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临床试验/NCT07763132
NCT07763132招募中不适用

Comparison of the Efficacy of Virtual Reality and Topical Anesthetic During Venipuncture in Children: a Randomized Controlled Trial

Marie Lulková1 个研究点 分布在 1 个国家目标入组 450 人开始时间: 2024年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
450
试验地点
1
主要终点
Pain Intensity During Venipuncture

研究概览

简要总结

This randomized controlled trial evaluates methods to reduce pain during venipuncture in children aged 3 to 15 years. The study compares three approaches: virtual reality distraction using a VR headset, topical anesthesia with EMLA cream, and standard care without an additional pain-reducing intervention. The main question is whether virtual reality reduces pain during venipuncture more effectively than EMLA cream or standard care. Pain is assessed immediately after venipuncture using the Wong-Baker Faces Pain Rating Scale (0-10). The planned study sample includes 450 children.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
3 Years 至 15 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Children aged 3 to 15 years.
  • •Clinical indication for venipuncture.
  • •Written informed consent provided by a parent or legal guardian and verbal or written assent from the child, as appropriate for age and cognitive ability.

排除标准

  • •Known hypersensitivity to local anesthetics.
  • •Diagnosed mental disorder.
  • •Current treatment with analgesic or anxiolytic medications.
  • •Venipuncture not successful on the first attempt.

研究组 & 干预措施

Virtual Reality

Experimental

Children assigned to this arm receive virtual reality distraction during venipuncture using a Meta Quest 3 headset. The same 360° wildlife video is presented to all participants. Children can change the direction of view by moving their head but cannot control the content or sequence of the video. The headset is used throughout the venipuncture procedure.

干预措施: Virtual Reality Distraction (Behavioral)

EMLA Cream

Active Comparator

Children assigned to this arm receive topical EMLA cream containing lidocaine and prilocaine at the planned venipuncture site. The application site is covered with an occlusive dressing, and the cream is left in place for at least 60 minutes before venipuncture.

干预措施: Lidocaine-Prilocaine Cream (Drug)

Standard Care

No Intervention

Children assigned to this arm receive standard nursing care during venipuncture according to routine clinical practice. No additional pharmacological or non-pharmacological intervention specifically aimed at reducing procedural pain is provided.

结局指标

主要结局

Pain Intensity During Venipuncture

时间窗: Immediately after venipuncture

Pain intensity is self-reported immediately after venipuncture using the Wong-Baker Faces Pain Rating Scale (0-10), where 0 indicates no pain and 10 indicates the worst pain. Lower scores indicate lower perceived pain intensity.

次要结局

未报告次要终点

研究者

发起方
Marie Lulková
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Marie Lulková

Assistant Professor, Faculty of Health Studies

Jan Evangelista Purkyne University

研究点 (1)

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