Methylphenidate for Treating Children With ADHD and Tourette Syndrome

Sponsor
Stony Brook University (Other)
Overall Status
Completed
CT.gov ID
NCT00441649
Collaborator
National Institute of Mental Health (NIMH) (NIH)
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Study Details

Study Description

Brief Summary

This study will evaluate the safety and effectiveness of methylphenidate in treating attention deficit hyperactivity disorder in children with both attention deficit hyperactivity disorder and Tourette syndrome.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

Tourette syndrome is a neurological disorder that is characterized by repetitive, involuntary movements and vocalizations called tics. Many children with Tourette syndrome also have attention deficit hyperactivity disorder (ADHD), which is one of the most common childhood mental disorders. Symptoms of ADHD usually include impulsiveness, inattention, and hyperactivity. ADHD is commonly treated with a stimulant medication, such as methylphenidate. It is under debate, however, whether using stimulants in children with Tourette syndrome exacerbates tics associated with the disorder. This study will evaluate the safety and effectiveness of methylphenidate in treating ADHD in children who have both ADHD and Tourette syndrome.

Participants in this 6-week, double blind study will receive three doses of methylphenidate over the course of the study. Each dose will be taken twice daily, approximately 3.5 hours apart, for 2 weeks. Medication will be dispensed at study visits, which will occur once every 2 weeks. At each study visit, participants will take a dose of the medication. About an hour after ingesting the medication, they will be observed in a classroom setting by study physicians. Participants will then complete a Continuous Performance Test, which will measure their voluntary attention levels. The following will be assessed at study visits: ADHD symptoms; oppositional and aggressive behavior; frequency and severity of tics and obsessive compulsive disorder symptoms; rebound tic exacerbation; effects of methylphenidate on tic-related problems with self-esteem, family life, academic and social performance, and overall tic severity; anxiety and mood symptoms; and adverse drug reactions. Parents and teachers will also complete assessments of participants' behavior on 2 days of each week for the duration of the study.

Study Design

Study Type:
Interventional
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
Double
Primary Purpose:
Treatment
Official Title:
Methylphenidate Treatment of ADHD in Children With Tourette Syndrome
Study Start Date :
Feb 1, 2000
Actual Primary Completion Date :
Jun 1, 2004
Actual Study Completion Date :
Jan 1, 2007

Outcome Measures

Primary Outcome Measures

  1. ADHD symptoms []

  2. Oppositional and aggressive behavior []

  3. Frequency and severity of tics and obsessive compulsive disorder symptoms []

  4. Tic impairment, tic severity, and clinical response []

  5. Anxiety and mood symptoms []

  6. Rebound tic exacerbation []

  7. Adverse drug reactions (all measured at 2-week intervals throughout the study) []

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years to 12 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Diagnosis of ADHD or ADHD plus Tourette syndrome
Exclusion Criteria:
  • Determined to be dangerous to self or others

  • Scores less than 70 on an IQ test

  • Any seizure disorder, major organic brain dysfunction, major medical illness, major mood disorder, psychosis, pervasive developmental disorder, or peripheral sensory loss

  • Any condition that may make use of methylphenidate unsafe

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Stony Brook University
  • National Institute of Mental Health (NIMH)

Investigators

  • Principal Investigator: Kenneth D. Gadow, PhD, State University of New York at Stony Brook

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00441649
Other Study ID Numbers:
  • R01MH045358
  • R01MH045358
  • DDTR B2-NDH
First Posted:
Mar 1, 2007
Last Update Posted:
Oct 31, 2013
Last Verified:
Oct 1, 2013
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 31, 2013