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The FDA approved the 15- to 20-minute test based on a study of 275 patients who had attention or behavioral issues. Clinicians evaluated the patients using the NEBA Health System as well as standard diagnostic tools like behavioral questionnaires, IQ tests and physical exams. An independent group of researchers then reviewed the data and reached a consensus on whether each patient had ADHD or not. The study results showed that use of the NEBA System helped doctors make a more accurate diagnosis than using traditional methods alone.
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