Attention and Visual Perception in Schizophrenia: A Functional Magnetic Resonance Imaging (fMRI) Study
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Purpose
The main objective of the study is to contribute to a better understanding of the physiopathology of schizophrenia, by studying causal relationships between cognitive deficits and the neurobiological basis for these deficits. Processing visual information involves both automatic grouping processes and control processes. Automatic grouping processes allow the building of a global configuration from local contour information. It is necessary in order to recognize objects. Control processes allow tending to and prioritizing information parts. The paradigm the investigators use allows to dissociate these processes, and is used in order to characterize the impairments observed in patients with schizophrenia. It is adapted to fMRI in order to explore the neurobiological basis of the deficits. The investigators will examine whether functional disconnectivity between activated areas subtend the impairments observed in patients.
| Condition | Intervention |
|---|---|
|
Schizophrenia |
Procedure: fMRI |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Prospective |
| Official Title: | Attention and Grouping of Visual Information: What is Disturbed in Patients With Schizophrenia? |
| Estimated Enrollment: | 52 |
| Study Start Date: | September 2006 |
| Study Completion Date: | April 2009 |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
Healthy volunteers
Healthy controls
|
Procedure: fMRI
One 30 minute session
|
|
Patients
Patients with schizophrenia
|
Procedure: fMRI
One 30 minute session
|
Eligibility| Ages Eligible for Study: | 18 Years to 50 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Primary care clinic, residents of Strasbourg
Inclusion Criteria:
- Patients with schizophrenia (DSM-IV criteria)
- Healthy controls matched with patients on age, sex and education level
- Ages 18 to 50
- Signed informed consent
- Right-handed
Exclusion Criteria:
- No severe somatic illness
- No invalidating sensory disease
- No drug abuse, as defined by DSM-IV criteria
- No general anaesthesia in the past 3 months
- No intake of drugs affecting the CNS, except for patients
Contacts and Locations| France | |
| Inserm U666 - Département de Psychiatrie, Hôpitaux Universitaires de Strasbourg | |
| Strasbourg, France, 67091 | |
| Principal Investigator: | Anne Giersch, MD | Institut National de la Santé Et de la Recherche Médicale, France |
More Information
No publications provided
| Responsible Party: | Emmanuel LAVOUE, Directeur Adjoint de la DRCI, University Hospital, Strasbourg, France |
| ClinicalTrials.gov Identifier: | NCT00350935 History of Changes |
| Other Study ID Numbers: | 3456 |
| Study First Received: | July 10, 2006 |
| Last Updated: | June 25, 2010 |
| Health Authority: | France: Ministry of Health |
Keywords provided by University Hospital, Strasbourg, France:
|
fMRI Visual perception Attention |
Additional relevant MeSH terms:
|
Schizophrenia Schizophrenia and Disorders with Psychotic Features Mental Disorders |
ClinicalTrials.gov processed this record on June 17, 2013