control group will receive the routine blood draw procedure without any additional nonpharmacological intervention.
Immediately after the blood draw, the child's pain and fear during the procedure will be independently evaluated by the child, the accompanying parent, and an independent observer nurse. Parental satisfaction will also be assessed after the procedure.
研究概览
详细说明
This study is a four-arm, parallel-group randomized controlled trial involving children aged 5-10 years undergoing blood draw in a pediatric phlebotomy unit. The study aims to compare three nonpharmacological methods involving different mechanisms: active distraction through pinwheel blowing, passive visual distraction through 3D hologram viewing, and rhythmic oral and gustatory stimulation through flavored gum chewing.
Eligible children will be assigned to the study groups in a 1:1:1:1 ratio using block randomization stratified by sex (female or male) and age group (5-7 or 8-10 years). A block size of four will be used within each stratum.
In the pinwheel blowing group, children will begin blowing a colorful handheld pinwheel one minute before the blood draw and continue until the procedure is completed. In the 3D hologram viewing group, children will watch an age-appropriate holographic video featuring colorful flying butterflies, beginning one minute before the blood draw and continuing until the procedure is completed. In the gum chewing group, children will select a flavored sugar-free gum, begin chewing it one minute before the blood draw, and continue throughout the procedure. Children in the control group will receive the routine blood draw procedure without any additional pharmacological or nonpharmacological pain-relieving intervention. The accompanying parent will remain with the child throughout the procedure.
All blood draws will be performed by the same nurse, who has at least five years of pediatric phlebotomy experience, using a standardized procedure. Pain experienced during the blood draw will be assessed using the Wong-Baker FACES Pain Rating Scale, which ranges from 0 to 10. Fear will be assessed using the Children's Fear Scale, which ranges from 0 to 4. Immediately after the procedure, pain and fear will be rated independently by the child, the accompanying parent, and an independent observer nurse. Parental satisfaction will be evaluated using a single-item numerical rating scale ranging from 1 to 10.
Because of the visible nature of the interventions, the children, parents, researcher delivering the interventions, phlebotomy nurse, and observer nurse cannot be blinded to group allocation.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Gülsev Kutman, Rn Msc
- 电话号码:0905521392671
- 邮箱:glsvktmn@gmail.com
学习地点
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Tekirdağ、土耳其(türkiye)
- 招聘中
- Tekirdağ City Hospital
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参与标准
资格标准
适合学习的年龄
- 孩子
接受健康志愿者
描述
Inclusion Criteria:
- Children aged 5 to 10 years
- Scheduled to undergo a blood draw
- No analgesic medication use within 6 hours before the procedure
- No visual, hearing, or speech impairment
- No neurological disorder
- No oral or jaw condition that may prevent gum chewing
- No chronic illness requiring frequent invasive procedures
- Written informed consent provided by the parent or legal guardian
- Verbal assent provided by the children
Exclusion Criteria:
- Previous history of syncope during blood draw procedures
- Blood draw not completed on the first attempt
- Development of syncope during the procedure
- Inability or unwillingness to complete the assigned intervention
- Withdrawal of consent or assent by the parent or child at any stage of the study
学习计划
研究是如何设计的?
设计细节
- 主要用途:支持治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:3D Hologram Viewing Group
Children will watch an age-appropriate 3D holographic video featuring colorful flying butterflies.
The intervention will begin one minute before the blood draw and continue until the procedure is completed.
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Children will watch an age-appropriate 3D holographic video featuring colorful flying butterflies.
The holographic display will be positioned approximately 50 cm from the child.
The intervention will begin one minute before the blood draw and continue until the procedure is completed.
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实验性的:Pinwheel Blowing Group
Children will begin blowing a colorful handheld pinwheel one minute before the blood draw and continue until the procedure is completed.
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Children blow a colorful handheld pinwheel with a diameter of 16 cm.
The intervention begins one minute before the blood draw and continues until the procedure is completed.
Children hold the pinwheel with the hand not used for blood collection; the researcher holds it when necessary.
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实验性的:Gum Chewing Group
Children will select a flavored sugar-free gum, begin chewing it one minute before the blood draw, and continue until the procedure is completed.
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Children will select a 14.5-g piece of sugar-free flavored gum and begin chewing it one minute before the blood draw.
The available flavors will include watermelon, strawberry, orange, and mixed fruit.
Children will continue chewing the gum until the procedure is completed.
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无干预:Control Group
Children will receive the routine blood draw procedure used in the pediatric phlebotomy unit.
No additional pharmacological or nonpharmacological pain-relieving intervention will be provided.
The accompanying parent will remain with the child and may talk to and maintain eye contact with the child during the procedure.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Child-Reported Pain Intensity During Blood Draw Assessed Using the Wong-Baker FACES Pain Rating Scale
大体时间:Immediately after the blood draw, within approximately 5 minutes
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Pain experienced during the blood draw will be assessed by the child using the Wong-Baker FACES Pain Rating Scale.
The scale consists of six faces scored as 0, 2, 4, 6, 8, and 10, where 0 indicates no pain and 10 indicates the worst possible pain.
Higher scores indicate greater pain intensity.
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Immediately after the blood draw, within approximately 5 minutes
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Child-Reported Fear During Blood Draw Assessed Using the Children's Fear Scale
大体时间:Immediately after the blood draw, within approximately 5 minutes
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Fear experienced during the blood draw will be assessed by the child using the Children's Fear Scale.
The scale consists of five facial expressions scored from 0 to 4, where 0 indicates no fear and 4 indicates extreme fear.
Higher scores indicate greater fear.
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Immediately after the blood draw, within approximately 5 minutes
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Parent-Reported Satisfaction With the Blood Draw Procedure
大体时间:Immediately after the blood draw, within approximately 5 minutes
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Parental satisfaction with the care provided during the blood draw procedure will be assessed using a single-item numerical rating scale ranging from 1 to 10, where 1 indicates the lowest level of satisfaction and 10 indicates the highest level of satisfaction.
Higher scores indicate greater parental satisfaction.
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Immediately after the blood draw, within approximately 5 minutes
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
关键字
其他相关的 MeSH 术语
其他研究编号
- KUTMAN-PED-2026-01
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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