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Clinical Trials/NCT02407496
NCT02407496
Completed
Not Applicable

Neurophysiological Attention Test (NAT) for Objective Assessment of Attention Deficit Hyperactivity Disorder (ADHD)

Think Now Incorporated1 site in 1 country80 target enrollmentJune 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Attention Deficit Hyperactivity Disorder (ADHD)
Sponsor
Think Now Incorporated
Enrollment
80
Locations
1
Primary Endpoint
NAT Slow Fluctuation Measure
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is develop a new assessment tool for Attention Deficit-Hyperactivity Disorder (ADHD) and to then test its validity (i.e. ability to discriminate between individuals with ADHD and healthy controls).

Detailed Description

The purpose of this study is to develop a novel approach and software for analyzing electroencephalography (EEG) data to identify biomarkers of ADHD. Then to test the ability of this assessment tool to differentiate between adults with ADHD and healthy controls by comparing the classification accuracy of the metrics from the new tool to the classification accuracy of existing behavioral tests for ADHD.

Registry
clinicaltrials.gov
Start Date
June 2014
End Date
September 2015
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Gregory Simpson, Ph.D.

Chief Scientific Officer

Think Now Incorporated

Eligibility Criteria

Inclusion Criteria

  • Specific inclusion criteria for ADHD are:
  • meet established DSM-5 criteria for ADHD predominately inattentive or combined subtype with clinically significant levels of impairment, diagnosed by structured clinical interview, the Mini International Neuropsychiatric Interview, and corroborating information
  • Clinical Global Impression-Severity (CGI-S) score ≥ 4 for ADHD
  • no lifetime history of DSM-5 bipolar disorder, psychotic disorder, pervasive developmental disorder, obsessive-compulsive disorder, substance abuse, or substance dependence (except nicotine) as assessed wit the MINI
  • able in the opinion of the investigator to complete all required study procedures.

Exclusion Criteria

  • Exclusion criteria for both groups are:
  • History of diagnosis of childhood disorder other than ADHD (e.g. autism, dyslexia)
  • history of any general medical condition likely to require chronic use of medication with identified CNS effects suspected to alter cognitive performance
  • history of seizure disorder, brain tumor, other major neurological disorder or head injury resulting in loss of consciousness
  • serious oxygen deprivation
  • current psychopathology requiring ongoing treatment with antipsychotic medications, mood stabilizers, benzodiazepines, or anticonvulsants
  • current untreated psychopathology which is rated to be primary in terms of severity (greater than ADHD severity)
  • current treatment with guanfacine.

Outcomes

Primary Outcomes

NAT Slow Fluctuation Measure

Time Frame: A single measurement is made for each individual at DAY 1 - the time of the brain wave test.

The NAT EEG test simultaneously generates 2 EEG values and 1 behavioral value that are used together as an assessment metric for ADHD. This is a one-time measure to assess its magnitude in ADHD vs Controls.

Study Sites (1)

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