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临床试验/NCT03117075
NCT03117075Unknown不适用

The Efficacy of Pain Management With Self-reporting Pain Monitoring

DERSHENG SUN3 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2017年5月15日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
68
试验地点
3
主要终点
Actual difference of pain scales

研究概览

简要总结

To compare the pain scales between clinician evaluated and reported with wearable device by patients.

详细描述

To compare the pain scales between clinician evaluated and reported with wearable device by patients with cancer of advanced stage.

研究设计

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

入排标准

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

入选标准

  • over 20 year old
  • cancer pain with visual analog scale or numeric rating scale score >/- 4
  • opioids candidates
  • with informed consent form

排除标准

  • life expectancy within 3 months

结局指标

主要结局

Actual difference of pain scales

时间窗: 1 week after using wearable pain scale device - baseline and 1 week.

comparing the pain scale assessed by wearable device and that assessed by physician when out patient clinic.

次要结局

未报告次要终点

研究者

发起方
DERSHENG SUN
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

DERSHENG SUN

clinical assistant professor

The Catholic University of Korea

研究点 (3)

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