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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04278339
Other study ID # 19-PP-14
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 10, 2020
Est. completion date October 2025

Study information

Verified date June 2023
Source Centre Hospitalier Universitaire de Nice
Contact Bruno GIORDANA, PH
Phone 4.92.03.87.75
Email giordana.b@chu-nice.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Disorders of social cognition, and empathy more specifically, are at the heart of schizophrenic pathology in that they are strongly linked to the social handicap of patients. It is therefore necessary to refine our knowledge of the cognitive and affective processes behind this empathic disorder and to identify objective and easily measurable markers (related to brain functioning collected by electroencephalography) of these processes with the subsequent aim of improving their management. It is also relevant to question the trait/status nature of these empathic disorders by studying these markers in individuals presenting more or less marked schizotypic traits and therefore more or less at risk of developing schizophrenia. Studying the possibility that empathy disorders may be part of the factors of developmental vulnerability for schizophrenia and identifying objective markers of this vulnerability could allow, in case of development of the pathology, a more rapid diagnosis and a more effective management.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date October 2025
Est. primary completion date October 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Common to all: good command of the French language, right-handed. - Specific to patients: diagnosis of schizophrenia or schizoaffective disorder, clinical state stabilized according to the treating psychiatrist. Exclusion Criteria: - Common to all: having suffered a head injury with loss of consciousness lasting more than 5 minutes, participating in another project at the time of the present study, presenting an addiction to a toxic substance (excluding tobacco), presenting a mental retardation or neurological disorder (verified by a pre-recruitment interview and the administration of the Mini International Neuropsychiatric Interview for control subjects and on the basis of the information in the medical file for patients). - Patient-specific: significant change (according to the doctor) in treatment in the previous month, currently hospitalized. - Specific to controls: taking a psychoactive drug, having a mental disorder, being first-degree related to a patient with a disorder other than schizophrenia or schizoaffective disorder.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Evoked Related Potentials
Evoked Related Potentials are measured by means of electroencephalography. During this measure, 2 informatic task will be performed to evaluated evoked related potentials.

Locations

Country Name City State
France Hôpital Pasteur - Service de Psychiatrie Nice

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nice

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evoked Related Potentials Amplitude of modulations of the electrophysiological signal On the first day
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