Study Results
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View full resultsBasic Information
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COMPLETED
NA
85 participants
INTERVENTIONAL
2015-09-30
2017-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
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enhanced myADHDportal.com
Version of the myADHDportal.com web software enhanced with family-management support to enable parents to be active partners in optimizing and maintaining medication continuity for their child
enhanced myADHDportal.com
Version of the myADHDportal.com web software enhanced with family-management support to enable parents to be active partners in optimizing and maintaining medication continuity for their child
treatment as usual standard portal
Standard version of myADHDportal.com web software
treatment as usual standard portal
Standard version of myADHDportal.com web software
Interventions
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enhanced myADHDportal.com
Version of the myADHDportal.com web software enhanced with family-management support to enable parents to be active partners in optimizing and maintaining medication continuity for their child
treatment as usual standard portal
Standard version of myADHDportal.com web software
Eligibility Criteria
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Inclusion Criteria
1. their child receives ADHD care at one of the pediatric primary care practices that is partnering to conduct this trial
2. child being registered on myADHDportal.com to initiate child assessment of ADHD
3. child age 6-10 years
4. child must not have been previously treated with ADHD medication
5. child prescribed ADHD medication within 12 months of enrolling in the study
Exclusion Criteria
6 Years
10 Years
ALL
No
Sponsors
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National Institute of Mental Health (NIMH)
NIH
Children's Hospital Medical Center, Cincinnati
OTHER
Responsible Party
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Principal Investigators
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William Brinkman, MD, MEd, MSc
Role: PRINCIPAL_INVESTIGATOR
Cincinnati Children's
Locations
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William B Brinkman
Cincinnati, Ohio, United States
Countries
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Provided Documents
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Document Type: Study Protocol
Document Type: Statistical Analysis Plan
Other Identifiers
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