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N/A N=302

Adult Normative Performance of the Quotient ADHD System

ADHD

Enrolled (actual)
302
Serious AEs
0.0%
Results posted
Oct 2013
Primary outcome: Primary: Well-screened, Non-ADHD Controls to Augment the Existing Adolescent and Adult Database Thus Expanding the Normative Reference Range of Performance of the Quotient® Adolescent and Adult Version Test. — 300 participants

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Pediatric, Adult · 15+ yrs
Sex
All
Sponsor
BioBehavioral Diagnostics Company
Primary completion
Jun 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Well-screened, Non-ADHD Controls to Augment the Existing Adolescent and Adult Database Thus Expanding the Normative Reference Range of Performance of the Quotient® Adolescent and Adult Version Test.
300

Summary

This study is being conducted to enhance and extend the clinical utility of the Quotient® ADHD System Adolescent and Adult Version Test by adding large numbers of well-screened controls to the existing Quotient® ADHD System database of adolescents and adults (ages 15-55).

Eligibility Criteria

Inclusion Criteria

Subjects are eligible for enrollment if they fulfill the following inclusion criteria:

  • Male or Female
  • Ages 15 to 55
  • Un-medicated with medications known to affect ADHD or cognitive functioning
  • Report of good physical health
  • Able to understand test instructions and comply with testing
  • Willing to give written informed consent and/or assent

Exclusion Criteria

  • History of diagnosis of ADHD
  • History of known neurological disease or insult (e.g., head trauma with LOC, skull fracture, past or present migraine headaches, seizure disorders)
  • Major Medical Disorders
  • Past/present alcohol or substance abuse or dependence
  • Current or past DSM-IV disorder, screened by the computerized SCID I & II, and reviewed by investigator
  • Any major medical or neurological condition that could affect motor activity or attention (e.g. Parkinson's, MS, dementia)
  • Currently ill with cold/flu/infections which may compromise their ability to perform the computer task
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01308450). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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