The Influence of Collective Schemas on Individual Memory
Overview
Schemas describe mental structures storing recurrent and organized pattern of information. Schemas may have a strong influence on the process of storing and retrieving new information into memory. Previous approaches in the cognitive neuroscience of memory have entirely focused on the individual dimension of preexisting schemas. In the real world though, much of the researchers' experiences and knowledge are collective or shared. Such social-cultural frameworks stored in collective memory may also reshape and reconfigure the construction of individual memories. Attempting to ascertain the influence of collective schema on the neural substrates of individual memories using cutting-edge brain imaging methods represents the challenge that MULTIBRAIN2 seeks to tackle. To achieve this goal, the researchers will record brain activity during MRI scanning sessions in a group of 24 participants while they are performing an encoding followed by episodic memory retrieval tasks on pictures of the World War II Memorial of Caen. This study will seek to identify brain areas of the prefrontal cortex encoding the organization of knowledge in collective memory using multivariate analyses of brain activity patterns, and then to understand how such regions might modulate the recruitment of the hippocampus during episodic memory retrieval using analyses of effective connectivity. The organization of knowledge in collective memory is measured in parallel through 1) the analysis of French social memory of World War II using a corpus of thousand of television and radio shows from the National Institute of Audiovisual, and 2) an internet task measuring the organization of shared individual knowledge about World War II. Once collected, these data will help us to understand how collective schemas may shape the organization of individual memories.
Full Title of Study: “ETUDE D’IMAGERIE PAR RESONANCE MAGNETIQUE FONCTIONNELLE CHEZ LE SUJET SAIN DES RELATIONS ENTRE MEMOIRE COLLECTIVE ET INDIVIDUELLE”
Study Type
- Study Type: Interventional
- Study Design
- Allocation: N/A
- Intervention Model: Single Group Assignment
- Primary Purpose: Basic Science
- Masking: None (Open Label)
- Study Primary Completion Date: June 1, 2017
Interventions
- Behavioral: Episodic memory task
- Device: fMRI
Arms, Groups and Cohorts
- Experimental: Healthy participants
Clinical Trial Outcome Measures
Primary Measures
- Blood Oxygen Level Dependent (BOLD) response as measured with fMRI
- Time Frame: 1 hour
Participating in This Clinical Trial
Inclusion Criteria
- Healthy participants between 20 and 38 years old – Affiliated to the French national health care system – French native speaker – Having not visited the Memorial of Caen for the past four years – Right-handed – At least 2 years of education after graduating from high school – Body mass < 30kg/m2 – Signed written consent form Exclusion Criteria:
- Pregnancy or intent to get pregnant – Person deprived of their liberty – Person hospitalized without consent – Minor – Protected adults or people unable to give informed consent – Person subjected to an exclusion period related to another protocol – History of neurological or psychiatric disorders or existence of traumatic brain injury with loss of consciousness for more than one hour – History of cancer with the last 5 years, excluding squamous cell carcinomas – Alcoholism, antecedents of chronic alcoholism or drugs abuse – Severe psychiatric disorders (according to DSM V diagnostic criteria) or psychological troubles which could affect participant's judgment – Use of medication that may interfere with cognitive or cerebral functioning – Presence of visual or hearing troubles that may compromise participant's ability to participate in the study – MRI Contraindications
Gender Eligibility: All
Minimum Age: 20 Years
Maximum Age: 38 Years
Are Healthy Volunteers Accepted: Accepts Healthy Volunteers
Investigator Details
- Lead Sponsor
- Institut National de la Santé Et de la Recherche Médicale, France
- Collaborator
- La Région Basse-Normandie
- Provider of Information About this Clinical Study
- Sponsor
- Overall Official(s)
- Fausto Viader, PUPH, Principal Investigator, University Hospital, Caen
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