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Clinical Trials/NCT01118650
NCT01118650WithdrawnNot Applicable

Concordance of the Quotient ADHD System Report With Teacher and Parent Assessments in School-Aged Children Receiving an Individualized Education Program (IEP) or 504 Accommodations in the Classroom Setting for Symptoms of Attention-Deficit/Hyperactivity Disorder (ADHD)

BioBehavioral Diagnostics Company0 sitesStarted: June 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Sponsor

Study Overview

Brief Summary

To demonstrate concordance between the Quotient ADHD System Report and standard DSM-IV based parent and teacher reported rating/assessment scales, currently the accepted method of symptom measurement for subjects diagnosed with Attention-Deficit/Hyperactivity Disorder (ADHD).

Detailed Description

Public school based study for children ages 8 through 14 years of age.

Children previously identified and currently receiving an Individualized Education Program (IEP) or 504 accommodations in the classroom setting for symptoms of ADHD.

Open enrollment of 30 subjects, both male and female.

One study visit in which subjects will perform/receive the following assessments/evaluations:

  1. Quotient ADHD System Test
  2. Vanderbilt ADHD Diagnostic Teacher Rating Scale
  3. Vanderbilt ADHD Diagnostic Parent Rating Scale

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
8 Years to 14 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • A student attending one of three public elementary schools in the New Hampshire School Administrative Unit #
  • Age 8 through 14 years old at time of enrollment.
  • Pre-identified as receiving an Individualized Education Program (IEP) or 504 accommodations for symptoms of ADHD in the school setting by the Special Education Coordinator in the school district.
  • A parent/guardian of the child must be willing to participate.

Exclusion Criteria

  • No subject will be excluded from participation based on race, ethnicity, or gender. Anyone meeting inclusion criteria, who are willing to sign consent and participate, will be included in the study.

Investigators

Sponsor
BioBehavioral Diagnostics Company
Sponsor Class
Industry
Responsible Party
Sponsor

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