Clinical Trials Directory

Trials / Terminated

TerminatedNCT03523663

System for Determining Ideal Drug Doses for ADHD - Stages 1 and 2

Algorithm to Quantitatively Determine the Ideal Drug Dose to Treat Attention Deficit Hyperactivity Disorder

Status
Terminated
Phase
Study type
Observational
Enrollment
46 (actual)
Sponsor
University of Wisconsin, Madison · Academic / Other
Sex
All
Age
8 Years – 12 Years
Healthy volunteers
Accepted

Summary

The goal of this study is to create a formal, quantitative methodology to determine what is the most beneficial dose of Central Nervous System (CNS) stimulant (Ritalin, methylphenidate) to improve cognitive and behavioral function of children diagnosed with Attention Deficit Hyperactivity Disorder (ADHD) individually. If successful, it will change the way in which the dose of CNS stimulant for treating ADHD is determined for children in need of therapeutic intervention. The project will be focused on developing the necessary methodology to analyze the children's data with the drift-decision model (DDM), and to develop the required technology, i.e., a computer game with which to measure cognitive/behavioral function and its validation with eye-tracking measurements.

Conditions

Interventions

TypeNameDescription
OTHERno intervention. measure eye movement data

Timeline

Start date
2016-01-01
Primary completion
2019-09-11
Completion
2019-09-11
First posted
2018-05-14
Last updated
2021-12-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03523663. Inclusion in this directory is not an endorsement.