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临床试验/NCT02765269
NCT02765269已完成不适用

Development and Testing of an Intelligent Pain Management System (IPMS) for Chinese Patients With Cancer

Xinhua Translational Institute for Cancer Pain, Shanghai1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2016年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
46
试验地点
1
主要终点
Feasibility of Mobile Application Assessed by Observing the Number of Daily Pain Assessments Recorded Among Patients

研究概览

简要总结

The purpose of this study is to determine whether the Intelligent Pain Management System (IPMS) could make recording and interfering pain timely among cancer patients with pain. The system's usability, feasibility, compliance, and satisfaction will also be assessed.

详细描述

Research indicate that over one-third of cancer patients experienced cancer pain, which is known as a major reason leading to lower quality of life of the patients.In this present study, the investigators aim to design, develop, and test the feasibility of a low cost, conveniently implemented mobile application to facilitate real-time pain recording and timely intervention among Chinese cancer patients with pain. This system evaluate real-time pain and Karnofsky Performance Status(KPS)scores for quality of life, and to generate an action plan to visit the physician or to adjust pain medication dosage when the pain threshold is reached. The investigators study is to test this system's effectiveness.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
45 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • the patient was able to read Chinese and use smart phones;
  • the patient was diagnosed with cancer and has self-reported cancer pain within a month prior to the study;
  • the patient was being seen on a regular basis by the oncology team;
  • the patient was under standard analgesia treatments;
  • the patient was estimated to have over 3 months survival time.

排除标准

  • the patients who self-reported to have severe cognitive impairments or major comorbid illnesses that would interfere with pain assessment.

结局指标

主要结局

Feasibility of Mobile Application Assessed by Observing the Number of Daily Pain Assessments Recorded Among Patients

时间窗: 2 weeks

The primary objective is to demonstrate that this mobile application is feasible by observing the numbers of daily pain assessment among patients.

次要结局

  • Karnofsky Performance Score Evaluation(2 weeks)
  • Pain Management(2 weeks)
  • Users' Satisfaction (Questionnaire)(2 weeks)

研究者

发起方
Xinhua Translational Institute for Cancer Pain, Shanghai
申办方类型
Other
责任方
Sponsor

研究点 (1)

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