Bipolar Disorder Clinical Trial
Official title:
Effects of Risperidone on Cognitive-Motor Performance and Motor Movements in Chronically Medicated Children
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:
1. Risperidone will have no adverse effects on cognitive-motor performance in children who
have received maintenance therapy for 4 to 20 months.
2. Children tested during placebo will show no more dyskinetic movements than during
risperidone treatment (i.e., there will be no unmasking of tardive dyskinesia).
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medicines is largely negative (although limited in amount) and frequently badly out of date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.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Diagnostic
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05111548 -
Brain Stimulation and Cognitive Training - Efficacy
|
N/A | |
Completed |
NCT02855762 -
Targeting the Microbiome to Improve Clinical Outcomes in Bipolar Disorder
|
N/A | |
Recruiting |
NCT05915013 -
Alpha-Amino-3-Hydroxy-5-Methyl-4- Isoxazole Propionic Acid Receptor Components of the Anti-Depressant Ketamine Response
|
Phase 1 | |
Recruiting |
NCT05206747 -
Ottawa Sunglasses at Night for Mania Study
|
N/A | |
Completed |
NCT02513654 -
Pharmacokinetics, Safety and Tolerability of Repeat Dosing Lamotrigine in Healthy Chinese Subjects
|
Phase 1 | |
Recruiting |
NCT06313918 -
Exercise Therapy in Mental Disorders-study
|
N/A | |
Completed |
NCT02304432 -
Targeting a Genetic Mutation in Glycine Metabolism With D-cycloserine
|
Early Phase 1 | |
Recruiting |
NCT06197048 -
Effect of Nutritional Counseling on Anthropometry and Biomarkers in Patients Diagnosed With Schizophrenia/Psychosis or Bipolar Affective Disorder
|
N/A | |
Completed |
NCT03497663 -
VIA Family - Family Based Early Intervention Versus Treatment as Usual
|
N/A | |
Completed |
NCT04284813 -
Families With Substance Use and Psychosis: A Pilot Study
|
N/A | |
Completed |
NCT02212041 -
Electronic Cigarettes in Smokers With Mental Illness
|
N/A | |
Recruiting |
NCT05030272 -
Comparing Two Behavioral Approaches to Quitting Smoking in Mental Health Settings
|
N/A | |
Recruiting |
NCT04298450 -
ED to EPI: Using SMS to Improve the Transition From the Emergency Department to Early Psychosis Intervention
|
N/A | |
Active, not recruiting |
NCT03641300 -
Efficacy of Convulsive Therapies for Bipolar Depression
|
N/A | |
Not yet recruiting |
NCT04432116 -
Time and Virtual Reality in Schizophrenia and Bipolar Disorder
|
N/A | |
Terminated |
NCT02909504 -
Gao NARASD Lithium Study
|
Phase 4 | |
Completed |
NCT02970721 -
Use of Psychotropic Medications Among Pregnant Women With Bipolar Disorder
|
||
Terminated |
NCT02893371 -
Longitudinal Comparative Effectiveness of Bipolar Disorder Therapies
|
||
Recruiting |
NCT03088657 -
Design and Methods of the Mood Disorder Cohort Research Consortium (MDCRC) Study
|
||
Recruiting |
NCT02481245 -
BezafibrateTreatment for Bipolar Depression: A Proof of Concept Study
|
Phase 2 |