Social Cognition and Brain Integrity in Survivors of Pediatric Medulloblastoma



Status:Completed
Conditions:Brain Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:12 - 30
Updated:9/29/2018
Start Date:July 13, 2016
End Date:August 31, 2018

Use our guide to learn which trials are right for you!

Survivors of pediatric medulloblastoma (MB) are at-risk for neurocognitive and social
deficits, including specific skills such as facial affect recognition which is the ability to
recognize the emotional expressions of another person. Because the underlying mechanisms of
these deficits are poorly understood, the investigators propose to examine social-cognitive
skills (i.e. facial affect recognition) and indices of brain integrity, including an
established core neural network of face perception in MB survivors and healthy controls. By
comparing these outcomes between survivors of MB and healthy controls, investigators seek to
identify the areas of the brain that help individuals recognize emotions.

Primary Objective:

- To evaluate social cognition in adolescent and young adult survivors of pediatric
medulloblastoma.

Secondary Objective:

- To examine indices of brain integrity and function and their association with facial
affect recognition in survivors of pediatric medulloblastoma.

Comprehensive social-cognitive and behavioral data will be collected and structural and
functional brain imaging will be completed in an attempt to determine if disruptions to brain
integrity and function caused by prior treatment of medulloblastoma directly influence
social-cognition and behavior in survivors. These outcomes will be compared between survivors
and age-, gender-, and race-matched healthy community controls.

Participants who meet eligibility criteria and consent will undergo neurocognitive
(intelligence, attention, memory, processing speed, motor, executive function, and
visuospatial) and social cognitive evaluations (affect recognition, prosody, social memory,
withdrawal/isolation, loneliness, social anxiety, visuospatial, and executive function).
Functional magnetic resonance imaging (fMRI) will be completed during affect identification
tasks to assess activation of the core face perception network. Magnetic resonance with
diffusion tensor imaging (DTI) will be obtained to quantify water diffusion within white
matter tracts to assess white matter integrity and its association with functional outcomes.

Inclusion Criteria - Medulloblastoma Survivors:

- Enrolled on the SJLIFE protocol at St. Jude Children's Research Hospital (SJCRH).

- Completed treatment for medulloblastoma at SJCRH.

- Infratentorial tumor location.

- Treated with craniospinal irradiation.

- ≥ 5 years post diagnosis.

- Between 12 and 30 years of age at time of enrollment.

- English speaking.

Inclusion Criteria - Controls:

- Enrolled on the SJLIFE protocol as a community control.

- Between 12 and 30 years of age at time of enrollment.

- English speaking.

Exclusion Criteria - Medulloblastoma Survivors:

- Diagnosis of a genetic disorder/pre-existing neurodevelopmental condition associated
with neurocognitive or social impairment (e.g., down syndrome, autism).

- History of head injury associated with neurocognitive impairment.

- Diagnosis of a serious psychiatric condition associated with neurocognitive or social
morbidities (e.g. schizophrenia).

- Currently pregnant (due to MRI studies).

- Implanted metal unsafe for MRI or medical device (i.e. pacemaker)

- Requires sedation to complete MRI.

- Legally blind or unaidable hearing loss.

- Treated for medulloblastoma <3 years of age

- Received re-irradiation to the brain.

- Completed SJLIFE HPP-19 (pilot study) at SJCRH.

Exclusion Criteria - Controls:

- No history of childhood cancer or cancer related therapy.

- First degree relative or direct friend of medulloblastoma participant.

- Diagnosis of a genetic disorder/neurodevelopmental condition associated with
neurocognitive or social impairment (e.g., down syndrome, autism).

- History of head injury associated with neurocognitive impairment.

- Diagnosis of a serious psychiatric condition associated with neurocognitive or social
morbidities (e.g. schizophrenia).

- Currently pregnant (due to MRI studies).

- Implanted metal unsafe for MRI or medical device (i.e. pacemaker).

- Requires sedation to complete MRI.

- Legally blind or unaidable hearing loss.
We found this trial at
1
site
262 Danny Thomas Pl
Memphis, Tennessee 38105
(901) 495-3300
Principal Investigator: Tara Brinkman, PhD
Phone: 866-278-5833
St. Jude Children's Research Hospital St. Jude is unlike any other pediatric treatment and research...
?
mi
from
Memphis, TN
Click here to add this to my saved trials