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Imaging During Subliminal Perception

Functional Imaging During Subliminal Perception

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04643340
Enrollment
70
Registered
2020-11-25
Start date
2020-03-15
Completion date
2022-12-01
Last updated
2023-06-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

functional MRI, subliminal perception, EEG, neurofeedback, attention

Brief summary

Subliminal perception of visual stimuli can be studied with functional brain imaging, e.g. with functional magnetic resonance imaging (fMRI). However, it is unclear how subliminal perception affects connectivity in the brain. Further, it is not known if real-time (rt) fMRI neurofeedback of brain areas involved in subliminal perception can lead to supra-threshold perception. For attention tasks, the investigators hypothesize that functional connectivity strength is mediated by the insular cortex during both supra-threshold and subliminal perception. Additionally, the investigators hypothesize that rt-fMRI neurofeedback training should alter neuronal and behavioral responses.

Detailed description

In this project, using healthy adults, the investigators have 2 aims: 1. Apply electroencephalography (EEG) and fMRI before and after rt-fMRI neurofeedback during attention tasks to identify brain regions involved in subliminal and supraliminal perception. 2. Apply functional connectivity analyses during these tasks.

Interventions

Brain regions can be trained, i.e. fMRI activity can be actively modulated online by humans, using rt-fMRI (Bruhl, Scherpiet et al. 2014, Bruhl 2015, Emmert, Kopel et al. 2016).

Sponsors

Swiss National Science Foundation
CollaboratorOTHER
University of Zurich
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy adults (\> 18 \< 80 years), which can read and sign the informed consent form * Male and female * Right-handed

Exclusion criteria

* metallic items in the body (i.e. eye splinter, MR incompatible implants) * pacemaker * claustrophobia * pregnant participants * participants suffering from a degenerative disorder of the Central Nervous System, such as Stroke, Multiple Sclerosis, Parkinson's Disease, Alzheimer's Disease and Huntington's Disease and with major psychiatric disorders such as schizophrenia, depression, or anxiety disorder * Drug intake (psychopharmaca)

Design outcomes

Primary

MeasureTime frameDescription
fMRI during supra-threshold and subliminal perception2020 - 2022
rt-fMRI activity2020 - 2022rt-fMRI activity: fMRI signal changes during repetitive real time fMRI based training

Secondary

MeasureTime frameDescription
Functional connectivity2020 - 2022Examination of fMRI signal dependencies (coherence) between brain regions.
EEG activity2020 - 2022EEG activity: Event related potentials and spectral band power for different trial types
fMRI task performance2020 - 2022Reaction time and accuracy

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026