Improving the Medication Management of Patients With Attention-Deficit Hyperactivity Disorder

Withdrawn before enrolling · Not applicable

Conditions studied: Attention Deficit-hyperactivity Disorder

In brief

The specific aim of this cluster-randomized (site) comparative effectiveness research study is to determine whether children who are (1) 5-12 years of age, (2) cared for in ePROS practices or clinics using an electronic health record (EHR), (3) have attention-deficit hyperactivity disorder (ADHD), and (4) are to receive treatment with stimulant medication for the first time in these practices, have superior clinical outcomes if their clinicians have access to an EHR-guided clinical decision support system (intervention group) than if their clinicians have no such access (control group).

Key facts

Study ID
NCT01769300
Run by
American Academy of Pediatrics
People needed
0
Starts
2013-01-01
Expected to finish
2014-08-01
Last updated by the study team
2018-07-13

Who can join

Age: 5 and older, up to 12. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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