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临床试验/NCT06425835
NCT06425835尚未招募不适用

Virtual Reality in the Management of Painful or Anxiety-provoking Procedures in Emergency Departments: (Open Prospective Observational Study)

University of Monastir0 个研究点目标入组 300 人开始时间: 2024年8月15日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
300
主要终点
frequency of success

研究概览

简要总结

Study and evaluate the effectiveness of virtual reality in pain management.

详细描述

Study and evaluate the effectiveness of virtual reality in pain management.This is an open prospective observational study carried out at Urgences Fattouma Bourgiba Monastir.

For all patients included, a data collection form must be completed, mentioning age, sex, medical and surgical history, and the type of procedure planned.

  • If initial VAS >5 and intolerable: patients will immediately use painkillers and will be excluded from the study.
  • If initial VAS <=5 or > 5 but tolerable: Only VR glasses are used as an analgesic.

If during the procedure the patient describes intolerable pain: the VAS will be noted, and the patient will use a rescue analgesic (intranasal ketamine or other at the discretion of the attending physician).

The VR device consists of a pair of VR glasses with a video previously chosen and installed. Patient preparation must be done before initiating the protocol.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
9 Years 至 24 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged 09 and 24 years
  • suturing a wound
  • changing a dressing
  • lumbar puncture,
  • peripheral venous line
  • blood test
  • intramuscular injection
  • reduction of a fracture
  • casting or plastering.

排除标准

  • impaired consciousness
  • wound/infection covering the helmet area
  • intellectual/mental retardation
  • nausea, vomiting
  • patient already included in the protocol
  • pain requiring immediate medical attention. analgesic (VAS >5 and described as intolerable).

结局指标

主要结局

frequency of success

时间窗: 30 minutes

frequency of success (%) (use of emergency analgesics)

次要结局

  • reduction of pain(30 minutes)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Pr. Semir Nouira

PROFESSOR

University of Monastir

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