Actively Recruiting
Feasibility and Efficacy of Attentional-Control Training Using EndeavorRx to Support Children with Sickle Cell Disease Aged 8 to 16 Receiving Chronic Blood Transfusions
Led by Children's National Research Institute · Updated on 2025-01-10
20
Participants Needed
1
Research Sites
153 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Children with sickle cell disease (SCD) often have lower cognitive abilities, especially trouble with attention, compared to peers without SCD. These difficulties are related to brain damage caused by strokes and anemia common in severe SCD cases, affecting areas responsible for executive function and attention. This research is exploring if EndeavorRx, an FDA-approved digital attention training program, can help improve attention in children with SCD aged 8 to 16 who are on chronic blood transfusion therapy to prevent strokes. EndeavorRx is delivered as a tablet-based video game that trains attention skills through interactive tasks. Children play for 25 to 30 minutes daily, five days a week, over four weeks. The program includes two main tasks: responding to target stimuli while ignoring distractions and steering a hovercraft to hit or avoid objects. The game adjusts its difficulty based on the user's performance both during and between sessions to continuously challenge attention control. Participants will be monitored for about 10 months to assess how interested families are in the program, how often children complete the training, and their satisfaction with its ease of use. Researchers will also collect data on attention improvements during the four-week intervention. The study involves 20 children with SCD, with assessments including attention tests and parent reports to evaluate the program's feasibility and preliminary effects.
CONDITIONS
Official Title
Feasibility and Efficacy of Attentional-Control Training in Sickle Cell Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of sickle cell disease
- Age between 8 and 16 years
- Receiving monthly blood transfusions consistently for at least 3 months
- T-score above the 75th percentile for Omission Errors on the Conners' Continuous Performance Test, 3rd Edition (CPT-3) or for the Inattention subscale of the ADHD Rating Scale, Fifth Edition (ADHD-RS-V)
You will not qualify if you...
- Estimated Intelligence Quotient below 70
- Motor, visual, or auditory impairment that prevents computer use
- Known mental health diagnosis that precludes or takes priority over cognitive training
- History of photosensitive seizures
- Insufficient English fluency
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Children's National Hospital
Washington D.C., District of Columbia, United States, 20010
Actively Recruiting
Research Team
S
Steven J Hardy, Ph.D.
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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