Cognitive Training in the Virtual Reality Setting With Children Undergoing Radiotherapy for Brain Tumors

ConditionBrain Tumor
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age8-22
SponsorSt. Jude Children's Research Hospital

About this trial

The objective of this study is to estimate the feasibility and acceptability of cognitive training in the virtual reality setting with children undergoing radiotherapy for brain tumors. To achieve this goal, the investigators plan to study children undergoing radiotherapy for brain tumors randomly assigned to cognitive training administered via an iPad or virtual reality. Both groups will also participate in cognitive testing and exams using functional near infrared spectroscopy (fNIRS) pre- and post-intervention. The questions to be investigated are:

1. Will cognitive training via virtual reality be feasible and acceptable for children undergoing radiotherapy for brain tumors as indicated by participation rates, adherence and frequency of side effects? 2. Will cognitive training via virtual reality provide neurocognitive benefits? 3. Will there be predictable changes in brain activity as measured by neuroimaging?

Findings from this study will be used to develop a larger, definitive trial with direct potential to improve cognitive outcomes for children treated for cancer using a safe and effective alternative to desktop- or laptop-based computerized cognitive interventions with great promise for improving quality of life.

Eligibility criteria

Qualifiers

Initiating radiotherapy for a BT

Between 8-22 years of age at the time of enrollment

English or Spanish as the primary language

Research participant and one parent willing to participate and provide consent/assent according to institutional guidelines

Disqualifiers

Significant impairment in global intellectual functioning (estimated or full scale IQ < 70 based on standardized testing routinely conducted on primary treatment protocols or as part of the New Oncology Program in Psychology [NOPP])

History of significant neurological disease preceding BT diagnosis including stroke or head injury with loss of consciousness

Major sensory or motor impairment that would preclude valid cognitive testing secondary to inability to complete study procedures (e.g., blindness, paresis, poorly controlled seizures/photosensitive epilepsy, inadequate balance to sit or stand unassisted to complete cognitive training)

Psychiatric condition that would preclude or take precedence over study participation (e.g. active psychosis, suicidal ideation)

Trial design

Treatments tested in this trial

  • Cognitive training via iPad
  • Cognitive training via virtual reality

Treatment groups

45 Participants
are divided into 2 treatment groups