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Supportive Care for Patients With Hematological Malignancies Undergoing Hematopoietic Cell Transplant

Not Applicable
Completed
Conditions
Hematopoietic/Lymphoid Cancer
Interventions
Other: palliative care
Other: questionnaire administration
Procedure: quality-of-life assessment
Registration Number
NCT01758484
Lead Sponsor
Fred Hutchinson Cancer Center
Brief Summary

This pilot clinical trial studies supportive care for patients with hematological malignancies undergoing hematopoietic cell transplant. Supportive care may improve quality of life in this patient population.

Detailed Description

PRIMARY OBJECTIVES:

I. Pilot a supportive care intervention that begins prior to transplantation and continues through the acute peritransplant period.

II. Determine the proportion of patients who enroll and the level of comfort / distress of hematopoietic cell transplant (HCT) patients who meet with the supportive care team.

III. Pilot data collection mechanisms and cost retrieval in preparation for a randomized clinical trial.

OUTLINE:

Patients undergo supportive care consultation before transplantation and at least once monthly while they remain at the transplant center.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Written informed consent
  • English as primary language
  • Planned autologous or allogeneic hematopoietic cell transplantation
  • Presence of co-morbidities (hematopoietic cell transplant co-morbidity index [HCT-CI] score 3 or greater), high risk disease (relapse risk > 25%), or a planned type of transplant (human leukocyte antigen [HLA]-mismatched allogeneic or myeloablative) that places the patient at a higher than average risk of non-relapse mortality or relapse
Exclusion Criteria
  • Major psychiatric diagnosis that impairs cognitive functioning or is not controlled at the time of the approach, as judged by the patient's medical team
  • First transplant of a planned tandem procedure (the second transplant is eligible)

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Supportive care (palliative care support)quality-of-life assessmentPatients undergo palliative care support before transplantation and at least once monthly while they remain at the transplant center.
Supportive care (palliative care support)palliative carePatients undergo palliative care support before transplantation and at least once monthly while they remain at the transplant center.
Supportive care (palliative care support)questionnaire administrationPatients undergo palliative care support before transplantation and at least once monthly while they remain at the transplant center.
Primary Outcome Measures
NameTimeMethod
Study participation rates defined as the proportion of patients who consent to enrollUp to 5 months

Will mainly be descriptive.

Completion time for the supportive care consultationUp to 90 days post-treatment

Will mainly be descriptive.

Level of comfort / distress attributed to individual parts of the consultationUp to 90 days post-treatment

Will mainly be descriptive. The post-consultation scores measuring level of comfort or distress per topic in the supportive care consultation will be summarized per item.

Completeness of follow-up data collection, where completeness is defined by the proportion of instrument scores that can be calculated per given time pointUp to 90 days post-treatment

Will mainly be descriptive. The completeness of follow-up data collection will be calculated and reported as a proportion of successfully completed scales vs. scales attempted to be collected or completed by patients.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium

🇺🇸

Seattle, Washington, United States

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