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临床试验/ChiCTR1800016589
ChiCTR1800016589尚未招募1 期

Effects of immersive virtual reality intervention on pain and anxiety among paediatric cancer patients undergoing peripheral intravenous cannulation: A randomized controlled trial

未提供1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2018年8月1日最近更新:

试验速览

阶段
1 期
状态
尚未招募
入组人数
200
试验地点
1
主要终点
疼痛

研究概览

简要总结

This study aims to examine the effects of IVR intervention on reducing pain, anxiety, stress, and length of procedure among pediatric patients undergoing venipuncture. The satisfaction ratings of health care providers toward the procedures and the cost effectiveness of the IVR intervention will also be evaluated.

研究设计

研究类型
Interventional
主要目的
随机平行对照
盲法
Given the nature of the intervention, blinding of participants, RN, and health care provider will be difficult.

入排标准

年龄范围
4 至 17(—)
性别
All

入选标准

  • Pediatric patients: (1) aged between 4 and 17 years; (2) scheduled to undergo venipuncture; and (3) can understand Chinese and follow instructions.

排除标准

  • Potential participants will be excluded according to the following: (1) identified cognitive and learning problems in their medical record; (2) sensory impairment to pain (such as spinal bifida); (3) identified contact precautions; and (4) previous history of seizures or motion sickness.

研究组 & 干预措施

Experimental group

Immersive virtual reality

Control group

receive standard care only

结局指标

主要结局

疼痛

次要结局

  • 焦慮
  • 緊張
  • 干預時長

研究者

发起方
未提供

研究点 (1)

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