Study to Determine Whether There Are Any Cognitive or Motor Effects From Taking the Medicine Risperidone.
Primary Purpose
Oppositional Defiant Disorder, Conduct Disorder, Attention Deficit/Hyperactivity Disorder (ADHD)
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Risperdal
Sponsored by
About this trial
This is an interventional diagnostic trial for Oppositional Defiant Disorder focused on measuring Severe conduct problems, Risperidone, Risperdal
Eligibility Criteria
Inclusion Criteria:
- Aged 4 to 14 years, inclusive
- Male or female gender
- Reason for receiving risperidone must include severe conduct problems
- Received risperidone treatment for at least 4 months
- Dosage in the range of 0.01 to 0.099 mg/kg/day
- Capable of discontinuing risperidone for up to 14 days in the judgement of child's physician
- Taking co-therapy with psychostimulants, antihistamines, melatonin, and chloral hydrate is allowed as long as co-therapy is held constant
- Taking co-therapy for sleep with guanfacine hydrochloride, clonidine hydrochloride, and trazodone hydrochloride is allowed so long as co-therapy is held constant
- Must have a reliable adult carer who can report on subject's behavior and attend scheduled assessments
- Parent or guardian must give informed consent, and subject must give assent if 14 years of age or older
- Must be considered physically healthy on the basis of physical exam and medical history.
Exclusion Criteria:
- Patients who meet DSM-IV criteria for schizophrenia, schizophreniform disorder, dissociative disorder, major depression, schizoaffective disorder, substance induced psychotic disorder
- Subjects who are pregnant
- Subjects with known seizure disorder
- Subjects with a history of neuroleptic malignant syndrome
- Subjects with a known or suspected history of severe drug allergy or hypersensitivity
- Subjects must have no significant medical disease
- Subjects must not be taking any other psychotropic medications.
Sites / Locations
- Ohio State University Nisonger Center
Outcomes
Primary Outcome Measures
Short Term Recognition Memory task (accuracy)
Titrated Delayed Matching-to-Sample task (accuracy)
Continuous Performance task (omission errors)
Seat Activity
Graduated Holes task (errors and error times)
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00399698
Brief Title
Study to Determine Whether There Are Any Cognitive or Motor Effects From Taking the Medicine Risperidone.
Official Title
Effects of Risperidone on Cognitive-Motor Performance and Motor Movements in Chronically Medicated Children
Study Type
Interventional
2. Study Status
Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
May 1999 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2005 (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University
4. Oversight
5. Study Description
Brief Summary
This study was developed in order to assess the effects of risperidone (Risperdal) as compared with placebo on cognitive-motor performance (attention, memory, and hand steadiness) and body movements.
We propose to study the effects of risperidone on cognitive-motor performance in children already medicated for severe conduct problems. We would also like to look at safety by assessing these children for dyskinetic movements. We already have a sizable cohort of children maintained on risperidone. Our hypotheses are as follows:
Risperidone will have no adverse effects on cognitive-motor performance in children who have received maintenance therapy for 4 to 20 months.
Children tested during placebo will show no more dyskinetic movements than during risperidone treatment (i.e., there will be no unmasking of tardive dyskinesia).
Detailed Description
Antipsychotics are fairly commonly used for managing certain psychiatric disorders that occur in childhood: schizophrenia, autistic disorder, delusional manic depressive disorder, bipolar disorder, conduct disorder, and disruptive behavior associated with mental retardation (Botteron & Geller, 1998). They are also occasionally used for ADHD when more conventional treatments, such as psychostimulants and tricyclic antidepressants, have failed (Botteron & Geller, 1998). Despite a helpful role for the antipsychotic medications in many childhood conditions, there is a persistent although poorly substantiated impression that these medicines cause "cognitive blunting" in children. This may be more commonly heard than seen in print, but we believe that it is the cause of considerable resistance to antipsychotic treatment by physicians and nonmedical professionals alike.
