Treatment of Youth With ADHD and Anxiety
Information source: National Institute of Mental Health (NIMH)
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Attention Deficit Hyperactivity Disorder; Anxiety, Separation; Social Phobia; Generalized Anxiety Disorder
Intervention: methylphenidate (Drug); fluvoxamine (Drug)
Phase: N/A
Status: Completed
Sponsored by: National Institute of Mental Health (NIMH)
Summary
The purpose of this NIMH-sponsored pilot study is to collect information on the efficacy and
safety of drug treatments for children and adolescents who suffer from both ADHD and anxiety
disorders. Specifically, the study will examine the benefits of the stimulant medication both
alone and in combination with fluvoxamine, a selective serotonin reuptake inhibitor (SSRI)
that has antianxiety effects. Young people aged 6 to 17 diagnosed with these co-occurring
disorders may be eligible to participate.
Clinical Details
Official title: A Treatment Study of Youth With Comorbid Attention Deficit Hyperactivity Disorder (ADHD) and Anxiety Disorders
Study design: Treatment, Randomized, Open Label, Uncontrolled, Crossover Assignment, Safety/Efficacy Study
Detailed description:
Many children and adolescents with mental disorders in the United States are treated with
multiple psychotropic medications even though there is not much information on how well these
medications work together or if they are safe to administer together. Many youth with ADHD
have co-occurring (comorbid) disorders such as oppositional-defiant disorder, anxiety
disorders, and mood disorders. There is much interest in the treatment of children and
adolescents with comorbid ADHD and anxiety disorders because this is a common condition in
clinical practice. When children with both anxiety and ADHD receive stimulant medication for
ADHD, their anxiety may not improve. SSRI medications represent a reasonable addition to
stimulant treatment, as they are considered effective for anxiety disorders based on
controlled trials in adults and open trials in children. However, there are no data from
controlled studies regarding the tolerability and dosing of the combination of stimulant
treatment (including methylphenidate) and SSRIs in the treatment of children with comorbid
ADHD and anxiety disorder.
In this study, children and adolescents will be evaluated for the presence of both ADHD and
Anxiety Disorder. Approximately 120 children and adolescents with both disorders who meet all
the study entry requirements (such as being otherwise medically healthy) will be enrolled.
Children and adolescents who are not on a stable dose of a stimulant will first be treated
openly with methylphenidate for 6 weeks. Those whose ADHD does not improve during this
initial treatment period will not continue in the study but will be referred for further
support in the community. Those who show improvement in both their ADHD and anxiety symptoms
will stay on methylphenidate for an additional 8 weeks. Those who show improvement in ADHD
but not anxiety will be asked to enter the double-blind phase of the study. In this phase,
participants will be randomized (assigned by chance) to receive either fluvoxamine or
placebo, in combination with stimulant/methylphenidate, for 8 weeks. Children or adolescents
who enter the study on a stable dose of stimulant will move directly to the Double-Blind
phase. Participants who are assigned to placebo and who do not show an improvement in anxiety
after 8 weeks will be eligible for an additional 8 weeks of open treatment with the
methylphenidate/stimulant and fluvoxamine combination. At the end of the trial, clinical
care will be provided for up to an additional month until referral to an outside clinician
can be arranged.
Eligibility
Minimum age: 6 Years.
Maximum age: 17 Years.
Gender(s): Both.
Criteria:
- ADHD diagnosis
- DSM-IV diagnosis of anxiety
- IQ greater than 70
- residence with primary caretaker for at least 6 months
- ages 6-17 and attending school
- no previous treatment failure to or intolerance of fluvoxamine or methylphenidate
(unless currently taking another stimulant)
Locations and Contacts
UCLA Neuropsychiatric Institute, Los Angeles, California 90095, United States
Johns Hopkins School of Medicine, Baltimore, Maryland 21287, United States
New York State Psychiatric Institute, New York, New York 10032, United States
New York University Child Study Center, New York, New York 10016, United States
Duke University Medical Center, Durham, North Carolina 27710, United States
Additional Information
More information on ADHD More information on anxiety
Related publications: [No authors listed] Fluvoxamine for the treatment of anxiety disorders in children and adolescents. The Research Unit on Pediatric Psychopharmacology Anxiety Study Group. N Engl J Med. 2001 Apr 26;344(17):1279-85. Coyle JT. Drug treatment of anxiety disorders in children. N Engl J Med. 2001 Apr 26;344(17):1326-7. No abstract available.
Starting date: November 2000
Ending date: May 2002
Last updated: February 8, 2008
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