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Clinical Trials/NCT00540826
NCT00540826
Completed
Not Applicable

Treatment Adherence and Compliance in Children and Adolescents on ADHD Medication and Emotional Expression in Clinical Practice

Eli Lilly and Company1 site in 1 country518 target enrollmentNovember 2007

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.

Registry
clinicaltrials.gov
Start Date
November 2007
End Date
June 2009
Last Updated
16 years ago
Study Type
Observational
Sex
All

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

Study Sites (1)

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