Synchronization of Theta to Influence Memory

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-59
SponsorFlorida International University

About this trial

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

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

18 years and older

Fluent in English

Normal or corrected-to-normal vision

Willing to be photographed

Disqualifiers

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.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Sham device

    Device

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

  • STARSTIM Device in-phase

    Device

    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.

  • STARSTIM Device anti-phase

    Device

    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.

Treatment groups

90 Participants
are divided into 3 treatment groups
Group A: Sham StimulationSham comparator 1 intervention
Group B: STARSTIM device treatment (in-phase theta)Experimental treatment 1 intervention
Group C: STARSTIM device treatment (anti-phase stimulation)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

The Difference Between Incidental Memory of Faces on Error versus Correct Trials from Baseline to Post Brain Stimulation

The hit rate for faces that appeared on error trials minus the hit rate for faces that appeared on correct trials.

Time frame
Baseline through study visit completion, a maximum of 3 hours

Secondary outcomes

Other outcomes

Sponsors and contacts

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