The purpose of this study is to assess whether changes in the symptoms of ADHD show a relationship with changes in functioning in children with ADHD treated with atomoxetine over a 3-month period.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
200
To assess the correlation of change in score on an ADHD rating scale with the change in score on a functional rating questionnaire at 3 months post atomoxetine initiation
Understand the relationships between ADHD symptoms, functional outcomes, and quality of life
Explore the impact of data collection time points on efficacy, quality of life, and functional outcome
Assess the efficacy of atomoxetine
Use data collected to validate the WFIRS-P questionnaire
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Calgary, Alberta, Canada
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Edmonton, Alberta, Canada
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Abbotsford British Columbia, British Columbia, Canada
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Burnaby, British Columbia, Canada
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Kelowna, British Columbia, Canada
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Langley, British Columbia, Canada
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Vancouver, British Columbia, Canada
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Winnipeg, Manitoba, Canada
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Moncton, New Brunswick, Canada
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Saint John, New Brunswick, Canada
...and 9 more locations