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Cognitive Behavioral Therapy for Treatment of Adult Attention Deficit Hyperactivity Disorder - Article


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Clinical Trial: Cognitive Behavioral Therapy for Treatment of Adult Attention Deficit Hyperactivity Disorder

This study is currently recruiting patients.

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)

Purpose

This study will determine the efficacy of cognitive behavioral therapy (CBT) in treating adults with attention deficit hyperactivity disorder (ADHD).
Condition Intervention
Attention Deficit Disorder with Hyperactivity
 Behavior: Cognitive Behavioral Therapy
 Behavior: Relaxation techniques and education about ADHD

MedlinePlus related topics:  Attention Deficit Disorder with Hyperactivity

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study

Official Title: Efficacy of CBT for Residual ADHD in Adults

Further Study Details: 
Primary Outcomes: ADHD symptoms
Expected Total Enrollment:  72

Study start: September 2004

ADHD, previously believed to be a disorder of childhood, affects as many as 5 percent of adults. Adults with ADHD are at high risk for academic and occupational underachievement, relationship difficulties, and reduced quality of life. This study will determine whether CBT is more effective than ADHD education and relaxation techniques in treating adults with ADHD.

Participants will be randomly assigned to receive 12 to 15 weekly sessions of either CBT or training in which they will learn relaxation techniques and receive detailed information about ADHD. Questionnaires will be used to assess participants'''' ADHD symptoms at study entry and at study completion.

Study hypothesis: CBT is a more efficacious treatment for adult ADHD than education and relaxation techniques.

Eligibility

Ages Eligible for Study:  18 Years   -   65 Years,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • Diagnosis of adult ADHD of at least mild clinical severity (CGI score of 3 or greater)
  • Stabile on medications for adult ADHD for at least 2 months -Between 18 and 65 years old -Be able to give informed consent and comply with study procedures

Exclusion Criteria:

  • Moderate to severe major depression, clinically signficant panic disorder (CGI for depression or panic greater than 4), bipolar disorder, organic mental disorders, psychotic disorders, or pervasive developmental disorders -Active suicidality (HAM-D suidicality item rater 3 or 4)
  • Current substance abuse or dependence
  • IQ less than 90
  • Suicide risk
  • Prior participation in cognitive behavioral therapy

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00118911

Patty A. Duran, BS      617-726-3679    pduran@partners.org
Susan Sprich, PhD      617-726-5991    ssprich@partners.org

Massachusetts
      Massachusetts General Hospital, Boston,  Massachusetts,  02114,  United States; Recruiting
Patty A. Duran, BS  617-726-3679    pduran@partners.org 
Susan Sprich, PhD  617-726-5991    ssprich@partners.org 

Study chairs or principal investigators

Steve A. Safren, PhD,  Principal Investigator,  Fenway Community Health   
Susan Sprich, PhD,  Study Director,  Partners Health Organization   

More Information

Study ID Numbers:  R01-MH069812; 2003-P-000523
Record last reviewed:  July 2005
Last Updated:  July 21, 2005
Record first received:  July 11, 2005
ClinicalTrials.gov Identifier:  NCT00118911
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-07-26


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November 28, 2009



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