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Clinical Trials in France / NCT03649581
Recruiting Not applicable

Investigation of Neurophysiological Markers, Possibly Specific of Two Subforms of Psychotic Disorders

NCT03649581 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2019-02-28
Last updated
2025-08-03

Condition(s) studied

Schizophrenia

Investigational drug(s) / intervention(s)

compare the two groups of schizophrenic patientscompare the two groups of schizophrenic patients versus volunteers

compare the two groups of schizophrenic patients: Compare two groups of markers relating respectively to psychomotricity and affectivity in two subforms of schizophrenia: periodic catatonia and hebephrenia in order to highlight a possible double dissociation: 1. abnormalities of markers related to affectivity in Hebephrenia (with preservation of these markers in periodic catatonia), 2. abnormalities of markers related to psychomotricity in periodic catatonia (with markers of these tests in Hebephrenia).

compare the two groups of schizophrenic patients versus volunteers: compare the results of the schizophrenic patient group with healthy volunteers

Study summary

The current diagnostic criteria for schizophrenia and other psychotic disorders are relatively broad and lack precision. Therefore, distinct diseases may be grouped together under the same diagnostic category, although these diseases may differ according to their clinical expression, prognosis and perhaps their physiopathological causes.

We think that identifying subforms of psychotic disorders that are more homogeneous will better enable to understand their respective physiopathological causes and find personalized treatments.

This study will compare two subforms of psychotic disorders that have been clinically distinguished in the 1970s. These phenotypes have however not been validated yet using scientific investigations.

Using clinical assessments, cognitive evaluations and neurophysiological measures (fMRI) investigating the domains of affect and psychomotoricity , we expect that these two subforms will differ on their clinical, cognitive and neurophysiological characteristics, namely: hebephrenia will be associated with deficits on the affect markers , and respect psychomotoricity (catatonia scales, tests assessing movement planification) whereas the opposite pattern will be observed for periodic catatonia.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * for both patients and controls * male or female willing to participate and who have signed up the legal document * under the protection of health insurance for patients only * schizophrenia or schizo-affective disorder according to the DSM-5 criteria * periodic catatonia or hebephrenia accordin to WKL classification * clinically stable for at least 2 months * in or out patients for controls only * no psychiatric history Exclusion Criteria: * for both patients and controls * current severe or unstable somatic illness * neurological history (epilepsia, brain injury, brain surgery…) * current substance use disorder (DSM-5) * current major depressive disorder (DSM-5) * mental retardation (IQ \< 70) * pregnancy, breast feeding * current legal control * contra-indication for fMRI for controls only psychotropic intake during the last 3 weeks

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Service de Psychiatrie I, Hôpital Civil, Hôpitaux Universitaires de Strasbourg Strasbourg France Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03649581 on ClinicalTrials.gov ↗ ← All trials in France