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

American Academy of Pediatrics

Status

Withdrawn

Conditions

Attention Deficit-hyperactivity Disorder

Treatments

Behavioral: Clinical decision support for medication titration

Study type

Interventional

Funder types

Other

Identifiers

NCT01769300

UB5MC20286

Details and patient eligibility

About

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).

Full description

In this cluster (site)-randomized trial of clinical decision support for ADHD medication titration, clinicians caring for children with ADHD whose families are initiating stimulant medication at that practice will be followed.

Two groups will be compared; an intervention group, which will receive the intervention-the clinical decision support (CDS)--, and a control group, who will not receive CDS. Over a 6-month period, the CDS will support guideline-based medication titration to achieve optimal symptom control with minimal side effects. The study will track the care delivered to affected children by the practitioners and will assess the endpoints of symptom reduction and side effects. There will also be a sub-study within the larger study which will give the team a better understanding about the pros and cons of consenting parents over the phone.

Sex

All

Ages

5 to 12 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Practice Eligibility Criteria

Willing to offer the possibility of study enrollment to their patients who have ADHD
Willing to use the Vanderbilt Assessment Rating Scale to assess and potentially, to monitor ADHD for study subjects
Utilize Integrated Health Connect as a means to collect the Vanderbilt Assessment Rating Scale
Use point-of-care reports for subjects enrolled in the study.

Patient Eligibility Criteria

The child must be between the ages of 5-12 years old
The child must be starting stimulant medication for the first time
Parent must be able to speak and read English
The child must not be diagnosed with a current manic episode, a psychotic disorder, or a pervasive developmental disorder (e.g. autism, Asperger's, Rett's disorder)
The child must not have reported suicidality or have conduct disorder, per parent/guardian report