跳至主要内容
临床试验/NCT05628246
NCT05628246已完成不适用

Telemedicine Versus In-Person Follow-up for Cancer Pain Management: An Equity and Cost Analysis Comparison Using a Prospective Quasi-Experimental Design

Mahidol University2 个研究点 分布在 1 个国家目标入组 193 人开始时间: 2023年1月19日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
193
试验地点
2
主要终点
Pain interference

研究概览

简要总结

Cancer is the second leading cause of death worldwide, with approximately 18.1 million new cases and 9.6 million deaths reported in 2018. Cancer-related pain is experienced by 50-70% of patients, with a higher prevalence at advanced disease stages (66.4%). Since the development of WHO's cancer pain guidelines, several studies have reported good relief of symptoms and suffering for a majority of patients. Recent reports suggest that up to 50% of patients still report insufficient pain control. Patients with cancer often present with multiple symptoms and functional decline. Evidence supports multidisciplinary approaches to address symptoms and suffering, including early palliative care referral

From review literatures we found that the telemedicine group had significantly higher quality of life than the usual care group. In addition, the telemedicine group had lower anxiety and depression scores than the usual care group.

Therefore, we will conduct the non-randomized controlled study of using telemedicine comparing to conventional in-person at OPD in hospitalized cancer pain patients.

The purpose of this study is to assess the pain interference by using the Brief Pain Inventory (BPI) and to compare between the in-person group and the telemedicine group. To assess the cost-effectiveness of telemedicine for reducing symptoms associated with cancer and its treatment.

详细描述

The pain interference will be assessed and compared using Brief Pain Inventory from 0-70 between In-person group and telemedicine group at 1 month.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Age older than 18 years old
  • Cancer patients who new visit as out patient at pain clinic, Siriraj hospital

排除标准

  • Cannot read and write
  • Confusion
  • Unable to use the 0-10 Numerical Rating Scale (NRS) to rate pain intensity.
  • Unstable clinical presentation

研究组 & 干预措施

In-person

Active Comparator

Face to face at OPD

干预措施: In-person (Other)

Telemedicine

Experimental

Telemedicine

干预措施: Telemedicine (Other)

结局指标

主要结局

Pain interference

时间窗: at 1 month

The pain interference will be assessed and compared using Brief Pain Inventory from 0-70 between In-person group and telemedicine group.

次要结局

  • Quality of life (QoL)(at 1 month)
  • Pain intensity(at 1 month, 2 months and 3 months)
  • Functional status(At baseline, 1 month, 2 month, 3 month)
  • Opioid consumption(At baseline, 1 month, 2 month and 3 month)
  • Medication adverse effects(At baseline, 1-month, 2-month and 3-month)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验