At the same time, the data supporting the notion of cognitive blunting by antipsychotic medicines is largely negative (although limited in amount) and frequently badly out of date (see Ernst, Malone, Rowan, George, Gonzales, & Silva, 1998; Aman, 1984; Aman, Marks, Turbott, Wilsher, & Merry, 1991). There are good theoretical reasons to believe that novel antipsychotics may have no effects on cognition or may actually enhance cognitive functioning, at least in some disorders (Borison, 1996; Meltzer, 1995; Stip, 1996). At least one study thus far has shown significantly improved cognitive performance in schizophrenic patients taking risperidone as compared with such patients taking high-potency classical antipsychotics or no treatment (Gallhofer, Bauer, Lis, Krieger, & Gruppe, 1996).
Another source of resistance to the use of antipsychotic medicines with young people is the possibility that they may cause tardive dyskinesia. However, available data on the novel antipsychotics suggests that they are substantially safer than classical antipsychotics in this respect. Nevertheless, data are limited because of the newness of agents like risperidone.
Our laboratory at O.S.U. is unique because it has a sophisticated computer-controlled cognitive-motor test battery. O.S.U. is one of seven universities supported by NIMH as part of its network of Research Units on Pediatric Psychopharmacology ("RUPPs"). Recently, Dr. Mike Aman reviewed the available cognitive test systems on behalf of the Autism RUPP Group. From this exercise, it became quite clear to us that we maintain what is probably the world's best system for assessing the cognitive-motor effects of psychotropic drugs in children, especially children with developmental handicaps.
The experimental (research) portion of the treatment is to assess the effects of risperidone (Risperdal) on learning performance and motor movements in children. This study is looking at whether or not risperidone improves performance on certain cognitive-motor tasks. It is also looking to detect any negative side effects that the medicine has on children's body movements. Risperidone is often used to treat children with disruptive behaviors. This study will involve 18-20 children who are being treated by their own physicians with risperidone (for duration of 4 months or longer) for such behavior problems.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oppositional Defiant Disorder, Conduct Disorder, Attention Deficit/Hyperactivity Disorder (ADHD), Intermittent Explosive Disorder, Impulse-Control Disorders, Adjustment Disorder, Bipolar Disorder, Pervasive Developmental Disorder
Keywords
Severe conduct problems, Risperidone, Risperdal
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 3
Interventional Study Model
Crossover Assignment
Masking
Double
Allocation
Randomized
Enrollment
30 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Risperdal
Primary Outcome Measure Information:
Title
Short Term Recognition Memory task (accuracy)
Title
Titrated Delayed Matching-to-Sample task (accuracy)
Title
Continuous Performance task (omission errors)
Title
Seat Activity
Title
Graduated Holes task (errors and error times)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Aged 4 to 14 years, inclusive
Male or female gender
Reason for receiving risperidone must include severe conduct problems
Received risperidone treatment for at least 4 months
Dosage in the range of 0.01 to 0.099 mg/kg/day
Capable of discontinuing risperidone for up to 14 days in the judgement of child's physician
Taking co-therapy with psychostimulants, antihistamines, melatonin, and chloral hydrate is allowed as long as co-therapy is held constant
Taking co-therapy for sleep with guanfacine hydrochloride, clonidine hydrochloride, and trazodone hydrochloride is allowed so long as co-therapy is held constant
Must have a reliable adult carer who can report on subject's behavior and attend scheduled assessments
Parent or guardian must give informed consent, and subject must give assent if 14 years of age or older
Must be considered physically healthy on the basis of physical exam and medical history.
Exclusion Criteria:
Patients who meet DSM-IV criteria for schizophrenia, schizophreniform disorder, dissociative disorder, major depression, schizoaffective disorder, substance induced psychotic disorder
Subjects who are pregnant
Subjects with known seizure disorder
Subjects with a history of neuroleptic malignant syndrome
Subjects with a known or suspected history of severe drug allergy or hypersensitivity
Subjects must have no significant medical disease
Subjects must not be taking any other psychotropic medications.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael G Aman, Ph.D.
Organizational Affiliation
The Ohio State University Nisonger Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ohio State University Nisonger Center
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Study to Determine Whether There Are Any Cognitive or Motor Effects From Taking the Medicine Risperidone.
We'll reach out to this number within 24 hrs