Supportive Oncology Care at Home Intervention for Patients With Lymphoma
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 3
- 试验地点
- 2
- 主要终点
- enrollment rate
研究概览
简要总结
The goal of this research is to evaluate an intervention, which the investigators call "Home Hospital for Lymphoma," that involves remote patient monitoring and home-based supportive care for patients hospitalized with lymphoma at Massachusetts General Hospital.
详细描述
This research study is a single arm pilot Feasibility Study, which is the first-time investigators are examining this hospital at home intervention for patients with lymphoma.
The research study procedures include screening for eligibility, questionnaires, remote patient monitoring (e.g. patient-reported symptoms and home monitored vital signs) and home-based supportive care (e.g. visits to patients' homes to address and manage any concerning issues identified), and interviews of participants, caregivers, and clinicians asking their perceptions of the Home Hospital for Lymphoma program.
Participants will include 3 groups:
Enrolled participants receiving the hospital at home intervention, caregivers of participants, and clinicians.
Participants will be in the research study for about six months after consent. It is expected that up to 38 participants will take part in this research study.
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
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age 18 or older
- •Receiving their lymphoma care with curative intent at MGH (treatment intent based upon chemotherapy order in the electronic medical record)
- •Hemodynamically stable during the first 24 hours of hospital admission at MGH
- •Residing within the designated geographic area for MGH Home Hospital Service (an approximately 10-mile radius from MGH)
- •Able to communicate and respond to questionnaires in English
- •Lives with a family member or a friend who supports the patient at home
- •Deemed eligible for supportive oncology care at home based on the MGH Home Hospital clinician evaluation
排除标准
- •Those admitted to the intensive care unit
- •Have high oxygen requirement (FIO2 > 0.4)
- •Experience active angina or cardiac arrythmias
- •Have a planned inpatient surgical or interventional procedure
- •Have uncontrolled psychiatric illness or impaired cognition that prohibits complying with the study procedures
- •Have uncontrolled pain requiring intravenous pain medications
- •Those deemed ineligible based on the Home Hospital Service clinician evaluation
结局指标
主要结局
enrollment rate
时间窗: 1 year
The primary endpoint is feasibility. The proposed intervention will be deemed feasible if at least 60% of eligible patients are enrolled in the study
retention rate
时间窗: 1 year
The primary endpoint is feasibility. The proposed intervention will be deemed feasible if those enrolled patients complete at least 60% of daily patient-reported symptom assessment.
次要结局
- Rates of completion of daily vital signs(1 year)
- Acceptability of the intervention(1 year)
- Rates of Adverse Events(1 year)
研究者
El-Jawahri, Areej,M.D.
Principal Investigator
Massachusetts General Hospital