- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06740864
40 Hz Transcranial Alternating Current Stimulation for Inducing Gamma Oscillations
March 15, 2026 updated by: Mohammad Ali Salehinejad, The National Brain Mapping Laboratory (NBML)
Induction and Stabilization of Gamma Oscillations With 40 Hz Transcranial Alternating Current Stimulation in Healthy Elderly
This study aims to compare the efficacy of different 40 Hz tACS protocols in entraining gamma oscillations, which are linked to various cognitive functions and play a significant role in cognitive impairments like Alzheimer's disease.
Specifically, it examines the effects of 40 Hz tACS applied to frontal brain regions versus fronto-temporal regions on gamma oscillations and working memory in healthy elderly individuals.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
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
-
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Tehran, Iran
- Institute for Research in Fundamental Sciences
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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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- healthy elderly between 50-80 years of age
- normal or corrected to normal eye vision
- right-handed
- non-smokers
- at least 70 % accuracy in working memory training task
Exclusion Criteria:
- history of neurological or psychiatric disorders including seizures or epilepsy,
- Taking CNS, blood pressure and other medications
- having metal implants in the head and neck
- significant cognitive decline meassured by The Montreal Cognitive Assessment (MoCA)
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
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: 40 Hz prefrontal Transcranial alternating current stimulation
During prefrontal tACS, an alternating electrical current with a 1 milliamp peak-to-peak amplitude will be delivered, featuring a 15-second ramp-up at the start and a 15-second ramp-down at the end.
The stimulation duration is 20 minutes and four channels are used for delivering sinusoidal alternating currents to the head.
The alternating current was delivered to the prefrontal cortex bilaterally with the electrodes at F3 and F4 and the return electrodes were placed at the ipsilateral mastoids at TP9 and TP10 (international 10-20 EEG electrode placement system).
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Transcranial alternating current will be delivered utilizing a Starstim 8-channel constant current, battery-powered electric stimulator (Neuroelectrics, Barcelona, Spain).
Circular carbon rubber electrodes (2cm radius, 12,57 cm2) are used throughout the stimulation.
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|
Active Comparator: 40 Hz frontal-temporal Transcranial alternating current stimulation
During frontal-temporal tACS, an alternating electrical current with a personalized peak-to-peak stimulation intensity will be delivered, featuring a 15-second ramp-up at the start and a 15-second ramp-down at the end.
The stimulation duration is 20 minutes and four channels are used for delivering sinusoidal alternating currents to the head.
The alternating current was delivered to the prefrontal and temporal cortices with the active electrodes at AF3-T7 and the return electrodes over AF4-T8 (according international 10-20 EEG electrode placement system).
|
Transcranial alternating current will be delivered utilizing a Starstim 8-channel constant current, battery-powered electric stimulator (Neuroelectrics, Barcelona, Spain).
Circular carbon rubber electrodes (2cm radius, 12,57 cm2) are used throughout the stimulation.
|
|
Sham Comparator: sham Transcranial alternating current stimulation
During sham tACS, an alternating artificial electrical current will be delivered, only ramping the current for 15 seconds up and 15 seconds down at the beginning and end of the stimulation respectively.
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Sham tACS will be applied by only ramping the current for 15 seconds up and 15 seconds down at the beginning and end of the stimulation respectively.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Working Memory behavioral performance
Time Frame: During procedure (20 minutes)
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Participants view a continuous sequence of alphabet letters, presented as stimuli in Arial font, size 120pt, on a tube screen positioned at 60cm eye distance.
The stimuli are shown with a time interval of two seconds between them.
The task consisted of six blocks with 70 stimuli, including 12 possible hit trials.
Participants were instructed to press the left key on a response box if the presented stimulus matched either the one presented one trial prior (1-Back) or three trials prior (3-Back).
In all other cases, participants press the right key.
The left button is pressed with the index finger, while the right button is pressed with the middle finger of the right hand, with buttons aligned horizontally.
The response condition varied by block, with three blocks for 3-Back and three for 1-Back, and the order was counterbalanced across participants and sessions.
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During procedure (20 minutes)
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electroencephalogram (EEG) oscillatory power
Time Frame: up to 2 hours after the intervention
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Change in the EEG power in the gamma band
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up to 2 hours after the intervention
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electroencephalogram (EEG) functional connectivity
Time Frame: up to 2 hours after the intervention
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Change in EEG functional connectivity, specifically global efficiency, coherence, and phase-locking value at gamma frequency
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up to 2 hours after the intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
electroencephalogram (EEG) oscillatory power
Time Frame: up to 2 hours after the intervention
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Change in the EEG power in alpha, delta, theta and beta bands
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up to 2 hours after the intervention
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
June 1, 2024
Primary Completion (Actual)
February 1, 2025
Study Completion (Actual)
June 1, 2025
Study Registration Dates
First Submitted
December 14, 2024
First Submitted That Met QC Criteria
December 14, 2024
First Posted (Actual)
December 18, 2024
Study Record Updates
Last Update Posted (Actual)
March 18, 2026
Last Update Submitted That Met QC Criteria
March 15, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Mental Disorders
- Neurocognitive Disorders
- Cognition Disorders
- Dementia
- Tauopathies
- Neurodegenerative Diseases
- Cognitive Dysfunction
- Alzheimer Disease
- Therapeutics
- Behavioral Disciplines and Activities
- Electric Stimulation Therapy
- Convulsive Therapy
- Psychiatric Somatic Therapies
- Electroshock
- Psychological Techniques
- Transcranial Direct Current Stimulation
Other Study ID Numbers
- IfADo_196_P3
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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