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Effectiveness of Combined Medication Treatment for Aggression in Children With Attention Deficit With Hyperactivity Disorder (The SPICY Study)
This study is currently recruiting participants.
Verified by National Institute of Mental Health (NIMH), March 2009
First Received: November 19, 2008   Last Updated: September 18, 2009   History of Changes
Sponsor: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)
ClinicalTrials.gov Identifier: NCT00794625
  Purpose

This study will determine the advantages and disadvantages of adding one of two different types of drugs to stimulant treatment for reducing aggressive behavior in children with attention deficit with hyperactivity disorder (ADHD).


Condition Intervention Phase
Attention Deficit Disorder With Hyperactivity
Drug: Valproate
Drug: Risperidone
Drug: Placebo
Drug: Stimulant medication
Behavioral: Behavioral family counseling
Phase IV

Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Parallel Assignment, Safety/Efficacy Study
Official Title: Adjunctive Treatment With Divalproex or Risperidone for Aggression Refractory to Stimulant Monotherapy Among Children With ADHD

Resource links provided by NLM:


Further study details as provided by National Institute of Mental Health (NIMH):

Primary Outcome Measures:
  • Aggressive behavior [ Time Frame: Measured weekly for 11 to 16 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • ADHD symptoms [ Time Frame: Measured weekly for 11 to 16 weeks ] [ Designated as safety issue: No ]

Estimated Enrollment: 270
Study Start Date: November 2008
Estimated Study Completion Date: April 2013
Estimated Primary Completion Date: November 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental
During Phase 1, participants will receive a stimulant medication. If they do not respond to the stimulant, they will add valproate and behavioral family counseling to their treatment during Phase 2. If they do not respond to valproate, they will be switched to risperidone.
Drug: Valproate
Standard therapeutic doses of valproate, set according to valproic acid blood level, for 8 weeks
Drug: Risperidone
Standard therapeutic doses of risperidone for 8 weeks
Drug: Stimulant medication
Stimulant medication standard in the care of ADHD, such as methylphenidate or dextroamphetamine
Behavioral: Behavioral family counseling
Weekly behavioral counseling with a therapist
2: Experimental
During Phase 1, participants will receive a stimulant medication. If they do not respond to the stimulant, they will add risperidone and behavioral family counseling to their treatment during Phase 2. If they do not respond to risperidone, they will switch to valproate.
Drug: Valproate
Standard therapeutic doses of valproate, set according to valproic acid blood level, for 8 weeks
Drug: Risperidone
Standard therapeutic doses of risperidone for 8 weeks
Drug: Stimulant medication
Stimulant medication standard in the care of ADHD, such as methylphenidate or dextroamphetamine
Behavioral: Behavioral family counseling
Weekly behavioral counseling with a therapist
3: Placebo Comparator
During Phase 1, participants will receive a stimulant medication. If they do not respond to the stimulant, they will add placebo and behavioral family counseling to their treatment during Phase 2.
Drug: Placebo
An inactive substance at identical dosing to active treatments for 8 weeks
Drug: Stimulant medication
Stimulant medication standard in the care of ADHD, such as methylphenidate or dextroamphetamine
Behavioral: Behavioral family counseling
Weekly behavioral counseling with a therapist

Detailed Description:

Attention deficit with hyperactivity disorder (ADHD) is a common childhood mental disorder that affects 3% to 5% of all American children. Symptoms of ADHD commonly include inability to focus or exercise normal inhibition, and in some cases, aggressive behavior. Approximately 33% to 50% of children with ADHD develop oppositional defiant disorder (ODD), and about 20% to 40% develop a conduct disorder (CD). These disorders are characterized by defiant, belligerent, and otherwise aggressive behavior. Treatment for ADHD generally includes use of stimulant medications that decrease impulsivity and increase attentiveness, such as methylphenidate (Ritalin) or dextroamphetamine (Dexedrine), but these do not always affect aggression. To treat aggression in ADHD, many physicians prescribe additional medications, including the mood stabilizing medication valproate and the antipsychotic medication risperidone.

There is no clinical evidence proving that using multiple types of medications is safe and effective. This study will treat children with ADHD and aggression with a combination of stimulants and antipsychotic or mood stabilizing medications to determine whether the aggressive behaviors and ADHD symptoms are reduced without harmful side effects.

