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Effectiveness of a Electroencephalogram (EEG) Biofeedback for the Treatment of ADHD

Pilot Trial of a Brain-computer Interface System Based Programme for the Treatment of ADHD

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00802490
Acronym
EEG
Enrollment
20
Registered
2008-12-05
Start date
2008-05-31
Completion date
2012-06-30
Last updated
2013-02-22

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

Attention Deficit Hyperactivity Disorder, Electroencephalogram biofeedback, Inattention, Brain-Computer Interface System

Brief summary

The aim of this study is to investigate if electroencephalogram (EEG) biofeedback incorporating the use of video games is effective in improving inattentive symptoms in children with ADHD.

Detailed description

This study will enroll 20 outpatient subjects aged 7 to 12 newly diagnosed with ADHD who have never received treatment with medication. These children should have inattentive symptoms, i.e. diagnosed with combined or inattentive subtype of ADHD, and should not have any of the exclusion criteria. Based on the gender ratios from other studies, we will enroll 8 boys and 2 girls into the intervention group, giving a male:female ratio of 4:1. 10 will be in the 'intervention' group and 10 in the 'control' group. Informed consent will be obtained from the parents, and assent from the subjects, prior to any form of assessment or intervention as part of the study. INTERVENTION The 10 subjects in the intervention group will take part in a total of 20 sessions spread over a 10-week period. Each subject will first need to master a simple concentration task involving a fishing game. After this, the child will go on to play a second soccer game. Each game employs the BCI system, and is controlled by the child's concentration, which is fed to the computer via the EEG leads. The child watches the game on a computer screen. Each session may take approximately thirty minutes. The other 10 children in the comparison group will act as controls. At the clinic visit at baseline assessment, they will play the fishing game. There will be no further intervention subsequently. ASSESSMENT The following questionnaires will be administered to all subjects in both study groups at week 5, week 10, and at 3 months post-intervention (week 22): 1. ADHD Rating Scale: parents and teachers 2. Child Behaviour Checklist (CBCL): parents 3. Teacher's Report Form (TRF): teachers In addition, for those subjects in the intervention group, they will be given 2 worksheets (1 Maths and 1 short comprehension exercise) at the end of the intervention during visits 2, 4, 6, 8, 10, 12, 14, 16, 18 and 20 over the 10-week period. Their EEG activity will be recorded during the completion of these worksheets.

Interventions

DEVICEBrain-Computer Interface System

Newly-developed video games employing neurofeedback strategy to be played twice a week, 1 hour per session for a period of ten weeks.

Sponsors

Institute for Infocomm Research
CollaboratorOTHER
Duke-NUS Graduate Medical School
CollaboratorOTHER
National Healthcare Group, Singapore
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
7 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Satisfy DSM-IV-TR criteria for ADHD (Combined OR Inattentive subtype)

Exclusion criteria

* Present or history of medical treatment with stimulant medication and/or Atomoxetine * Co-morbid severe psychiatric condition or known sensori-neural deficit, e.g. complete blindness or deafness * History of epileptic seizures * Known mental retardation (i.e. IQ 70 and below) * Predominantly hyperactive/impulsive subtype of ADHD

Design outcomes

Primary

MeasureTime frame
Reliable Change Index (RCI)on ADHD Rating Scaleweek 0, 5, 10, 22

Secondary

MeasureTime frame
CBCL Attention Problem Score ChangeWeek 5, 10, 22

Countries

Singapore

Outcome results

None listed

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