NCT06851923

Brief Summary

Since the 19th century, perception has been regarded as an inferential process in which sensory input is compared with prior knowledge, namely the internalised representation of the visual environment. This notion is central to the understanding of everyday perception and cognition in general, and is attracting much attention in various areas of psychology and cognitive neuroscience. However, it is unclear whether and how the primary visual refinement that is thought to underlie the convergence of bottom-up inputs with top-down prior knowledge applies to the processing of meaningful stimuli in our everyday lives. The investigators have shown that human face processing mechanisms are shaped by prior knowledge that the horizontal range of face information conveys the richest and most reliable cues. Furthermore, investigators' previous data suggest that the primary visual cortex is recruited during the progressive refinement of face representation. Using very high field neuroimaging, the present project proposes to follow the neural mechanisms underlying the cortical refinement of horizontal information in human face processing, and to study their contribution to behaviour.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
56mo left

Started Mar 2025

Longer than P75 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress21%
Mar 2025Nov 2030

First Submitted

Initial submission to the registry

February 7, 2025

Completed
21 days until next milestone

First Posted

Study publicly available on registry

February 28, 2025

Completed
1 day until next milestone

Study Start

First participant enrolled

March 1, 2025

Completed
5.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 15, 2030

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 15, 2030

Last Updated

February 28, 2025

Status Verified

February 1, 2025

Enrollment Period

5.7 years

First QC Date

February 7, 2025

Last Update Submit

February 24, 2025

Conditions

Keywords

face perceptionMagnetic Resonance Imaging3 Teslahuman visionorientation selectivity

Outcome Measures

Primary Outcomes (4)

  • Orientation tuning in the visual system

    fMRI will be used to analyse brain responses along the ventral visual pathway to the visual presentation of orientation-filtered visual face and scene stimuli

    2 years

  • Emergence of orientation tuning over processing course in the visual system

    fMRI will be used to analyse brain responses along the ventral visual pathway to the visual presentation of temporally masked orientation-filtered visual stimuli

    2 years

  • Receptive field mapping of the visual system

    fMRI will be used to measure population receptive fields using stimuli varying in position and size randomly

    2 years

  • Behavioral task performance

    Participants will identify famous faces presented on-screen and respond via keypress.

    2 years

Study Arms (1)

Study of the visual mechanisms involved in face perception

EXPERIMENTAL
Other: 3Tesla magnetic resonance imaging of the healthy human visual system

Interventions

The present project presents a series of monocentric MRI studies carried out on healthy adult human volunteers. All neuroimaging will be performed at the Cliniques Universitaires Saint-Luc (CUSL, IRM de recherche). Participants will not directly benefit from their participation. All studies will manipulate the visual properties of the experimental stimuli in a within-subject way, and therefore do not rely on any participation group assignation/randomization method. The duration of studies will vary between 3h to 6h, i.e., from 2 to 4x1h30 3Tesla magnetic resonance imaging sessions depending on the experimental design.

Study of the visual mechanisms involved in face perception

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Be between 18 and 50 years old,
  • have normal eyesight or eyesight corrected with contact lenses,
  • Have no neurological disorder,
  • Not have had a skull fracture or head surgery,
  • Have no chronic progressive illness or mental deficiency,
  • Have no metal parts in their body (dental braces or pins, metal plates, pacemakers, implanted prostheses, etc.),
  • Have no tattoos containing metallic particles or implanted jewellery (e.g. piercings) that cannot be removed,
  • Not to have worked with metals,
  • Do not take any medicines or substances that may affect brain function (e.g. drugs, energy drinks, alcohol),
  • Not to be pregnant or breastfeeding.
  • Do not be claustrophobic.

You may not qualify if:

  • Participants presenting a counter-indication (responding yes to one of the questions of the screening questionnaire, see annex 2) to participate will be excluded from participation.
  • Participants will be screened to ascertain they do not present any of these counter-indications to the participation to the MRI measurement. We will exclude people with these characteristics:
  • Be younger than 18 or older than 50 years old,
  • have poor eyesight,
  • Have neurological disorder,
  • have had a skull fracture or head surgery,
  • Have a chronic progressive illness or mental deficiency,
  • Have metal parts in their body (dental braces or pins, metal plates, pacemakers, implanted prostheses, etc.),
  • Have tattoos containing metallic particles or implanted jewellery (e.g. piercings) that cannot be removed,
  • have worked with metals,
  • take medicines or substances that may affect brain function (e.g. drugs, energy drinks, alcohol),
  • pregnant or breastfeeding.
  • claustrophobic.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Valerie Goffaux, PhD

    Université Catholique de Louvain

    STUDY DIRECTOR
  • Mrittika Dey, Master

    Université Catholique de Louvain

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 7, 2025

First Posted

February 28, 2025

Study Start

March 1, 2025

Primary Completion (Estimated)

November 15, 2030

Study Completion (Estimated)

November 15, 2030

Last Updated

February 28, 2025

Record last verified: 2025-02

Data Sharing

IPD Sharing
Will not share