This study has two phases. During the first phase, which will last 3 to 6 weeks, participants will be treated with normal ADHD stimulant medications. During the second phase, those whose aggressive behavior is not effectively suppressed by stimulant medication alone will then be randomly assigned to also receive valproate, risperidone, or placebo for 8 weeks. After 8 weeks, children whose aggression persists will be switched from either valproate to risperidone or risperidone to valproate for another 8 weeks. Those on placebo will not switch medications. All participants will attend weekly monitoring visits for 11 to 16 weeks over the course of the study. At these visits, aggression levels and medication side effects will be assessed. Families will also meet with the researchers to discuss the child's progress and will attend behavioral counseling with a therapist.

  Eligibility

Ages Eligible for Study:   6 Years to 12 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Presence of ADHD
  • Presence of persistent, clinically significant aggression
  • Presence of ODD or CD

Exclusion Criteria:

  • Presence of psychosis
  • Presence of a major developmental disability
  • Presence of a major mood disorder
  • Contraindications to stimulant, valproate, or risperidone treatment
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00794625

Contacts
Contact: Joseph C. Blader, PhD, MSc 631-632-8317 joseph.blader@stonybrook.edu
Contact: Ashley E. Conway, BSc 631-632-8317 ashley.conway@stonybrook.edu

Locations
United States, New York
Stony Brook University Medical Center Recruiting
Stony Brook, New York, United States, 11794-8790
Contact: Ashley E. Conway, BSc     631-632-8317     ashley.conway@stonybrook.edu    
Contact: David Margulies, MD     (631) 632-3160     david.margulies@stonybrook.edu    
Principal Investigator: Joseph C. Blader, PhD, MSc            
North Shore - LIJ Health System, Zucker Hillside Hospital Recruiting
Glen Oaks, New York, United States, 11040
Contact: Nikki Katsiotas, BA     718-470-8868     nkatsiot@nshs.edu    
Contact: Alison Berest, MA     718-470-8362     aberest@lij.edu    
Principal Investigator: Vivian Kafantaris, MD            
United States, Texas
University of Texas Health Science Center at San Antonio Recruiting
San Antonio, Texas, United States, 78229
Contact: Candy Rhine     210-617-7070 ext 250     rhine@uthscsa.edu    
Contact: Maria Silva     (210) 614-7070, ext. 251     maria@cgcsanantonio.org    
Principal Investigator: Steven Pliszka, MD            
Sub-Investigator: W. Burleson Daviss, M.D.            
Sub-Investigator: Thomas L. Matthews, M.D.            
Sponsors and Collaborators
Investigators
Principal Investigator: Joseph C. Blader, PhD, MSc Stony Brook University School of Medicine, State University of New York
  More Information

No publications provided

Responsible Party: Stony Brook University, State University of New York ( Joseph C. Blader, PhD )
Study ID Numbers: R01 MH080050, DSIR 84-CTM
Study First Received: November 19, 2008
Last Updated: September 18, 2009
ClinicalTrials.gov Identifier: NCT00794625     History of Changes
Health Authority: United States: Federal Government

Keywords provided by National Institute of Mental Health (NIMH):
Attention-Deficit/Hyperactivity Disorder
Aggressive Behavior
Oppositional Defiant Disorder
Conduct Disorder

Additional relevant MeSH terms:
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs
Psychotropic Drugs
Valproic Acid
Signs and Symptoms
Serotonin Antagonists
Pathologic Processes
Attention Deficit Disorder with Hyperactivity
Mental Disorders
Therapeutic Uses
Mental Disorders Diagnosed in Childhood
Hyperkinesis
Aggression
Disease
Tranquilizing Agents
Nervous System Diseases
Risperidone
Attention Deficit and Disruptive Behavior Disorders
Central Nervous System Depressants
Dopamine Antagonists
Enzyme Inhibitors
Antipsychotic Agents
Antimanic Agents
Dyskinesias
Pharmacologic Actions
Behavioral Symptoms
Serotonin Agents
GABA Agents
Neurologic Manifestations

ClinicalTrials.gov processed this record on November 30, 2009