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临床试验/NCT04804735
NCT04804735已完成不适用

Use of Virtual Reality Mask or Music Therapy for Analgesia and Anxiolytic Purpose When Totally Implanted Venous Access Device (IVAD) for Chemotherapy Under Local Anesthesia

Institut Curie5 个研究点 分布在 1 个国家目标入组 127 人开始时间: 2022年12月6日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
127
试验地点
5
主要终点
mean of pain felt during the whole IVAD procedure

研究概览

简要总结

Evaluate 2 medical devices on pain average and/or anxiety average in the totally Implanted Venous Access Device (IVAD) procedure under local anesthesia.

详细描述

Evaluate the efficacy of virtual reality and music therapy on pain average and/or anxiety average in the totally Implanted Venous Access Device (IVAD) procedure under local anesthesia.

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
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient aged between 18 and 85 years.
  • Patient with cancer care and having a totally Implanted Venous Access Device (IVAD) procedure under local anesthesia for chemotherapy.
  • Absence of anxiolytic premedication.
  • Patient affiliated to social insurance.
  • Absence of contra-indication to the use of virtual reality, music therapy instrument or local lidocaine anesthesia.
  • Signed informed consent form.

排除标准

  • Patient already participated to this study.
  • Patient deprived of liberty or under legal representative or under curatorship.
  • Psychiatric disease enabling communication.
  • Deafness or visual impairement.
  • Patient under beta-blockers medication.
  • Chronic pain present and not equilibrated before the measured procedure as > 3 by the NRS.
  • Tracheotomy.
  • Low cervical tumor, or bilateral low cervical adenopathies.
  • Compression or jugular stenosis (uni or bilateral).
  • Jugular or subclavian thrombosis.
  • Patient under anticoagulants medication or having hesmostasis troubles.
  • Claustrophobia or thalassophobia inducing the possibility of rejecting the virtual reality mask or music therapy mask.
  • Patients not speaking french.
  • Pregnant and breastfeeding women.

结局指标

主要结局

mean of pain felt during the whole IVAD procedure

时间窗: 1 day

pain means will be measured with the Numerical Rating Scale (NRS) from 0 to 10 with 0 corresponding to no pain and 10 the maximum pain feeling.

mean of anxiety felt during the whole IVAD procedure

时间窗: 1 day

Anxiety means will be measured with the Numerical Rating Scale (NRS) from 0 to 10 with 0 corresponding to no anxiety and 10 the maximum anxiety feeling.

次要结局

  • Global patient satisfaction of NRS and comparison between the 3 groups.(1 day)
  • Pain NRS means felt during the procedure and comparison.(1 day)
  • Correlation coefficient between the ANI air under the curve and the pain measure with the numerical rating scale.(1 day)
  • Tolerance evaluated by NRS and responses to the closed questions (dizziness, nausea, suffocating feeling) completed at the end of the procedure.(1 day)
  • Anxiety NRS means felt during the procedure and comparison.(1 day)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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