Last updated on September 2011

Collecting and Storing Information From Patients With Cancer or Other Chronic Disease Who Have Undergone Neurobehavioral Assessments on Another Clinical Trial


Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Unspecified Childhood Solid Tumor | Cognitive/Functional Effects | Psychosocial Effects of Cancer and Its Treatment | Lymphoma | Leukemia | Unspecified Adult Solid Tumor | Long-term Effects Secondary to Cancer Therapy in Children | Metastatic Cancer | Long-term Effects Secondary to Cancer Therapy in Adults | Brain and Central Nervous System Tumors | Neurofibromatosis Type 1 | Protocol Specific
  • Age: - 100 Years
  • Gender: Male or Female
  • Other:
    DISEASE CHARACTERISTICS:
    Any of the following diagnoses are allowed:
    HIV positivity
    Cancer (especially brain tumors and leukemia)
    Neurofibromatosis type 1
    Data obtained from infants, children, adolescents, and adults who underwent
    neurobehavioral assessments as part of a past, current, or future IRB-approved
    protocol
    No CNS condition (i.e., Down syndrome, severe intraventricular hemorrhage) not
    related to primary medical diagnosis (i.e., HIV, cancer) that may affect
    neurobehavioral functioning, missing values on a particular test being studied, or
    invalid data as determined by the investigator
    PATIENT CHARACTERISTICS:
    Not specified
    PRIOR CONCURRENT THERAPY:
    Not specified

Recruitment Status: Open


Brief Description Eligibility Contact Research Team


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