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Study of the Neural Basis of Analogical Reasoning

Organisation du Cortex préfrontal ventrolatéral Pour l'Analogie: Approche Bimodale Chez le Sujet Sain et Chez le Patient Ayant un Syndrome Frontal.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02236832
Acronym
ANALOG
Enrollment
130
Registered
2014-09-11
Start date
2015-02-28
Completion date
2021-02-28
Last updated
2025-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frontotemporal Dementia, Progressive Supranuclear Palsy, Healthy Subjects

Brief summary

Frontal patients are impaired in categorisation and analogical reasoning tasks, and different functional imaging studies from our group have shown the involvement of the prefrontal cortex in categorisation and analogy tasks. The aim of this project is to test our hypotheses about the role of the prefrontal cortex in explicit and implicit categorisation and analogy tasks.

Interventions

DEVICEtranscranial magnetic stimulation

Sponsors

Fondation pour la Recherche Médicale
CollaboratorOTHER
Institut National de la Santé Et de la Recherche Médicale, France
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

Healthy subjects: * subject affiliated to national health insurance * informed consent signed * normal neurological examination * subject aged at least 20 Patients: * FTD or PSP diagnostic criteria filled * patient affiliated to national health insurance * informed consent signed

Exclusion criteria

* Severe psychiatric symptomatology and psychotropic drug use * unability to understand or perform the cognitive tasks.

Design outcomes

Primary

MeasureTime frameDescription
Performance in the implicat taskday of inclusion (one day)Reaction time and accuracy will be registered for this categorization task. This task will be used in patients with FTD and in healthy controls (n=60). Participants will come only once during one day ot the research centre.
Performance in the Similitude taskfrom inclusion to 4 months after inclusionReaction time and accuracy will be recorded while healthy subjects perform this categorization task, after a session of rTMS or during on line TMS (n=40). Participants will come 3 to 5 times at the research centre in a maximum period of 4 months.

Secondary

MeasureTime frameDescription
recording of EEGday of inclusion (one day)EEG will be recorded in patients with FTD and in healthy controls for an analysis of event related potentials. Participants will come only once during one day a the research centre.
Analysis of MRIday of inclusion (one day)T1 MRI will be recorded for VBM analysis in patients with FTD and healthy controls. Participants will come only once during one day at the research centre

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026