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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04562974
Other study ID # 2020-A01592-37
Secondary ID 2020-A01592-37
Status Completed
Phase N/A
First received
Last updated
Start date September 3, 2021
Est. completion date March 2, 2022

Study information

Verified date May 2022
Source University Hospital, Grenoble
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Although traditional neuropsychological models associate medial temporal lobe (MTL) regions to memory, and the hippocampus to episodic memory, there is growing evidence supporting an alternative view. The representational view of the MTL proposes that such regions depends on the representations processed rather than the cognitive processes. The aim of this project is to characterise the role played by MTL areas, and particularly the hippocampus, in mnemonic and non-mnemonic cognition. Hypotheses stemming from the representational view will thus be tested, using functional MRI among young healthy participants.


Description:

Traditional neuropsychological models associate the medial temporal lobe (MTL) with episodic memory. Further, the hippocampus would be responsible for recollection, or the rich and contextualised retrieval of a memory; whereas the perirhinal cortex (PRC) would process familiarity, or the feeling that a stimulus has been encountered before, without remembering where or when it happened. However, there is growing evidence questioning this view, and supporting an alternative proposal. The representational view of the MTL proposes that such regions would not be organised according to cognitive processes, but rather according to the representations (or the mnemonic content, represented by a pattern of neuronal spikes. A 2018-fMRI study demonstrated that the engagement of the hippocampus in recollection depends on the presence of a spatial scene in the memory that is retrieved, and not on the reconstructive nature of the retrieval. However, this demonstration is incomplete, as the only process that was investigated is recollection. The current project aims to extend such results to memory processes such as familiarity, and even to non-mnemonic processes such as visual discrimination. A fMRI study will thus be conducted, where 30 healthy participants will first perform a visual-discrimination task on scenes and objects, before taking a recognition task, in which images will either be presented in full or in the form of circular cues only. Multivariate-Pattern Analyses (MVPA) will complete traditional fMRI analyses, in order to determine whether activity in the MTL can be categorised on the basis of representations through a machine-learning classifier.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date March 2, 2022
Est. primary completion date March 2, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - Affiliation to French Healthcare system - No contraindication to MRI examination - Age between 18 and 35 years-old - Visual acuity permitting normal perception of stimuli or corrected sight Exclusion Criteria: - Existence of a pathology incompatible with the protocol : Heart, respiratory, haematological, caner, neurological disorder... - Brain-modulating medical treatment - Alcohol intake before examination - Uncorrected visual disorder - Cognitive deficit (criterion MMSE < 27) - People protected by articles L1121-5 to L1121-8 of the CSP (pregnant women, under-18 subjects, people under judiciary or administrative surveillance)

Study Design


Related Conditions & MeSH terms


Intervention

Device:
MRI-scanner
Only one group of 30 participants is constituted. All participants will perform perception and memory tasks inside a MRI-scanner. Functional activity (BOLD signal) will be registered, as well as anatomical and behavioural data.

Locations

Country Name City State
France Chu Grenoble Alpes Grenoble

Sponsors (4)

Lead Sponsor Collaborator
University Hospital, Grenoble Laboratoire de Psychologie et NeuroCognition, Université Savoie Mont Blanc, University Grenoble Alps

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hippocampal activity during behavioural tasks in the MRI scanner Activity will be recorded through the MRI whereas participants will perform the tasks. Outcome criteria consist in significant activity observed in participants hippocampus, depending on the experimental conditions. through study completion, an average of 1 year
See also
  Status Clinical Trial Phase
Recruiting NCT05847933 - Influence of Temporo-occipital Transcranial Magnetic Brain Stimulation on Aversive Episodic Memory Performance N/A