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Synchronization of Theta to Influence Memory

Effects of Non-Invasive Brain Stimulation on Task Performance

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07468279
Acronym
STIM
Enrollment
90
Registered
2026-03-12
Start date
2026-03-13
Completion date
2031-01-01
Last updated
2026-08-27

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

Conditions

Cognitive Control, Memory

Brief summary

This study aims to clarify relations between brain oscillations and two cognitive functions: cognitive control and memory.

Interventions

DEVICESham device

Intervention which uses an inactive form of stimulation via electrodes on the scalp.

DEVICESTARSTIM Device in-phase

Intervention that uses the Starstim tES device to introduce transcranial alternating current stimulation (tACS) in the form of in-phase theta (\~3.5 to \~7.5 Hz) via electrodes on the scalp.

DEVICESTARSTIM Device anti-phase

Intervention that uses the Starstim tES device to introduce transcranial alternating current stimulation (tACS) in the form of anti-phase stimulation via electrodes on the scalp.

Sponsors

Florida International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 59 Years
Healthy volunteers
Yes

Inclusion criteria

* 18 years and older * Fluent in English * Normal or corrected-to-normal vision * Willing to be photographed

Exclusion criteria

* Must not have ever had an injury to the head that's caused you to be knocked out for a period of time (e.g., from a fall, blow to the head, road traffic accident). * Must not have an uncorrected vision or physical disability that interferes with your ability to see stimuli presented briefly on a computer screen or click a mouse button rapidly. * Must not have a history of epilepsy, convulsions, or seizures (except childhood febrile seizures). * Must not have a history of fainting or syncope. * For female participants, they must not be pregnant and/or must not think they might be pregnant. * Must not have skin problems like eczema, dermatitis, or open wounds on the scalp. * Must not have had prior brain surgery. * Must not have any metal located in the head/neck (except for dental work i.e., braces, permanent retainers, etc.) * Must not have any devices or other implants located in/near their head. This includes cochlear implants and aneurysm clips, cardiac pacemaker, or any other implanted electronic device. * Must not have a current (active) alcohol or substance use disorder, must have no recent history of withdrawal symptoms, and must be able to safely abstain from alcohol and non-prescribed/illicit drugs for at least 24 hours before the session. * Must not have any alcohol on the day of the session, must limit alcohol consumption to no more than 2 drinks (if legally permitted) in the prior 24 hours, and must not use any non-prescribed or illicit drugs in the 24 hours before the session. * Must not be sick with a fever, sleep-deprived, or feel dizzy, unwell, or intoxicated. * Must also have eaten and had fluids but not have consumed more caffeine than they typically consume. * Must not be taking anticonvulsant/anti-epileptic drugs or have ever taken them within their lifetime. * Must not be taking benzodiazepines or have taken them within the past 3 months. * Must not have had a recent change (start, stop, dose change) for any psychiatric/psychotropic medications within the past 3 months. * Must not be taking Bupropion (Wellbutrin, Zyban), Tricyclic antidepressants (e.g., amitriptyline, imipramine, clomipramine, etc.), Antipsychotics (clozapine; chlorpromazine, haloperidol, etc.), or Tramadol or have taken them within the past 3 months. * Must not have experienced cardiac problems, fibrillation, or have taken medications associated with cardiac conditions within the past 3 months. * Must not meet the diagnostic threshold for Autism Spectrum Disorder, Intellectual Disability, or Psychotic Disorders.

Design outcomes

Primary

MeasureTime frameDescription
The Difference Between Incidental Memory of Faces on Error versus Correct Trials from Baseline to Post Brain StimulationBaseline through study visit completion, a maximum of 3 hoursThe hit rate for faces that appeared on error trials minus the hit rate for faces that appeared on correct trials.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 28, 2026