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临床试验/NCT02975778
NCT02975778终止不适用

Prediction of Pain During Old People Care Measured by Skin Conductance

Hopital Foch4 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2017年6月15日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
Hopital Foch
入组人数
30
试验地点
4
主要终点
Correlation between Number of pics of skin conductance per second measured by Pain Monitor™ device with Numerical visual scale score for pain

研究概览

简要总结

The purpose of the project is to validate the use of Pain Monitor™ device, not invasive and simple of employment, for old people able to answer to a digital scale of pain intensity.

The main objective is to develop and to validate a model of prediction of the pain in old subject at the time of the care, using the measure of variation of the skin conductance.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • hospitalized patient;
  • patient over 65 years of age;
  • communicating, without cognitive impairment;
  • having to undergo an act presumed to be painful during which the patient's mobility is limited: nursing care (removal of a drain, dressing of a chronic wound, urinary catheterization, etc.), medical examination, etc.;
  • benefiting from a social security scheme or having rights;
  • having given their prior informed written consent;
  • person able to read.

排除标准

  • cutaneous anomaly on the site of measure;
  • pacemaker or internal defibrillator;
  • extremities twitching;
  • Treated by neostigmine.

结局指标

主要结局

Correlation between Number of pics of skin conductance per second measured by Pain Monitor™ device with Numerical visual scale score for pain

时间窗: 14 days

次要结局

  • Hospital Anxiety and Depression (HAD) score(14 days)
  • Percentage of efficient poses of Pain Monitor(14 days)
  • Percentage of patient refusal to use of the Pain monitor(14 days)

研究者

发起方
Hopital Foch
申办方类型
Other
责任方
Sponsor

研究点 (4)

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