Clinical Trials in France / NCT03886584
Recruiting
Not applicable
Source Monitoring Déficit in Neuropsychiatric Population
NCT03886584 · tracked via the Priya Life Science France tracker
Condition(s) studied
Psychiatric Disorder
Investigational drug(s) / intervention(s)
Monitoring source test
Monitoring source test: Internal- and external-monitoring correct responses and inversions
Study summary
the investigators will measure source-monitoring ability in patients with several neuropsychiatric condition and in healthy controls appaired in age, sex and educational level. Source-monitoring will be measured thanks to internal- and reality-monitoring informatic tasks.The investigators hypothesized patients with fronto-temporal abnormalities would show more marked deficits than patients with only frontal abnormalities.
Eligibility
Inclusion Criteria:
* Subjects who gave their free and informed consent;
* Men and women;
* Aged 18 to 80;
* Having normal or corrected vision;
* Mastering the French language (read and spoken);
* All subjects will not have a working memory deficit preventing the test from being passed (MMSE short version):AM patients should have a score of \<MMSE \<26; Patients with pre-dementia AD will be diagnosed according to Dubois criteria (Dubois et al., 2016); patients with early FTD will be diagnosed according to Rascovsky's criteria (Rascovsky et al., 2011); Patients with DCL will be diagnosed according to McKeith's criteria (McKeith et al., 2005), TBP patients will be diagnosed using DSM 5 criteria (Arlington VA, 2013).
Exclusion Criteria:
* Inadmissibility of the consent or refusal of the subject.
* Patients under guardianship
Primary outcome measure(s)
- measure source memory performance — one year
in patients with neuropsychiatric disorders with or without temporal involvement (pre-dementia Alzheimer's disease, Alzheimer's disease - AD, fronto-temporal dementia - DFT, Lewy body dementia - DCL and bipolar disorder - TBP) and healthy volunteers matched in age, gender, and level of education.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Centre Hospitalier Le Vinatier | Bron | Auvergne-Rhône-Alpes | Recruiting |
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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 NCT03886584 on ClinicalTrials.gov ↗ ← All trials in France