Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
70 participants
INTERVENTIONAL
2021-02-01
2023-12-04
Brief Summary
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The investigators of this project would like to use these techniques to study the brain signals, while healthy participants are making the decisions choosing between 2 rewards, e.g., 2 food items. Participants who have depression show different behavior while performing decision-making tasks and the investigation of processes that underlie them will lead to a better understanding of this disease.
Furthermore, there is another category of tools, which help to study the brain. This category includes electrical stimulation, which mimics the electrical pattern that brain cells elicit. Application of external electrical stimulation can enhance this pattern or disrupt it and this process will affect the behavior of a person. Recent investigations have led to the development of a new stimulation technique that allows targeting deep brain regions. The investigators of this project want to apply this method to change the performance of healthy participants in the tasks on decision-making. If this experiment is successful, then stimulation can be used as a therapy for participants with depression.
Detailed Description
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Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
The sequence of sham/placebo and active stimulation will be randomized.
BASIC_SCIENCE
NONE
Study Groups
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TI stimulation
Temporal interference (TI) stimulation is a type of low-intensity transcranial electrical stimulation with alternating current (tACS). In case of TI stimulation, 2 electric fields in kHz range are delivered to 4 electrodes, which are placed on the surface of the skull, to modulate neural oscillations.
TI transcranial electrical stimulation
Participants will undergo transcranial electrical stimulation, which will be delivered with low current amplitudes (\<= 2 mA) established with international safety guidelines for electrical stimulation. Threshold for the current amplitude will be established by participants themselves, such that they cannot distinguish when stimulation is applied and not applied.
Duration of stimulation will not last longer than 30 minutes.
Interventions
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TI transcranial electrical stimulation
Participants will undergo transcranial electrical stimulation, which will be delivered with low current amplitudes (\<= 2 mA) established with international safety guidelines for electrical stimulation. Threshold for the current amplitude will be established by participants themselves, such that they cannot distinguish when stimulation is applied and not applied.
Duration of stimulation will not last longer than 30 minutes.
Eligibility Criteria
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Inclusion Criteria
* Age 18-40 years
* Normal physical and mental status (i.e. no neurological, musculoskeletal, neuromuscular, cognitive, or psychiatric disorders)
* If a participant already took part in the experiment with the same decision-making task
Exclusion Criteria
* epilepsy
* head traumas
* implants (cochlear, neurostimulators, cardiac pacemakers, medication infusion device)
* metal in the brain or skull
* work in the metal industry
* scars or inflammations on the regions, where the stimulation electrodes are placed
* administration of antipsychotic or anti-epileptic medication
* hearing problems or ringing in the ears
* syncope or fainting spells in the last 5 years
* severe side-effects after transcranial magnetic stimulation (TMS) or electrical stimulation if participant underwent it before
* pregnancy
* claustrophobia
* history of brain surgery
* family member that suffers from epilepsy
* suffering from medication abuse for more than a year or drug intake
* taking medications for medical reasons for more than a month
* receiving of depot injections
* one or more of the following materials in the body: metallic objects (e.g., dental implants, a metallic splinter in the eye, but not braces); wire, pacemaker or implanted defibrillator; artificial heart valves; vascular grafts; bio-stimulator or nerve stimulator; aneurysm or intracranial clip; cochlear implant; other prostheses or orthoses; implanted medication pump (insulin or pain pump); medicated patch (e.g., nitro-patch, pain patch, nicotine patch, hormone patch, motion sickness patch); other implants; tattoo or jewelry
* history of any of these illnesses: brain thrombosis, stroke, traumatic brain injury, meningitis, heart attack, prolonged loss of consciousness, migraine, epilepsy
18 Years
40 Years
ALL
Yes
Sponsors
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Swiss Federal Institute of Technology
OTHER
Responsible Party
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Rafael Polania
Principal Investigator
Principal Investigators
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Rafael Polania, PhD
Role: PRINCIPAL_INVESTIGATOR
ETH Zürich
Locations
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ETH Zurich
Zurich, Schweiz, Switzerland
Countries
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Other Identifiers
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TI_Reward
Identifier Type: -
Identifier Source: org_study_id