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Recruiting Not applicable

NeuroCognitive Bases of Tool Use

NCT04566744 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2021-11-08
Last updated
2024-06-25

Condition(s) studied

Healthy

Investigational drug(s) / intervention(s)

fRMI

fRMI: The measurements performed will be the participant's brain activity, as well as behavioral measurements associated with the tasks performed (response time, correctness of the response). Brain activity measurements will be performed on the Siemens 3T system of the MRI department of CERMEP. The subject will perform the task under study while the level of brain activity is recorded. The functional examination will be subdivided into several parts according to its total length in order to spare the subject. The total duration of MRI acquisitions will be approximately 1 hour regardless of the axis.

Study summary

Tool use is considered to be the hallmark of complex cognitive adaptations that humans have achieved trough evolution, that provides an adaptive advantage to the human species. Even if nonhuman species do use tools too, human tool use is much more complex and sophisticated. If humans have special abilities for tool use, it has to be grounded in a specific neuroanatomical substrate. Humans and nonhumans share a similar prehension system located within the superior parietal lobe and the intraparietal sulcus. However, there is a human specificity: the supramarginal gyrus within the left inferior parietal lobe is unique to humans, and could play a central role in tool use. This project aims to study the neurocognitive bases of human tool use with functional Magnetic Resonance Imaging (fMRI), to precise the cognitive mechanisms through which humans are able to use tools.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * To be between the ages of 18 and 65 years old * Having given an informed consent for the study Exclusion Criteria: * Pregnant or breastfeeding woman * Persons under curators or deprived of civil rights or deprived of their freedom * Not being registered with the French Social Security System * Not able to read/write the French * Neurologic or psychiatric illness, known or revealed during the inclusion visit * Substance intake ( taking psychoactive medications or recreational drugs) on the day of the experiment * Noise intolerance * Unable to fill a questionnaire (severe cognitive troubles) * Not willing that their personal doctor to be informed in case of a MRI anomaly. * Not willing to be informed in case of MRI anomaly * Subjects must not have metallic or electronic implants in the body : pacemakers or pacemaker wires, open heart surgery, artificial heart valve, brain aneurysm surgery, middle ear implant, hearing aid, braces or extensive dental work, cataract surgery or lens implant, implanted mechanical or electrical device, or artificial limb or joint o foreign metallic objects in the body (bullets, pellets, shrapnel, or metalwork fragments) or current or past employment as machinists, welders or metal workers, tattoos near the head or neck regions, permanent makeup * Not willing to complete the study * Appearance of a exclusion criterion during the protocol * Appearance of an undesirable event preventing the completion of the protocol * Too great head movements (\>4mm for the session) * Detection of artifacts in the brain images collected

Primary outcome measure(s)

  • Blood Oxygenation Level Dependent measure — 1 hour
    The primary outcome measure will be the Blood Oxygenation Level Dependent measure (BOLD) as permitted with functional Magnetic Resonance Imaging.This BOLD level will be collected for every voxel in the imaged brain, and at regular time intervals (TR = 3s) during the experimental session (about one hour). This is standard procedure for fMRI experiments. FMRI measures brain activity by detecting changes associated with blood flow. This technique relies on the fact that cerebral blood flow and neuronal activation are coupled. When an area of the brain is in use, blood flow to that region also increases. The primary form of fMRI uses the BOLD contrast in response to an experimental condition (Ogawa, Lee, Kay, \& Tank, 1990), allowing researchers to track changes in oxygen consumption on the brain and therefore brain activity. BOLD effefct is computed by assessing the different relaxation times (T1 and T2) in the brain, as T1 and T2 are different in function of regional cerebral blood flows

Trial sites (1)

FacilityCityRegionStatus
CERMEP Bron France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04566744 on ClinicalTrials.gov ↗ ← All trials in France