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Telehealth Cognitive Training for Pediatric Cancer
Study Summary
This trial will explore a new telehealth training program to help kids with cancer and their caregivers. 10 kids and their caregivers will be enrolled at the University of Michigan.
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- I was treated for a brain tumor as a child.I am between 8 and 18 years old.I have a developmental, behavioral, or mood disorder that could affect my participation.I finished my last treatment over 6 months ago.I have had a traumatic brain injury or seizures in the past.
- Group 1: Intervention
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Does this medical trial have an upper age limit for participants?
"This research is currently admitting individuals aged 8 to 18 years old."
Are there any openings for participants in this experiment?
"The clinical trial in question is actively recruiting participants, as indicated on the official website. It was initially posted on January 1st 2023, and the most recent update was issued on January 19th of that same year."
How many individuals is this experimental protocol recruiting?
"Affirmative. Clinicaltrials.gov records indicate that this clinical trial was posted on January 1st, 2023 and most recently updated on the 19th of the same month. Right now, it is looking for 20 individuals to join from one medical site."
Who qualifies to partake in this research?
"This trial is recruiting 20 minors aged 8 to 18 who have previously received treatment for pediatric cancer. In order to qualify, participants must be fluent in English and demonstrate deficits in attention or executive functioning as evidenced by scores at least 1 standard deviation below the mean on cognitive tests like the CPT-3, Trail making Test A & B, Children's Category Test (CCT), and Wisconsin Card Sorting Test (WCST). Alternatively, they may display signs of executive function or attention problems during screening with a research assistant."
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