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Effectiveness of Combined Medication Treatment for Aggression in Children With Attention Deficit With Hyperactivity Disorder (The SPICY Study)

Primary Purpose

Attention Deficit Disorder With Hyperactivity

Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Valproate
Risperidone
Placebo
Stimulant medication
Behavioral family counseling
Sponsored by
Joseph Blader
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Attention Deficit Disorder With Hyperactivity focused on measuring Attention-Deficit/Hyperactivity Disorder, Aggressive Behavior, Oppositional Defiant Disorder, Conduct Disorder

Eligibility Criteria

6 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • North Shore - LIJ Health System, Zucker Hillside HospitalRecruiting
  • Stony Brook University Medical CenterRecruiting
  • University of Texas Health Science Center at San AntonioRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

1

2

3

Arm Description

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.

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.

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.

Outcomes

Primary Outcome Measures

Aggressive behavior

Secondary Outcome Measures

ADHD symptoms

Full Information

First Posted
November 19, 2008
Last Updated
July 13, 2012
Sponsor
Joseph Blader
Collaborators
University of Texas, Northwell Health
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1. Study Identification

Unique Protocol Identification Number
NCT00794625
Brief Title
Effectiveness of Combined Medication Treatment for Aggression in Children With Attention Deficit With Hyperactivity Disorder (The SPICY Study)
Official Title
Adjunctive Treatment With Divalproex or Risperidone for Aggression Refractory to Stimulant Monotherapy Among Children With ADHD
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Unknown status
Study Start Date
November 2008 (undefined)
Primary Completion Date
November 2012 (Anticipated)
Study Completion Date
April 2013 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Joseph Blader
Collaborators
University of Texas, Northwell Health

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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).
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Attention Deficit Disorder With Hyperactivity
Keywords
Attention-Deficit/Hyperactivity Disorder, Aggressive Behavior, Oppositional Defiant Disorder, Conduct Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
270 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
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.
Arm Title
2
Arm Type
Experimental
Arm Description
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.
Arm Title
3
Arm Type
Placebo Comparator
Arm Description
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.
Intervention Type
Drug
Intervention Name(s)
Valproate
Other Intervention Name(s)
Depakote, Valproic acid
Intervention Description
Standard therapeutic doses of valproate, set according to valproic acid blood level, for 8 weeks
Intervention Type
Drug
Intervention Name(s)
Risperidone
Other Intervention Name(s)
Risperdal
Intervention Description
Standard therapeutic doses of risperidone for 8 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Inactive substance, "Sugar pill"
Intervention Description
An inactive substance at identical dosing to active treatments for 8 weeks
Intervention Type
Drug
Intervention Name(s)
Stimulant medication
Other Intervention Name(s)
Ritalin, Dexedrine
Intervention Description
Stimulant medication standard in the care of ADHD, such as methylphenidate or dextroamphetamine
Intervention Type
Behavioral
Intervention Name(s)
Behavioral family counseling
Intervention Description
Weekly behavioral counseling with a therapist
Primary Outcome Measure Information:
Title
Aggressive behavior
Time Frame
Measured weekly for 11 to 16 weeks
Secondary Outcome Measure Information:
Title
ADHD symptoms
Time Frame
Measured weekly for 11 to 16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility 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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Joseph C. Blader, PhD, MSc
Phone
631-632-8317
Email
joseph.blader@stonybrook.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Lauren M. Chorney, PhD
Phone
631-632-8317
Email
lauren.chorney@stonybrook.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joseph C. Blader, PhD, MSc
Organizational Affiliation
Stony Brook University School of Medicine, State University of New York
Official's Role
Principal Investigator
Facility Information:
Facility Name
North Shore - LIJ Health System, Zucker Hillside Hospital
City
Glen Oaks
State/Province
New York
ZIP/Postal Code
11040
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ingrid S Fuentes, BA
Phone
718-470-8487
Email
isfuentes@nshs.edu
First Name & Middle Initial & Last Name & Degree
Allison Berest, BA
Phone
718-470-8868
Email
nkatsiot@nshs.edu
First Name & Middle Initial & Last Name & Degree
Vivian Kafantaris, MD
Facility Name
Stony Brook University Medical Center
City
Stony Brook
State/Province
New York
ZIP/Postal Code
11794-8790
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lauren M Chorney, PhD
Phone
631-632-8317
Email
lauren.chorney@stonybrook.edu
First Name & Middle Initial & Last Name & Degree
Gabrielle A Carlson, MD
Phone
(631) 632-8842
Email
gabrielle.carlson@stonybrook.edu
First Name & Middle Initial & Last Name & Degree
Joseph C. Blader, PhD, MSc
Facility Name
University of Texas Health Science Center at San Antonio
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Candy Rhine
Phone
210-614-7070
Ext
250
Email
rhine@uthscsa.edu
First Name & Middle Initial & Last Name & Degree
Maria Silva
Phone
(210) 614-7070
Ext
251
Email
maria@cgcsanantonio.org
First Name & Middle Initial & Last Name & Degree
Steven Pliszka, MD
First Name & Middle Initial & Last Name & Degree
Thomas L. Matthews, M.D.

12. IPD Sharing Statement

Citations:
PubMed Identifier
32007604
Citation
Blader JC, Pliszka SR, Kafantaris V, Foley CA, Carlson GA, Crowell JA, Bailey BY, Sauder C, Daviss WB, Sinha C, Matthews TL, Margulies DM. Stepped Treatment for Attention-Deficit/Hyperactivity Disorder and Aggressive Behavior: A Randomized, Controlled Trial of Adjunctive Risperidone, Divalproex Sodium, or Placebo After Stimulant Medication Optimization. J Am Acad Child Adolesc Psychiatry. 2021 Feb;60(2):236-251. doi: 10.1016/j.jaac.2019.12.009. Epub 2020 Jan 30.
Results Reference
derived
PubMed Identifier
26745211
Citation
Blader JC, Pliszka SR, Kafantaris V, Sauder C, Posner J, Foley CA, Carlson GA, Crowell JA, Margulies DM. Prevalence and Treatment Outcomes of Persistent Negative Mood Among Children with Attention-Deficit/Hyperactivity Disorder and Aggressive Behavior. J Child Adolesc Psychopharmacol. 2016 Mar;26(2):164-73. doi: 10.1089/cap.2015.0112. Epub 2016 Jan 8.
Results Reference
derived
PubMed Identifier
24290461
Citation
Blader JC, Pliszka SR, Kafantaris V, Foley CA, Crowell JA, Carlson GA, Sauder CL, Margulies DM, Sinha C, Sverd J, Matthews TL, Bailey BY, Daviss WB. Callous-unemotional traits, proactive aggression, and treatment outcomes of aggressive children with attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry. 2013 Dec;52(12):1281-93. doi: 10.1016/j.jaac.2013.08.024. Epub 2013 Sep 25.
Results Reference
derived

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Effectiveness of Combined Medication Treatment for Aggression in Children With Attention Deficit With Hyperactivity Disorder (The SPICY Study)

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