Study of the Neural Basis of Analogical Reasoning

NCT02236832 — Not applicable, Completed, 130 participants, Institut National de la Santé Et de la Recherche Médicale, France

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

RegistryNCT02236832, acronym ANALOG
StatusCompleted
PhaseNot applicable
Study typeInterventional; non randomized, crossover, masking: none, basic science
Enrollment130 (Actual)
SponsorInstitut National de la Santé Et de la Recherche Médicale, France (Other gov); collaborators: Fondation pour la Recherche Médicale
ConditionsFrontotemporal Dementia, Progressive Supranuclear Palsy, Healthy Subjects
Interventionstranscranial magnetic stimulation, MRI imaging, EEG recording, Neuropsychological examination (Device, other, behavioral)
Datesstart 2015-02-01, primary completion 2021-02-01, completion 2021-02-01, first posted 2014-09-11, last updated 2025-09-04
Locations1 site in France

Related Papers Related Patents Related Grants Related Experts
All trials for Frontotemporal Dementia All trials for Progressive Supranuclear Palsy All trials of transcranial magnetic stimulation All trials of MRI imaging

-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.

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+Arms and interventions

ArmTypeInterventionsDescription
FTD (frontotemporal dementia) patientsExperimentalOther: MRI imaging; Other: EEG recording; Behavioral: Neuropsychological examinationfronto-temporal demential patients
PSP patientsExperimentalOther: MRI imaging; Other: EEG recording; Behavioral: Neuropsychological examinationprogressive supra nuclear palsy patients
healthy controlsActive comparatorOther: MRI imaging; Other: EEG recording; Behavioral: Neuropsychological examinationhealthy control education matched, age matched and sex matched with PSP and FTD patients
healthy participantsExperimentalDevice: transcranial magnetic stimulation; Other: MRI imaging; Other: EEG recording; Behavioral: Neuropsychological examinationhealthy participants that will participate to the TMS study.
healthy young participantsExperimentalOther: EEG recording; Behavioral: Neuropsychological examinationHealthy participants will be included for an EEG study
  • transcranial magnetic stimulation (Device)
  • MRI imaging (Other)
  • EEG recording (Other)
  • Neuropsychological examination (Behavioral)

+Outcome measures

Primary outcomes

  • Performance in the implicat task [day 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 task [from inclusion to 4 months after inclusion]: Reaction 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 outcomes

  • recording of EEG [day 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 MRI [day 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

+Eligibility

Sex: All, ages: 20 Years to 85 Years, accepts healthy volunteers

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.

+Locations (1)

FacilityCityCountryStatus
ICM (Institut du cerveau et de la Moelle épinière)ParisFrance

+Publications

  • Results publication: Ovando-Tellez M, Rohaut B, George N, Bieth T, Hugueville L, Ibrahim Y, Courbet O, Naccache L, Levy R, Garcin B, Volle E. Does adding <i>beer</i> to <i>coffee</i> enhance the activation of <i>drinks</i>? An ERP study of semantic category priming. Cogn Neurosci. 2022 Jan-Jun;13(2):61-76. doi: 10.1080/17588928.2021.1940117. Epub 2021 Jul 7. PMID 34232829

+Investigators