Visual Exploration and Attention: Studies in Patients With Schizophrenia and Autism Spectrum Disorders
1 other identifier
observational
140
1 country
5
Brief Summary
The aim of the protocol is to better understand the impairments in visual processing, as such impairments may induce social interaction difficulties in subjects with autism spectrum disorders (adults and children) and schizophrenia, like face exploration.The same protocol will be used for the three populations, each population being compared with matched controls. The explorations are designed to test two different hypotheses regarding the mechanisms of the visual perception difficulties of the two populations. Even though difficulties to extract the global form of objects have been described in both subjects with autism and schizophrenia, we will test two different hypotheses for the two populations. We will test the hypothesis that subjects with autism display an advantage for the processing of local information arising at an early level of processing, whereas disorders observed in patients with schizophrenia originate from attention disorders. The protocol includes three consecutive studies, each one being applied in each of the three populations.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jun 2009
Longer than P75 for all trials
5 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2009
CompletedFirst Submitted
Initial submission to the registry
June 2, 2009
CompletedFirst Posted
Study publicly available on registry
June 4, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2016
CompletedAugust 26, 2016
August 1, 2016
7.5 years
June 2, 2009
August 25, 2016
Conditions
Keywords
Study Arms (6)
A1
Patients with schizophrenia
A2
Control subjects matched individually with patients with schizophrenia
B1
Adult subjects with autism
B2
Control subjects matched individually with adult subjects with autism
C1
Children with autism
C2
Control subjects matched individually with children with autism
Interventions
Study one: global/local processing, with a neutral prime (stimulus influencing the processing of the subsequent stimulus)Study two: global/ local processing with a prime whose elements are collinear.Study three: global/local processing with a prime whose elements are not collinear
Eligibility Criteria
Psychiatry clinic in Strasbourg and Brumath. Pedopsychiatry Clinic in Strasbourg. Residents of Strasbourg and Brumath
You may qualify if:
- IQ above 70, as evaluated with the WAIS III in adults and with the WISC in children
- signed consent
- DSM IV criteria in case of autism spectrum disorders or schizophrenia
You may not qualify if:
- grave or non stabilized somatic pathology
- pathology affecting the central nervous system; other than the studied pathologies
- intake of psychotropic drug, except for patients
- invalidating sensory processes
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (5)
Pôle départemental du Centre de Ressources Autisme pour adultes (67) - Etablissement public de santé Alsace-Nord (site de Brumath)
Brumath, 67170, France
Centre de Ressources Autisme Pôle adultes (68) - Espace Autisme 68
Colmar, 68000, France
Clinique Lautréamont
Loos, 59120, France
Pôle régional du Centre de Ressources Autisme pour enfants et adolescents - Unité d'évaluation des troubles du développement Hôpital de l'Elsau - Pôle de Psychiatrie - Unité d'évaluation des troubles du développement Hôpital de l'Elsau - HUS
Strasbourg, 67000, France
INSERM U666 ; Pôle de Psychiatrie - Service de Psychiatrie Adulte- HUS
Strasbourg, 67091, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Anne GIERSCH
Institut National de la Santé Et de la Recherche Médicale, France
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 2, 2009
First Posted
June 4, 2009
Study Start
June 1, 2009
Primary Completion
December 1, 2016
Study Completion
December 1, 2016
Last Updated
August 26, 2016
Record last verified: 2016-08