Feasibility/Acceptability of Attentional-Control Training in Survivors

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age8-16
SponsorChildren's National Research Institute

About this trial

This is a multicenter pilot randomized controlled trial, with an active control condition, of the feasibility, acceptability, and preliminary efficacy of EndeavorRx in a cohort of survivors of acute lymphoblastic leukemia or brain tumor ages 8-16 who are \> 1 year from the end of therapy.

Eligibility criteria

Qualifiers

Aged 8-16 years at time of screening.

History of diagnosis of acute lymphoblastic leukemia (ALL) or brain tumor (BT).

At least 1 year from completion of planned therapy and stable from a disease standpoint.

Participating child and caregiver are fluent in spoken English.

Disqualifiers

A history of photosensitive seizures.

A motor, visual, or auditory handicap that prevents computer use.

A mental health condition that precludes, or takes treatment precedence over, participation in the cognitive training.

Participants identified during the baseline assessment as having a full-scale IQ < 80, as estimated by WASI-II (Vocabulary and Matrix Reasoning), will not be randomized.

Trial design

Treatments tested in this trial

  • EndeavorRx
  • Control video game

Treatment groups

50 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Children's National Research Institute

Lead sponsor

St. Jude Children's Research Hospital

Collaborator

Children's Hospital of Philadelphia

Collaborator

George Washington University

Collaborator

National Cancer Institute (NCI)

Collaborator