Imaging During Subliminal Perception

June 12, 2023 updated by: University of Zurich

Functional Imaging During Subliminal Perception

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.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

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.

Study Type

Observational

Enrollment (Actual)

70

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Zürich, Switzerland
        • University of Zurich

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Healthy adults

Description

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)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
active group 1
This group will train the insular cortex by real-time fMRI
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).
active group 2
This group will train the visual cortex by real-time fMRI
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).
sham
This group will only train the insula by a particular strategy

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
fMRI during supra-threshold and subliminal perception
Time Frame: 2020 - 2022
2020 - 2022
rt-fMRI activity
Time Frame: 2020 - 2022
rt-fMRI activity: fMRI signal changes during repetitive real time fMRI based training
2020 - 2022

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Functional connectivity
Time Frame: 2020 - 2022
Examination of fMRI signal dependencies (coherence) between brain regions.
2020 - 2022
EEG activity
Time Frame: 2020 - 2022
EEG activity: Event related potentials and spectral band power for different trial types
2020 - 2022
fMRI task performance
Time Frame: 2020 - 2022
Reaction time and accuracy
2020 - 2022

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Lars Michels, PhD, University Hospital, Zürich

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 15, 2020

Primary Completion (Actual)

December 1, 2021

Study Completion (Actual)

December 1, 2022

Study Registration Dates

First Submitted

November 16, 2020

First Submitted That Met QC Criteria

November 24, 2020

First Posted (Actual)

November 25, 2020

Study Record Updates

Last Update Posted (Actual)

June 13, 2023

Last Update Submitted That Met QC Criteria

June 12, 2023

Last Verified

June 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 2017-00483

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

Raw imaging data can be shared with other groups (outside of the USZ), e.g. for replication purpose.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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