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Clinical Trials/NCT03641378
NCT03641378CompletedNot Applicable

Multi-Site Randomized Trial of Inpatient Palliative Care for Patients With Hematologic Malignancies Undergoing Hematopoietic Stem Cell Transplantation

Massachusetts General Hospital3 sites in 1 country546 target enrollmentStarted: September 30, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
546
Locations
3
Primary Endpoint
Patient-reported Quality of Life (QOL): Functional Assessment of Cancer Therapy - Bone Marrow Transplant (FACT-BMT)

Study Overview

Brief Summary

This research study is evaluating the impact of early involvement of a palliative care team working with the transplant oncology team will have on the quality of life, symptoms, and mood of patients undergoing stem cell transplantation.

Detailed Description

The Participant has a type of blood cancer and will be undergoing stem cell transplantation. Frequently people undergoing stem cell transplantation experience physical and emotional symptoms during the course of their hospitalization for stem cell transplantation. These can be very distressing to both patient and the family members. The study doctors want to know if the early introduction of a team of clinicians that specialize in the lessening (palliation) of many of these distressing symptoms may improve the participant overall care.

This team of clinicians is called the palliative care team and they focus on ways to improve the participant pain and other symptom management (nausea, fatigue, shortness of breath, anxiety, etc.) and to assist the participant and the participant's family in coping with the emotional and social issues associated with your diagnosis. The team consists of physicians and advance practice nurses who have been specially trained in the care of patients facing serious illness.

The main purpose of this study is to compare two types of care - standard transplant oncology care and standard transplant oncology care with early involvement of palliative care clinicians to see which is better for improving the experience of patients and families with blood cancers undergoing stem cell transplantation.

The purpose of this research study is to find out whether introducing patients and families undergoing stem cell transplantation to the palliative care team that specializes in symptom management can improve the physical and psychological symptoms that patients and families experience during hospitalization for stem cell transplantation.

The study will use a series of questionnaires to measure the participant and the participant 's caregivers' quality of life, physical symptoms, and mood. Study questionnaires will be completed in the hospital or clinic with assistance provided as need.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patient Inclusion Criteria
  • •adult patients (≥ 18 years) with hematologic malignancy admitted for autologous or allogeneic HCT.
  • •ability to read and respond to questions in English or Spanish or to complete questionnaires with assistance from an interpreter.
  • •Caregiver Eligibility Criteria:
  • •adult (≥ 18 years) relative or a friend of a patient who agrees to participate in the study whom the patient identified as living with them or having in-person contact with him or her at least twice per week.
  • •ability to read and respond to questions in English or Spanish or to complete questionnaires with the assistance of an interpreter.

Exclusion Criteria

  • •Patient Exclusion Criteria
  • •Patients undergoing HCT for benign hematologic conditions
  • •Patients undergoing outpatient HCT.
  • •Patients with psychiatric or cognitive conditions which the treating clinicians believes prohibits compliance with study procedures

Arms & Interventions

Inpatient Palliative Care Intervention

Experimental
  • Patients and Caregivers will complete baseline self-report assessments at the time of obtaining informed consent
  • Palliative Care Intervention
  • Therapeutic Relationship

--Develop a strong therapeutic relationship with patients and caregivers

  • Assessment and Treatment of Patient Symptoms

--Clarify the symptoms the patient will likely experience and offer reassurance about the methods for reporting and treating symptoms

  • Managing Patients and Caregivers Expectations

--Address early on patients and caregivers' concerns about the trajectory of illness during HCT and treatment side effects

  • Coping with Illness and HCT --Introduce strategies to help improve adjustment (e.g., behavioral, cognitive, and spiritual approaches; accepting illness while maintaining hope; social support)

Intervention: Palliative Care Intervention (Other)

Transplant Care Alone

Experimental
  • Patients and Caregivers will complete baseline self-report assessments at the time of obtaining informed consent.
  • Standard Transplant Care

Intervention: Standard Transplant Care (Other)

Outcomes

Primary Outcomes

Patient-reported Quality of Life (QOL): Functional Assessment of Cancer Therapy - Bone Marrow Transplant (FACT-BMT)

Time Frame: 2 weeks

Compare patient QOL using the Functional Assessment of Cancer Therapy- Bone Marrow Transplant (FACT-BMT) scores at week 2 between the study groups Score range 0-164 with higher score indicating better quality of life

Secondary Outcomes

  • Patients' Quality of Life (QOL) Longitudinally: FACT-BMT(up to 6 months)
  • Patients' Symptom Burden(up to 6 months)
  • Patients' Post-traumatic Stress Symptoms (PTSD)(up to 6 months)
  • Caregiver QOL: CARGOQOL(up to 6 months)
  • Patients' Psychological Distress(up to 6 months)
  • Patients' Depression(up to 6 months)
  • Patients' Fatigue(up to 6 months)
  • Caregiver Psychological Distress(up to 6 months)
  • Caregiver Depression(up to 6 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

El-Jawahri, Areej,M.D.

Principal Investigator

Massachusetts General Hospital

Study Sites (3)

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