Source Monitoring Déficit in Neuropsychiatric Population
Recruiting · NCT03886584 · Interventional (participants receive a specific treatment) · Lead sponsor: Hôpital le Vinatier
View the official record on ClinicalTrials.gov →Interventions studied
Monitoring source test
What this trial is about
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.
Who can take part
Age range
18 Years to 80 Years
Sex
All (male and female)
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
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
Where it is running
1 location listed.
- Centre Hospitalier Le Vinatier - Bron, Auvergne-Rhône-Alpes, France