- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04643340
Imaging During Subliminal Perception
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
Detailed Description
In this project, using healthy adults, the investigators have 2 aims:
- Apply electroencephalography (EEG) and fMRI before and after rt-fMRI neurofeedback during attention tasks to identify brain regions involved in subliminal and supraliminal perception.
- Apply functional connectivity analyses during these tasks.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Zürich, Switzerland
- University of Zurich
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
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
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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active group 1
This group will train the insular cortex by real-time fMRI
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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).
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active group 2
This group will train the visual cortex by real-time fMRI
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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
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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fMRI during supra-threshold and subliminal perception
Time Frame: 2020 - 2022
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2020 - 2022
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rt-fMRI activity
Time Frame: 2020 - 2022
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rt-fMRI activity: fMRI signal changes during repetitive real time fMRI based training
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2020 - 2022
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Functional connectivity
Time Frame: 2020 - 2022
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Examination of fMRI signal dependencies (coherence) between brain regions.
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2020 - 2022
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EEG activity
Time Frame: 2020 - 2022
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EEG activity: Event related potentials and spectral band power for different trial types
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2020 - 2022
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fMRI task performance
Time Frame: 2020 - 2022
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Reaction time and accuracy
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2020 - 2022
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Lars Michels, PhD, University Hospital, Zürich
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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