Understanding the Late Effects of Surviving a Pediatric Brain Tumor
Status: | Recruiting |
---|---|
Conditions: | Cancer, Cancer, Brain Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 6 - 16 |
Updated: | 8/24/2018 |
Start Date: | June 28, 2017 |
End Date: | June 2019 |
Contact: | Stephen Sands, PsyD |
Email: | sandss@mskcc.org |
Phone: | 646-888-0023 |
Biological Substrates of Impaired Neurocognitive Functioning: Understanding the Late Effects of Surviving a Pediatric Brain Tumor
The goal of this study is to learn about the cognitive and behavioral functioning of children
being treated for cancer.
being treated for cancer.
Inclusion Criteria:
Children Treated for Posterior Fossa Tumors:
- As per medical record or clinical report, successfully completed all medical treatment
for either an M0 posterior fossa medulloblastoma without dissemination or posterior
fossa low-grade astrocytoma without relapse or evidence of residual disease.
- For medulloblastoma survivors only: Previously treated with gross total resection
(GTR), craniospinal irradiation with conformal posterior fossa boost radiotherapy (CSI
+ Boost) and chemotherapy
- For low grade astrocytoma survivors only: Previously treated with gross total
resection ONLY (no chemotherapy or radiotherapy).
- As per medical record or clinician report, between 1-10 years post completion of their
medical treatment for their posterior fossa brain tumor.
- Subject is between the ages of 6 through 16 years at time of consent.
- As per medical record or parent report, subject is able to tolerate an MRI without
sedation.
Healthy Control Participants:
- No major medical illness, as determined by medical interview by study physician.
- As per parent report, subject is between the ages of 6 through 16 years at time of
consent.
- As per parent report, subject is able to tolerate an MRI without sedation.
Exclusion Criteria:
All Participants:
- Full Scale IQ as documented to be below a standard score of <70 based upon the study
IQ assessment completed after consent.
- As per self or parent report, completed any portion of the neuropsychological battery
used in this study within the last year.
- MRI contraindications (e.g., implanted ferromagnetic devices, claustrophobia) as per
radiology clinical operating procedures.
- As per self or parent report or medical record, currently taking medications that have
CNS effects (i.e., antidepressants, neuroleptics, anti-seizure medications, drugs that
affect blood pressure or heart rate, alpha-agonists, adrenergic blockers, lithium,
sedating antihistamines, and some medications for the treatment of asthma).
- As per self or parent report, non-fluency in English language as demonstrated by
current educational placement in a non-English-speaking classroom setting.
We found this trial at
3
sites
1801 Inwood Rd
Dallas, Texas 75390
Dallas, Texas 75390
(214) 645-3300
Phone: 214-730-5437
University of Texas Southwestern Medical Center UT Southwestern is an academic medical center, world-renowned for...
Click here to add this to my saved trials
1275 York Ave
New York, New York 10021
New York, New York 10021
(212) 639-2000
Principal Investigator: Stephen Sands, PsyD
Phone: 646-888-0023
Memorial Sloan Kettering Cancer Center Memorial Sloan Kettering Cancer Center — the world's oldest and...
Click here to add this to my saved trials
4800 Sand Point Way NE
Seattle, Washington 98105
Seattle, Washington 98105
(206) 987-2000
Principal Investigator: Dennis W Shaw, MD
Phone: 206-987-2134
Seattle Children's Hospital Seattle Children’s Hospital specializes in meeting the unique physical, emotional and developmental...
Click here to add this to my saved trials