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| ID | Type | Description | Link |
|---|---|---|---|
| NCI-2012-03009 | Registry Identifier | CTRP (Clinical Trial Reporting Program) | |
| P30CA015704 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Cancer Institute (NCI) | NIH |
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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Supportive care (palliative care support) | Experimental | Patients undergo palliative care support before transplantation and at least once monthly while they remain at the transplant center. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| palliative care | Other | Undergo supportive care intervention |
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| Measure | Description | Time Frame |
|---|---|---|
| Study participation rates defined as the proportion of patients who consent to enroll | Will mainly be descriptive. | Up to 5 months |
| Completion time for the supportive care consultation | Will mainly be descriptive. | Up to 90 days post-treatment |
| Level of comfort / distress attributed to individual parts of the consultation | 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. | Up to 90 days post-treatment |
| Completeness of follow-up data collection, where completeness is defined by the proportion of instrument scores that can be calculated per given time point | 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. | Up to 90 days post-treatment |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Stephanie Lee | Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium | Seattle | Washington | 98109 | United States |
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| ID | Term |
|---|---|
| D019337 | Hematologic Neoplasms |
| ID | Term |
|---|---|
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
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| ID | Term |
|---|---|
| D010166 | Palliative Care |
| ID | Term |
|---|---|
| D005791 | Patient Care |
| D013812 | Therapeutics |
| D006296 | Health Services |
| D005159 | Health Care Facilities Workforce and Services |
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| questionnaire administration |
| Other |
Ancillary studies |
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| quality-of-life assessment | Procedure | Ancillary studies |
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