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Clinical Trials/NCT01487967
NCT01487967
Completed
N/A

Preference and Goal-Directed Primary Care to Minimize Disparities and Improve Outcomes in ADHD

Children's Hospital of Philadelphia1 site in 1 country120 target enrollmentJanuary 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Attention Deficit Hyperactivity Disorder
Sponsor
Children's Hospital of Philadelphia
Enrollment
120
Locations
1
Primary Endpoint
Feasibility of family recruitment and follow-up
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This pilot intervention study will test the feasibility and acceptability and explore the outcomes of an urban, primary care-based intervention to measure families' preferences and goals for Attention-Deficit/Hyperactivity Disorder (ADHD) treatment and structure clinical care to reach these goals.

Detailed Description

The intervention includes provision of enhanced, culturally appropriate education about ADHD and its treatment, completion of a validated preference and goal instrument, use of this instrument in the ADHD treatment decision-making process, and tracking of preferences and goals over time.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
June 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All interested non-trainee clinicians at study sites
  • Parents/legal guardians of children age 6-12, in K-6 grade, diagnosed with ADHD.

Exclusion Criteria

  • child diagnosed with autism or a psychotic disorder
  • parents non-English speaking
  • parents unable to provide consent
  • pediatric residents

Outcomes

Primary Outcomes

Feasibility of family recruitment and follow-up

Time Frame: Up to 24 months

The feasibility of this intervention will be assessed by examining the proportion of families screened that meet enrollment criteria, the proportion meeting enrollment criteria that enroll, and the proportion enrolled that complete each study measure.

Secondary Outcomes

  • Parent Engagement(Up to 24 months)
  • Clinical Outcomes(Baseline, after 3 months, after 6 months)
  • Acceptability of the intervention to parents and clinicians(Up to 24 months)
  • Joint Participation in Decision-Making and Partnership(Baseline)
  • Treatment Acceptability(Baseline, after 3 months, after 6 months)
  • Treatment Adherence/Receipt(Up to 24 months)
  • Goal Attainment(after 3 months, after 6 months)

Study Sites (1)

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