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.
연구 개요
상태
상태
정황
정황
개입 / 치료
개입 / 치료
상세 설명
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.
연구 유형
연구 유형
등록 (추정된)
등록
단계
단계
- 해당 없음
연락처 및 위치
연구 연락처
연구 연락처
- 이름: Gülsev Kutman, Rn Msc
- 전화번호: 0905521392671
- 이메일: glsvktmn@gmail.com
연구 장소
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-
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Tekirdağ, 터키 (Türkiye)
- 모병
- Tekirdağ City Hospital
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참여기준
자격 기준
자격 기준
공부할 수 있는 나이
- 어린이
건강한 자원 봉사자를 받아들입니다
설명
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
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 지지 요법
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
팔의 수
무기와 개입
참가자 그룹 / 팔참가자 그룹 / 팔 |
개입 / 치료개입 / 치료 |
|---|---|
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실험적: 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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실험적: 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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실험적: 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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간섭 없음: 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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연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Child-Reported Pain Intensity During Blood Draw Assessed Using the Wong-Baker FACES Pain Rating Scale
기간: 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
기간: 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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2차 결과 측정
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Parent-Reported Satisfaction With the Blood Draw Procedure
기간: 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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공동 작업자 및 조사자
협력자
협력자
수사관
수사관
- 수석 연구원: Gülsev Kutman, Tekirdağ City Hospital
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
연구 시작
기본 완료 (추정된)
기본 완료
연구 완료 (추정된)
연구 완료
연구 등록 날짜
최초 제출
최초 제출
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
처음 게시됨
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
마지막 업데이트 게시됨
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
키워드
추가 관련 MeSH 약관
기타 연구 ID 번호
기타 연구 ID 번호
- KUTMAN-PED-2026-01
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
IPD 계획 설명
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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