跳至主要内容
临床试验/NCT03396510
NCT03396510已完成不适用

Electronic Symptom Monitoring Intervention for Hospitalized Patients With Cancer

Massachusetts General Hospital2 个研究点 分布在 1 个国家目标入组 390 人开始时间: 2018年2月12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
390
试验地点
2
主要终点
Proportion of days with improved symptoms between study arms

研究概览

简要总结

This research study is evaluating a new way to deliver oncology care for patients with cancer

详细描述

Patients with cancer may experience a considerable symptom burden, often requiring hospitalizations for symptom management. The study doctors want to know if daily electronic monitoring of the symptoms, such as pain, nausea, constipation, and diarrhea may improve care while participants are hospitalized.

The goal of this study is to evaluate a new way to deliver oncology care where patients' symptoms are systematically monitored during their hospital admission. The investigators are studying whether patients whose clinicians receive their patients' detailed symptom reports each day have improved symptom management compared to those whose clinicians do not receive their patients' detailed symptom reports each day.

The study will use questionnaires to measure the participant symptoms and involves participating in a study for as long as the participants are admitted to the hospital. The information the investigators collect will help them determine if electronic symptom monitoring improves the care of patients with cancer

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 or older
  • Diagnosed with advanced cancer (defined as receiving treatment with palliative intent as per chemotherapy order entry designation, oncology clinic notes, and/or trial consent forms, or not receiving chemotherapy but followed for incurable disease as per oncology clinic notes)
  • Admitted to the oncology service at Massachusetts General Hospital
  • Verbal fluency in English

排除标准

  • Unwilling or unable to participate in the study
  • Admitted electively
  • Participated during a previous admission

结局指标

主要结局

Proportion of days with improved symptoms between study arms

时间窗: 2 years

Using ESAS and PHQ symptoms, the investigators will compare the proportion of days that symptoms improved in standard care versus IMPROVED.

次要结局

  • Proportion of days with worsened symptoms between study arms(2 years)
  • Hospital readmissions within 90 days of prior hospital discharge between study arms(90 days)
  • Change in patients' symptom scores from baseline to discharge(2 years)
  • Hospital readmissions within 30 days of prior hospital discharge between study arms(30 days)
  • Hospital length of stay (measured continuously as days admitted to the hospital) between study arms(2 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ryan Nipp

Principal Investigator

Massachusetts General Hospital

研究点 (2)

Loading locations...

相似试验