Quality of Life in Younger Leukemia and Lymphoma Survivors
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|ClinicalTrials.gov Identifier: NCT00956475|
Recruitment Status : Completed
First Posted : August 11, 2009
Last Update Posted : August 24, 2011
RATIONALE: Collecting information about the effect of hematologic cancer and its treatment on quality of life may help doctors learn more about the disease and plan the best treatment.
PURPOSE: This phase I trial is studying quality of life in younger leukemia and lymphoma survivors.
|Condition or disease||Intervention/treatment|
|Anxiety Disorder Cancer Survivor Fatigue Leukemia Long-term Effects Secondary to Cancer Therapy in Adults Lymphoma Lymphoproliferative Disorder Pain Psychosocial Effects of Cancer and Its Treatment Small Intestine Cancer||Behavioral: telephone-based intervention Other: questionnaire administration Procedure: assessment of therapy complications Procedure: fatigue assessment and management Procedure: psychosocial assessment and care Procedure: quality-of-life assessment|
- To collect preliminary data to determine the extent to which there is impairment in quality of life of young adult survivors of hematologic malignancies.
- To identify the most common areas of concern in these survivors.
- To explore patterns of quality-of-life impairment associated with age, gender, and type of treatment (transplant vs non-transplant) in these survivors.
OUTLINE: Patients are assessed in a telephone interview using a brief demographic and clinical data form. Patients then undergo quality-of-life assessment by the Cancer Patient/Cancer Survivor Version questionnaire via telephone.
|Study Type :||Observational|
|Actual Enrollment :||48 participants|
|Official Title:||Quality of Life in Young Adult Survivors of Hematologic Malignancies|
|Study Start Date :||October 2008|
|Actual Primary Completion Date :||September 2010|
|Actual Study Completion Date :||August 2011|
Behavioral: telephone-based intervention
- Quality of life [ Time Frame: 1-10 years after treatment ]
- Most common areas of concern [ Time Frame: 1-10 years after treatment ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00956475
|United States, Ohio|
|Case Medical Center, University Hospitals Seidman Cancer Center, Case Comprehensive Cancer Center|
|Cleveland, Ohio, United States, 44106-5065|
|Principal Investigator:||Regan Demshar, RN||Case Medical Center, University Hospitals Seidman Cancer Center, Case Comprehensive Cancer Center|