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.
調査の概要
詳細な説明
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.
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Gülsev Kutman, Rn Msc
- 電話番号:0905521392671
- メール:glsvktmn@gmail.com
研究場所
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Tekirdağ、トルコ(Türkiye)
- 募集
- Tekirdağ City Hospital
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参加基準
適格基準
就学可能な年齢
- 子
健康ボランティアの受け入れ
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:支持療法
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的: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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実験的: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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実験的: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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介入なし: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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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Child-Reported Pain Intensity During Blood Draw Assessed Using the Wong-Baker FACES Pain Rating Scale
時間枠: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
時間枠: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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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Parent-Reported Satisfaction With the Blood Draw Procedure
時間枠: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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協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- KUTMAN-PED-2026-01
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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