Low-dose vs. Normal-dose Psychostimulants on Executive Functions in Individuals With ADHD
Attention Deficit Hyperactivity Disorders
About this trial
This is an interventional treatment trial for Attention Deficit Hyperactivity Disorders focused on measuring Attention Deficit Hyperactivity Disorders, Executive Function, Methylphenidate, Psychostimulants, Adolescent, Child, Working Memory, Prefrontal Cortex, Attention, Cognitive Function, Inhibition
Eligibility Criteria
Inclusion Criteria:
- Between the chronological ages of 6 and 18 years
- Average to above-average IQ (Parental report of an IQ above 90; we will take their word for it)
- Meet DSM-V criteria for ADHD (Combined type or Inattentive type)
- Currently treated with and responding to oral Psychostimulants >= 20 mg/day and not on a "drug holiday"
- Stable on current Psychostimulant dose for at least 2 weeks
- Able to communicate (understand, speak, and write) in English without the aid of an interpreter
- Able to execute simple manual response (button-press) as required for our tasks
- The child and parent give assent and consent respectively for the child's participation in this study
Exclusion Criteria:
- Patients with significant prior or current medical conditions that could impact neuropsychological performance such as traumatic brain injury, hypoxia, or unstable diabetes.
- Have any medical condition that could markedly increase sympathetic nervous system activity (e.g. catecholamine-secreting neural tumor), or who are taking a medication on a daily basis (e.g. pseudoephedrine, oral steroids) that has sympathomimetic activity. Note: regular on-label use of inhalers for asthma (e.g., albuterol, steroidal) is permitted
- Taking any psychotropic medication other than on-label Psychostimulants specifically prescribed to treat ADHD
- Have a major, uncorrected sensory impairment (e.g. significant hearing impairment despite hearing aids)
- Lack sufficient English language skills to perform our tasks
- Are taking medications other than their specifically prescribed Psychostimulants that may affect cognitive skills
- Have a documented history of Dyslexia (this may skew results on our cognitive measures), Bipolar I or II, psychosis, Depression, Autism Spectrum Disorders, or Disruptive Mood Dysregulation Disorder
- Have a past history of any severe adverse reaction to lowering of Psychostiumlant dose
- Patient has been non-compliant with Psychostimulants or is on a "drug holiday"
- Parental report of an IQ below 90 (we will take their word for it)
Sites / Locations
- Developmental Cognitive Neuroscience Lab, Department of Psychiatry, University of British Columbia
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
No Intervention
Normal-dose Psychostimulant, Low-dose
Low-dose Psychostimulants, Normal-dose
No intervention, No intervention
Normal-dose: Dose participants are currently taking as part of their prescription (on more than or equals to 20 mg/day of Psychostimulants) Low-dose: Half the normal dose
Normal-dose: Dose participants are currently taking as part of their prescription (on more than or equals to 20 mg/day of Psychostimulants) Low-dose: Half the normal dose
This arm is completely no intervention, and is ONLY for healthy volunteers. We are testing healthy volunteers of the same age to give us an estimate of order effects to help us correct for better performance in the 2nd session due simply to taking the same tests twice (note: the tests are Version A and B).