Risk of Fatigue in Adolescent and Young Adult Hodgkin Lymphoma Patients
NCT ID: NCT01228461
Last Updated: 2017-04-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
10 participants
OBSERVATIONAL
2010-02-28
2012-01-31
Brief Summary
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The proposed research will utilize Vanderbilt-Ingram Cancer Center REACH for Survivorship Program together with the investigators Hematologic Malignancies Program. In adolescent and young adults (AYA), ages 18 - 39 the investigators will address the following:
Primary Aims Aim 1: Assess the prevalence and severity of fatigue and its impact on functional outcomes Aim 2: Determine host, disease and treatment-related risk factors for fatigue
Secondary Aims Aim 1: Evaluate the association between levels of proinflammatory cytokine activity and fatigue Aim 2: Evaluate the association between fatigue and self reported fatigue in AYA Hodgkin lymphoma (HL) survivors.
Hypotheses:
1. Fatigue is more prevalent and severe among AYA HL patients and survivors, compared to general population and will be associated with impaired functional outcome.
2. Risk factors for fatigue include higher disease stage, B symptoms and elevated erythrocyte sedimentation rate at diagnosis, dose density of chemotherapy and higher doses and more expanded fields of radiotherapy.
3. Risk of fatigue is associated with long-term cardiopulmonary and endocrine complications.
4. Levels of specified proinflammatory cytokines are associated with increased fatigue.
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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AYA with Fatigue and Hodgkin Lymphoma
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Alive without evidence of recurrent disease
* Must be off therapy (not on active treatment for HL or other malignancies)
* Must not be on any form of chemotherapy (oral or intravenous \[IV\])
* Provide informed consent
* Can read and understand English
* Treated with risk-adapted therapy which may include radiotherapy doses \< 30 Gy
Exclusion Criteria
15 Years
39 Years
ALL
No
Sponsors
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Vanderbilt University
OTHER
Responsible Party
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Locations
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Vanderbilt University Medical Center
Nashville, Tennessee, United States
Countries
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Other Identifiers
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091550
Identifier Type: -
Identifier Source: org_study_id
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