← Back to Search

Behavioural Intervention

Telehealth Cognitive Training for Pediatric Cancer

N/A
Recruiting
Led By Kaitlin McCloskey
Research Sponsored by University of Michigan Rogel Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 weeks from trial entry
Awards & highlights

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.

Who is the study for?
This trial is for children aged 8-18 who have completed cancer treatment at least 6 months ago, show attention or executive functioning deficits, and can speak English. It's not for those with developmental, behavioral, mood disorders, traumatic brain injury or seizures, or a history of pediatric brain tumor.Check my eligibility
What is being tested?
The study tests a telehealth cognitive training program designed to help kids who've had cancer improve their attention and problem-solving skills. It involves the child and caregiver in a single group without comparison to other treatments.See study design
What are the potential side effects?
Since this is a non-medical intervention focusing on cognitive training via telehealth sessions, there are no direct physical side effects like you'd expect from medication; however, participants may experience fatigue or frustration.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 weeks from trial entry
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6 weeks from trial entry for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Determining satisfaction and perceived benefit from study intervention based off of change in results from the BRIEF-2 questionnaire from baseline to 6 weeks post trial entry
Determining satisfaction and perceived benefit from study intervention based off of change in results from the Conners 3 questionnaire from baseline to 6 weeks post trial entry
Determining satisfaction and perceived benefit from study intervention based off of change in results from the PKEQ questionnaire from baseline to 6 weeks post trial entry
+2 more
Other outcome measures
Clinical outcomes based off of response to the BRIEF-2 study questionnaire
Clinical outcomes based off of response to the Conners 3 study questionnaire
Clinical outcomes based off of response to the PKEQ study questionnaire
+3 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: InterventionExperimental Treatment1 Intervention
The intervention will include 5 weekly sessions (60-90 minutes each) of cognitive compensatory training (CCT) delivered virtually by a pediatric neuropsychologist.

Find a Location

Who is running the clinical trial?

University of Michigan Rogel Cancer CenterLead Sponsor
294 Previous Clinical Trials
24,251 Total Patients Enrolled
Kaitlin McCloskeyPrincipal InvestigatorUniversity of Michigan Rogel Cancer Center

Media Library

Cognitive Compensatory Training (Behavioural Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05704790 — N/A
Pediatric Cancer Research Study Groups: Intervention
Pediatric Cancer Clinical Trial 2023: Cognitive Compensatory Training Highlights & Side Effects. Trial Name: NCT05704790 — N/A
Cognitive Compensatory Training (Behavioural Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05704790 — N/A
~9 spots leftby Jun 2025
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Back to top