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NCT05704790
Feasibility and Acceptability of Brief, Telehealth Cognitive Compensatory Training for Pediatric Cancer Patients
Conditions: Pediatric Cancer
Sex: All
Ages: 8 Years – 18 Years
Phase: NA
Enrollment: 20
Sponsor: University of Michigan Rogel Cancer Center
Location: United States
Summary
This pilot study will be a prospective, single arm study to investigate the feasibility and acceptability of a brief, telehealth, cognitive compensatory training intervention for children with a history of pediatric cancer at the University of Michigan.
Study aims to enroll 10 children with a history of treatment for pediatric cancer, along with their caregiver.
Eligibility Criteria
Inclusion Criteria:Patient between the ages of 8 and 18Patient has a history of pediatric cancerPatient is at least 6 months posttreatment completionPatient and caregiver are fluent in English, as intervention materials are only available in English at this time.Patient demonstrates deficits in attention and/or executive functioning as evidenced by either (a) performance below one standard deviation on at least one cognitive measure of attention or executive functioning, such as on the Conners Continuous Performance Test (CPT-3), Trail making Test A & B, Children's Category Test (CCT), and Wisconsin Card Sorting Test (WCST) and/or (b) executive functioning and attention problems are identified during screening with the research assistant.Exclusion Criteria:Patient has a history of treatment for a pediatric brain tumorPatient has a history of traumatic brain injury or seizuresPatient has a history of a developmental disorder (i.e., autism, intellectual disability), behavioral disorder (i.e., oppositional defiant disorder, conduct disorder), or mood disorder (i.e., disruptive mood dysregulation disorder) that would negatively interfere with patient's participation in the intervention.
Source: ClinicalTrials.gov (NCT05704790). StuddyBuddy aggregates publicly available trial information.