An interventional study of Questionnaire and Cognitive tests in Schizophrenia, sponsored by Hôpital le Vinatier. Recruiting at 1 site in France. Open to participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-11.
Sponsored by Hôpital le Vinatier · Not applicable, Interventional, and Other
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Among 32 studies in Schizophrenia by Hôpital le Vinatier — 6 open to participants now, 6 under way, none of them phase 3. Schizophrenia · Hôpital le Vinatier.
Among the 32 studies in Schizophrenia by Hôpital le Vinatier, this one is the 7th largest by planned enrollment of the 31 interventional ones that give a count, is one of 3 that started in 2020, is one of 31 with no phase, and was the 25th registered.
3,567 studies on the registry are indexed under Schizophrenia; 493 are open to participants now.
Browse Schizophrenia studies →6 of the 32 studies in Schizophrenia by Hôpital le Vinatier are open now, in 1 country. Recruiting first, the newest first:
Hôpital le Vinatier · Sites in France
Ages 18+
Hôpital le Vinatier · Sites in France
Ages 45–80
Hôpital le Vinatier · Sites in France
Ages 18–40
Hôpital le Vinatier
Ages 18–65 · Healthy volunteers
Hôpital le Vinatier · Sites in France
Ages 18–50
By country, each count listing its studies:
Of the 332 Schizophrenia studies recruiting now, 63 (19%) set no upper age limit and 258 (78%) stop at 75 or younger; 42 take children under 18; 83 take healthy volunteers.
This study: 18 Years to 45 Years · all sexes · healthy volunteers too.
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32 studies; the count open now beside each. This study's row is marked.
First in 2006; this study’s year is marked. 3 started in 2020.
This study's planned enrollment of 120 is above the median of 71 across 2,947 interventional studies indexed under Schizophrenia.
Median enrollment 60 across the 31 interventional studies, 515 across the 1 observational. Of the 24 that completed or were terminated, 0 (0%) have results posted.
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Hôpital le Vinatier is the lead sponsor of 106 studies on the registry; 41 are open to participants now.
2 of the studies in Schizophrenia by Hôpital le Vinatier that are under way reach primary completion within a year, 0 of them phase 3. Phase 3 first, then by date:
| Study | Primary completion |
|---|---|
| NCT04237155Hôpital le VinatierFrench Source-monitoring Task | 2027-02-01 |
| NCT04946916Hôpital le VinatierNeurofilament Light Chains and Cognitive Impairment in Chronic Psychiatric Disease | 2027-03-22 |
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Among the 32 studies in Schizophrenia by Hôpital le Vinatier, from their registry updates:
Nothing recorded among them since 2026-09-25.
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Source-monitoring is a cognitive process that refers to the ability to remember the source of an information. Source-monitoring processes are usually studied using experimental behavioral tasks. These tasks, which are very heterogeneous, are not all available in French and, for the most part, cannot be used in neuroimaging protocols.
The aim of this project is to develop an experimental task which allows the measurement of source-monitoring performances, and which is adapted to neuroimaging protocols in a French-speaking population.
The study will include 2 steps: 1) validation of the verbal material necessary for the creation of the source-monitoring task and 2) testing the task.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
The American Psychiatric Association’s manual of mental health diagnoses. DSM-5 (2013, revised as DSM-5-TR in 2022) replaced DSM-IV, and some studies still name the older edition. “Meets DSM criteria for …” means diagnosed by that edition’s diagnostic criteria, usually by a clinician in an interview.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
DSM diagnostic criteria
The American Psychiatric Association’s manual of mental health diagnoses. DSM-5 (2013, revised as DSM-5-TR in 2022) replaced DSM-IV, and some studies still name the older edition. “Meets DSM criteria for …” means diagnosed by that edition’s diagnostic criteria, usually by a clinician in an interview.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
30 healthy individuals will complete a verbal material scoring questionnaire
Other: Questionnaire
30 patients with schizophrenia will complete a verbal material scoring questionnaire
Other: Questionnaire
30 healthy individuals will complete the source-monitoring task which will be created from step 1 as well as the task of reference
Other: Cognitive tests
30 patients with schizophrenia will complete the source-monitoring task which will be created from step 1 as well as the task of reference
Other: Cognitive tests
Subjects will complete a verbal material scoring questionnaire
Subjects will complete two source-monitoring tasks: the source-monitoring task which will be created from step 1 as well as the task of reference
Source-monitoring performances
Performances (calculated as the number of accurate source responses and the number of errors) obtained at the new source-monitoring task and at the source-monitoring task of reference (Brunelin et al., 2006).
Time frame: one day
Plan to share: Undecided
No publications or documents are linked to this record.
Started Feb 2020 (actual). Primary completion is estimated for Feb 2027, 83 months after the start.
Of 756 non-industry interventional studies with no phase under Schizophrenia, half reached primary completion within 33 months of starting (the median), counting those still running; a quarter within 17 and three quarters within 56. This study's planned 83 months is above that.
Counting every sponsor, half of 769 studies reached it within 32 months; a quarter within 16 and three quarters within 56.
How these figures are worked out, and which studies are left out of them.
Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.
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