ADHD Clinical Trial
— COMPLYOfficial title:
Treatment Adherence and Compliance in Children and Adolescents on ADHD Medication and Emotional Expression in Clinical Practice
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.
| Status | Completed |
| Enrollment | 518 |
| Est. completion date | June 2009 |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 6 Years to 17 Years |
| Eligibility |
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 |
Observational Model: Cohort, Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| Germany | 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. | Bad Homburg |
| Lead Sponsor | Collaborator |
|---|---|
| Eli Lilly and Company |
Germany,
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