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临床试验/NL-OMON49167
NL-OMON49167招募中不适用

The effect of Virtual Reality on post-surgical pain and recovery - VIRTUAL study

Radboud Universitair Medisch Centrum0 个研究点目标入组 100 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
12 至 99(—)

入选标准

  • 1. Patient underwent elective surgery.
  • 2. Patient reports a postoperative pain score *4 on the first postoperative day
  • at the surgical ward. Pain scores will be derived from EPIC en should also be
  • marked with *pain is not acceptable*.
  • 3. At the day of recruitment, the estimated length of stay is at least 4 days
  • after inclusion.
  • 4. Patient is willing and able to comply with the trial protocol.
  • 5. Patient is at least 16 years old on the day the informed consent form will

排除标准

  • 1. Patient suffers from delirium or acute confusional state.
  • 2. Patient has (a history of) dementia, seizure, or epilepsy.
  • 3. Patient with severe hearing/visual impairment not corrected.
  • 4. Patient is placed in isolation.
  • 5. The skin of the patient*s head or face is not intact (for example head
  • wounds, psoriasis, eczema).
  • 6. Unplanned (re)admission to the intensive care unit (ICU).
  • 7. Inclusion in another trial to evaluate new ways of treating pain

研究者

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