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Clinical Trials/NCT00071656
NCT00071656
Completed
N/A

Psychosocial Treatment for ADHD Inattentive Type I

University of California, San Francisco1 site in 1 country60 target enrollmentSeptember 2002

Overview

Phase
N/A
Intervention
Not specified
Conditions
Attention Deficit Disorder With Hyperactivity
Sponsor
University of California, San Francisco
Enrollment
60
Locations
1
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The purpose of this study is to develop and implement a treatment that focuses on behaviors to reduce symptom severity and functional impairment in patients with Attention Deficit Hyperactivity Disorder, Predominantly Inattentive Type (ADHD-I). The long-term goal of this study is to apply the treatment to larger-scale trials to determine its effectiveness and generalizability.

Detailed Description

ADHD-I is a highly prevalent and serious childhood disorder that affects academic and social development. The symptoms of ADHD-I differ from those of the well-studied ADHD Combined Type. Unfortunately, studies of psychosocial interventions for ADHD-I are currently unavailable. Effective treatments for ADHD-I are still needed. Participants are randomly assigned to receive either a behavioral intervention or treatment as usual for 10 to 12 weeks. The behavioral intervention includes parent and child skill development groups, family meetings, and consultation with the child's teacher to address attention problems and areas of impairment at home and school. Parent and child interviews, teacher and child ratings, and psychoeducational testing are used to assess participants. Participants are assessed post-treatment and at a 2-month follow-up visit.

Registry
clinicaltrials.gov
Start Date
September 2002
End Date
June 2007
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • ADHD, Predominantly Inattentive Type
  • Public or private school attendance
  • English speaking

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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