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Starting soon Not applicable

Neural Mechanisms of Emotion-behaviour Interactions

NCT07623746 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-12-01
Last updated
2026-10-07

Condition(s) studied

Healthy Volunteer

Investigational drug(s) / intervention(s)

Functional Magnetic Resonance Imaging (fMRI)

Functional Magnetic Resonance Imaging (fMRI): Participants will perform a cognitive task (responses through button presses) while we measure brain activity with functional magnetic resonance imaging (fMRI) and record their facial expressions.

Study summary

Deciding what to do when for how long - self-organizing one's behaviour - is an important feature of daily life. Emotions arise providing short-cuts for the computational complexities. Yet, one still knows relatively little about the underlying cognitive and neural mechanisms. EMOBB will establish the computational, cognitive and neural underpinnings of the rich interplay between emotions and self-organized behaviour in naturalistic environments. Previous work has almost exclusively relied on tasks structured into experimenter determined trials - thus how people self-organized behaviour could not be measured. To overcome this, EMOBB will combine novel naturalistic tasks in which people have freedom what to do when for how long with subjective and objective measurements of emotions. This will be made possible through a computational modelling approach that allows dissecting and quantifying even complex behaviour-emotion interactions.

Specifically, EMOBB will use three cognitive tasks of emotion-behaviour interplay that participants will do while undergoing functional magnetic resonance brain imaging and monitoring of their facial expressions with an MRI-compatible camera.

The primary hypothesis of EMOBB is that both unique and shared neural networks will underpin the interplay between emotions and behaviour across our cognitive tasks.

Eligibility

Sex
ALL
Min age
18 Years
Max age
45 Years
Healthy volunteers
Accepted
Inclusion Criteria: * 18-45 years old, * fluent French speakers, * healthy, * without a beard at the time of testing, * right-handed, * being able to use both hands * BMI between 18.5 and 30 * give written informed consen * for women: contraception; Exclusion Criteria: * neurological, psychiatric disorders, or severe chronic disorders (diabetes, cardiac, kidney, lung, liver disorders, inflammatory disorders) * pregnancy or breast-feeding * under guardianship, currently admitted to a psychiatric hospital other than for research purposes) * not wanting to be informed of abnormalities detected during MRI scan, * taking part in other studies with exclusion periods, * MRI exclusion criteria (cardiac pace maker etc, vascular or intracranial clamps or stents, neurological stimulator, any other metal in the body, past accidents with metal to the eyes, metallic prostheses, metal in the mouth (braces, retainers), medication pumps, any implants (e.g. hearing implants), piercings that cannot be removed, having worked with metal (other than radiography related to MRI) being claustrophobic, tatoos above the shoulders.

Primary outcome measure(s)

  • Brain activity in regions of interest — Day 0
    Brain activity is captured as percentage change in blood-oxygen-level-dependent (BOLD) signal with FMRI compared to baseline across tasks across brain regions (ventromedial prefrontal cortex, vmPFC; dorsal anterior cingulate cortex, dACC).

Trial sites (1)

FacilityCityRegionStatus
CERMEP (Centre d'Etude de Recherche Multimodal et pluridisciplinaire en imagerie du vivant) Bron France
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 NCT07623746 on ClinicalTrials.gov ↗ ← All trials in France