Source Monitoring Déficit in Neuropsychiatric Population
Recruiting now · Not applicable
Conditions studied: Psychiatric Disorder
In brief
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.
Key facts
- Study ID
- NCT03886584
- Run by
- Hôpital le Vinatier
- People needed
- 300
- Starts
- 2019-03-08
- Expected to finish
- 2026-07-31
- Last updated by the study team
- 2025-07-31
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- 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).
You may not qualify if…
- Inadmissibility of the consent or refusal of the subject.
- Patients under guardianship
Where it is running
- Centre Hospitalier Le Vinatier — Bron, Auvergne-Rhône-Alpes, France (enrolling)
Full record on ClinicalTrials.gov
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