Attention Deficit/Hyperactivity Disorder Clinical Trial
Official title:
International Study to Predict Optimised Treatment Response to Short or Long Acting Methylphenidate in Children and Adolescents With Attention Deficit/Hyperactivity Disorder.
The aim of the iSPOT-A study is to:
1. identify brain, genetic and cognitive markers of Attention Deficit/Hyperactivity
Disorder, and
2. identify brain, genetic and cognitive markers that predict treatment response to
short-acting methylphenidate in children and adolescents diagnosed with Attention
Deficit/Hyperactivity Disorder.
This is a multi-center, open-label effectiveness trial to identify objective indicators of
treatment response in ADHD subjects (versus healthy controls) using cognitive and brain
function measures, brain structure and genetic measures in subjects diagnosed with ADHD.
At least 672 naïve and treatment experienced subjects with ADHD will be enrolled from
approximately 10 primary care centers. These patients are to be outpatients.
In addition, up to 672 healthy (non-ADHD) control subjects will be recruited who match the
enrolled ADHD subjects in race, age, gender and years of education.
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