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Study of Computer Attention Training Programs in Schools for Children With Attention Deficit/Hyperactivity Disorder

Randomized Control Trial of Two Computer-Based Attention Training Programs in Schools for Children With Attention Deficit/Hyperactivity Disorder (ADHD)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01583829
Acronym
CATS
Enrollment
104
Registered
2012-04-24
Start date
2009-05-31
Completion date
2013-11-30
Last updated
2017-07-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Attention Deficit Hyperactivity Disorder

Keywords

ADHD, neurofeedback, biofeedback, computer attention training

Brief summary

This study examines the efficacy of two computer-based attention training systems, one with and one without neurofeedback. The training systems intend to help children learn to focus and attend more effectively.

Detailed description

The current study is examining a neurofeedback (NF) computer attention training system that teaches children to alter their brainwave activity with a Cognitive Training attention training system (CT). The investigators hypothesize that both treatments will show improvement in ADHD symptoms and academic outcomes compared to a control condition. 104 children with ADHD in grades 2 and 4 are randomly assigned to receive the NF, CT, or a Waitlist-Control (WLC) condition that receives NF or CT the following academic year. Children receive forty 45-minute sessions three times a week at school for 4 months. A comprehensive assessment, consists of data completed by teachers, parents, participants, and double-blind classroom observations.

Interventions

BEHAVIORALNeurofeedback

3 times per week for 45 minutes for a total of 40 sessions

BEHAVIORALCognitive Training

3 times per week for 45 minutes for a total of 40 sessions

OTHERWaitlist Control

6 30 minute calm breathing sessions over the course of 4 months

Sponsors

Tufts Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Years to 12 Years
Healthy volunteers
Yes

Inclusion criteria

* diagnosis of ADHD (any subtype, per report of the child's physician or school psychologist) entering 2nd or 4th grade at the beginning of September 2009 and 2010. * combined IQ (Intelligence Quotient) at or above 80, * ability to read English sufficiently to complete assessments and intervention protocols

Exclusion criteria

* mental retardation, * coexisting diagnosis of conduct disorder, * pervasive developmental disorder, or * other serious mental illness (eg., bipolar disorder, psychosis, autism)

Design outcomes

Primary

MeasureTime frameDescription
Behavioral Observations of Students in School (BOSS)up to three yearsFor the purpose of this study, the BOSS is a double blind classroom observation. Each participant is observed by a trained researcher for 15 minutes three times over the course of two days at each assessment point (before the intervention, after the intervention, and at a 6-month follow up) and is evaluated in the areas of off task behaviors (motor, verbal, and passive) and on task behaviors (active and passive).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026