Actively Recruiting

Phase Not Applicable
Age: 8Years - 22Years
All Genders
NCT05947045

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

Led by St. Jude Children's Research Hospital · Updated on 2026-04-23

45

Participants Needed

1

Research Sites

192 weeks

Total Duration

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AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 8Years - 22Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Initiating radiotherapy for a brain tumor
  • Between 8 and 22 years of age at enrollment
  • English or Spanish as the primary language
  • Participant and one parent willing to participate and provide consent/assent
  • Participant willing to take part in required cognitive training sessions
Not Eligible

You will not qualify if you...

  • Significant intellectual impairment with IQ below 70
  • History of serious neurological disease before brain tumor diagnosis, such as stroke or head injury with loss of consciousness
  • Major sensory or motor impairment preventing valid cognitive testing (e.g., blindness, paralysis, poorly controlled seizures, inability to balance to complete training)
  • Psychiatric conditions that prevent or take precedence over study participation (e.g., active psychosis, suicidal thoughts)
  • Need for general anesthesia during radiation therapy (participation allowed if only sedated for planning but not daily treatment)

AI-Screening

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Trial Site Locations

Total: 1 location

1

St. Jude Children's Research Hospital

Memphis, Tennessee, United States, 38105

Actively Recruiting

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Research Team

H

Heather Conklin, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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