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临床试验/NCT05509439
NCT05509439已完成不适用

A Home Transfusion Program for Patients With Advanced Hematologic Malignancies

Dana-Farber Cancer Institute2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2024年10月18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
10
试验地点
2
主要终点
Enrollment Rate

研究概览

简要总结

The purpose of the research is to assess the feasibility and acceptability of a home blood transfusion program for patients with hematologic malignancies who need blood transfusions

详细描述

This feasibility study will be used to assess the feasibility and acceptability of a hospice-embedded home transfusion program to patients with hematologic malignancies. All enrolled subjects will be patients cared for at Dana Farber Cancer Institute.

This study is a single-arm study of 10 patients with advanced hematologic malignancies who have a limited life-expectancy of six months or fewer and are hospice eligible.

10 Caregivers of enrolled patients will also be invited to participate if interested.

This research study involves completing questionnaires, a brief interview, blood draws, and blood transfusions when needed.

Participants will be in the research study for up to six months.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
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

  • Patients with advanced hematologic malignancies:
  • Diagnosis of a hematologic malignancy
  • Age ≥ 18 years
  • Receipt of primary oncologic care at DFCI (at least 2 outpatient visits in 12 months prior to enrollment)
  • Has received at least one red blood cell (RBC) or platelet transfusion since blood cancer diagnosis in the clinic or hospital setting without a serious adverse transfusion reaction
  • Physician-estimated prognosis of six months or less
  • Has an adult informal caregiver that lives in the same residence
  • Patient resides within catchment served by Care Dimensions Hospice
  • Caregivers:
  • Identified informal caregiver of enrolled patient with hematologic malignancy
  • Age ≥ 18 years

排除标准

  • Age < 18 years
  • Does not have an identified adult informal caregiver who lives in the same residence
  • History of previous serious adverse transfusion reaction
  • Presence of decompensated congestive heart failure
  • Caregiver
  • Age < 18 years
  • Our study will exclude members of the following special populations:
  • Adults unable to consent
  • Individuals who are not yet adults (infants, children, teenagers)
  • Pregnant women
  • Prisoners

结局指标

主要结局

Enrollment Rate

时间窗: 6 months

Number of patients consented to the study divided by eligible patients approached by the study team

Completion of Home Transfusions and Patient-Reported Data

时间窗: 6 months

Proportion of completed home transfusions among enrolled patients who meet transfusion criteria, and proportion of enrolled patients who complete patient-reported data collection

次要结局

  • Satisfaction Rate(3 Weeks)
  • Disenrollment Rate(6 months)

研究者

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

Oreofe Odejide, MD

Principal Investigator

Dana-Farber Cancer Institute

研究点 (2)

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