HEME Home Transfusion Program

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorDana-Farber Cancer Institute

About this trial

This research study is evaluating whether a new care delivery program that provides access to home blood transfusions in hospice (i.e, HEME-Hospice) compared to regular standard of care improves quality of life, mood, and end-of-life health care utilization for patients with hematologic malignancies.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of a relapsed/refractory 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 severe transfusion reaction

Disqualifiers

Age < 18 years

Already enrolled in hospice

Resides in nursing home or assisted living facility

History of previous serious adverse transfusion reaction

Trial design

Design model

Parallel

Treatments tested in this trial

  • HEME-Hospice Program

    Behavioral

    A care delivery program that combines home-based transfusions with routine home hospice care. Transfusions are administered by trained transfusion nurses. Standard hospice care is provided by an interdisciplinary team of non-transfusion nurse case managers, hospice aides, social workers, and chaplains.

Treatment groups

700 Participants
are divided into 2 treatment groups
Group A: Arm 1: Access to home blood transfusions while enrolled in hospice (HEME-Hospice care)Experimental treatment 1 intervention
Group B: Arm 2: Usual CareNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Hospice Enrollment Rate

Establish that hospice enrollment rate is higher with access to HEME-Hospice versus usual care.

Time frame
6 months
2

Length of Hospice Enrollment

Number of days from hospice enrollment to date of death or hospice disenrollment

Time frame
6 months

Secondary outcomes

1

Chemotherapy Utilization in the Last 14 Days of Life

Compare chemotherapy use in the last 14 days of life between those with access to HEME-Hospice versus usual care

Time frame
Last 14 days of life
2

Hospitalization Rate

Compare hospitalization (2 or more hospitalizations) in the last 30 days of life between those with access to HEME-Hospice versus usual care

Time frame
Last 30 days of life
3

Intensive care unit (ICU) Admission Rate

Compare ICU admission in the last 30 days of life between those with access to HEME-Hospice versus usual care

Time frame
Last 30 days of life
4

Hospital Death

Compare occurrence of death in the hospital between those with access to HEME-Hospice versus usual care

Time frame
Last 30 days of life

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Dana-Farber Cancer Institute

Lead sponsor

National Cancer Institute (NCI)

Collaborator