Treatment Adherence and Compliance in Children and Adolescents on ADHD Medication and Emotional Expression in Clinical Practice
Overview
- Phase
- Not Applicable
- Intervention
- Atomoxetine
- Conditions
- ADHD
- Sponsor
- Eli Lilly and Company
- Enrollment
- 518
- Locations
- 1
- Status
- Completed
- Last Updated
- 16 years ago
Overview
Brief Summary
The primary research objective of this observational study is to evaluate treatment compliance over one year in children and adolescents who are newly initiated on medication approved for the treatment of ADHD in a routine clinical setting. Compliance will be assessed using the Pediatric Compliance Self-Rating (PCSR) Instrument. A patient will be considered as compliant at a given visit, if the PCSR score is at least 5, corresponding to taking the medication at least often.
Investigators
Eligibility Criteria
Inclusion Criteria
- •6-17 years old
- •diagnosis of ADHD according to ICD-10 or DSM-IV criteria
- •new initiation onto an approved medication to treat ADHD
Exclusion Criteria
- •no specific exclusion criteria
Arms & Interventions
A
A: ADHD-patients receiving non-stimulants (e.g. atomoxetine)
Intervention: Atomoxetine
B
B: ADHD-patients receiving stimulants
Intervention: stimulants (any approved ADHD medication)
Outcomes
Primary Outcomes
Not specified