Improving Attention Deficit Hyperactivity Disorder Treatment Adherence and Outcome in Primary Care Settings
Improving Medication Use for ADHD in Primary Care
2 other identifiers
interventional
270
1 country
1
Brief Summary
This study will determine the effectiveness of educating pediatricians about attention deficit hyperactivity disorder treatment guidelines in improving child behavior and pediatricians' adherence to medication guidelines.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jun 2003
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2003
CompletedFirst Submitted
Initial submission to the registry
September 12, 2005
CompletedFirst Posted
Study publicly available on registry
September 16, 2005
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2009
CompletedAugust 17, 2015
August 1, 2015
6.1 years
September 12, 2005
August 14, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Behavior changes as rated by teachers
Measured at Month 12
Secondary Outcomes (3)
Behavior change as rated by parents
Measured at Month 12
Behavior changes as rated by classroom observation
Measured at Month 12
Relation between adherence to protocol and behavior change
Measured at Month 12
Study Arms (2)
1 Physician training
EXPERIMENTALPhysician participants will receive training in guidelines and medication monitoring
2
NO INTERVENTIONPhysician participants will provide usual care and no special intervention
Interventions
Physicians are trained in guidelines for medication management.
Eligibility Criteria
You may qualify if:
- Presence of ADHD
- Not currently on medication
You may not qualify if:
- No serious neurological disorders of sever mental health problems (suicidal behavior, autism)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ann & Robert H Lurie Children's Hospital of Chicago
Chicago, Illinois, 60611, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
John V. Lavigne, PhD
Ann & Robert H Lurie Children's Hospital of Chicago
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Chief Psychologist
Study Record Dates
First Submitted
September 12, 2005
First Posted
September 16, 2005
Study Start
June 1, 2003
Primary Completion
July 1, 2009
Study Completion
July 1, 2009
Last Updated
August 17, 2015
Record last verified: 2015-08