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Идёт набор NCT07468279

Synchronization of Theta to Influence Memory

Без фазы С лечением Cognitive Control Memory

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Sham device, STARSTIM Device in-phase, STARSTIM Device anti-phase.
Кому может быть актуально
Состояния в реестре: Cognitive Control, Memory. Базовые параметры: 18 лет — 59 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Официальное название

Effects of Non-Invasive Brain Stimulation on Task Performance

Обзор

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

Вмешательства

  • Устройство Sham device
    Intervention which uses an inactive form of stimulation via electrodes on the scalp.
  • Устройство STARSTIM 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.
  • Устройство STARSTIM 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.

Первичные конечные точки

  • The Difference Between Incidental Memory of Faces on Error versus Correct Trials from Baseline to Post Brain Stimulation [Срок оценки: Baseline through study visit completion, a maximum of 3 hours]

Критерии участия

Критерии включения

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

Критерии исключения

  • 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 fillings).
  • 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.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Четверное слепое
Основная цель
Фундаментальное исследование

Центры проведения

США · 1 центр
  • Florida International University — Miami

Идентификаторы

NCT: NCT07468279 · IRB-25-0555

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