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Functional MRI of Cognitive Control in Autism

This study is not yet open for participant recruitment.
Verified by UMC Utrecht, April 2007

Sponsored by: UMC Utrecht
Information provided by: UMC Utrecht
ClinicalTrials.gov Identifier: NCT00463164
  Purpose

This study aims to investigate the role of fronto-striatal circuits and cognitive control in the perseverative and inflexible behavior that is a defining feature of autism. We hypothesize that deficits in the development of fronto-striatal circuitry may underlie cognitive inflexibility in autism. Specifically, we hypothesize that repetitive, inflexible behavior arises as (1) fronto-striatal systems are capable of learning patterns present in the environment (as in implicit learning paradigms), but are unable to adapt behavior to changing circumstances, related to either (2) decreased ability of basal ganglia to detect violations of expectancy, (3) decreased ability of prefrontal cortex to respond to detected violations, or (4) decreased connectivity of the circuits. We are conducting three functional Magnetic Resonance Imaging (fMRI) studies to address these hypotheses.


Condition
Autism

MedlinePlus related topics:   Autism   

U.S. FDA Resources

Study Type:   Observational
Study Design:   Natural History, Cross-Sectional, Case Control, Prospective Study
Official Title:   Functional MRI of Cognitive Control in Autism

Further study details as provided by UMC Utrecht:

Estimated Enrollment:   90
Study Start Date:   December 2007

  Eligibility
Ages Eligible for Study:   6 Years to 12 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria:

  • Aged 6 - 12 years at inclusion

Inclusion criteria for subjects with autism

  • DSM-IV (APA, 1994) diagnosis of autism, according to ADI-R interview

Inclusion criteria for controls

  • No DSM-IV (APA, 1994) diagnosis, according to DISC interview
  • No scores in the clinical range on the Child Behavior Checklist (CBCL) and Teacher Rating Form (TRF)
  • IQ > 70

Exclusion Criteria:

  • Major illness of the cardiovascular, the endocrine, the pulmonal or the gastrointestinal system
  • Presence of metal objects in or around the body (pacemaker, dental braces)
  • History of or present neurological disorder
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00463164

Contacts
Contact: Sarah Durston, Ph.D.     +31 30 250 8161     S.Durston@umcutrecht.nl    

Locations
Netherlands
Dept. of Child and Adolescent Psychiatry, UMC Utrecht     Not yet recruiting
      Utrecht, Netherlands, 3584CX
      Principal Investigator: Tamar van Raalten, M.Sc.            

Sponsors and Collaborators
UMC Utrecht

Investigators
Principal Investigator:     Sarah Durston, Ph.D.     Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht    
Study Chair:     Herman van Engeland, M.D. Ph.D.     Rudolf Magnust Institute of Neuroscience, UMC Utrecht    
  More Information


Lab homepage with info for subjects (in Dutch)  This link exits the ClinicalTrials.gov site
 
Lab homepage with info in English  This link exits the ClinicalTrials.gov site
 

Study ID Numbers:   06-179
First Received:   April 19, 2007
Last Updated:   April 19, 2007
ClinicalTrials.gov Identifier:   NCT00463164
Health Authority:   Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)

Keywords provided by UMC Utrecht:
functional MRI  

Study placed in the following topic categories:
Child Development Disorders, Pervasive
Developmental Disabilities
Mental Disorders
Autistic Disorder
Mental Disorders Diagnosed in Childhood

ClinicalTrials.gov processed this record on October 10, 2008




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