Effects of Transcranial Oscillatory Direct Current Stimulation on the Functions of Cerebral Cortex in Healthy Subjects

NCT ID: NCT06076044

Last Updated: 2024-02-23

Study Results

Results pending

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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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-06-01

Study Completion Date

2024-03-15

Brief Summary

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To investigate the effect of transcranial oscillatory direct current stimulation on functions of cerebral cortex (cortical excitability and frequency of eeg) in healthy subjects

Detailed Description

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Conditions

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Transcranial Direct Current Stimulation Motor Evoked Potential Healthy Subjects

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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healthy subjects

healthy male subjects aged 20-30 years

Group Type EXPERIMENTAL

toDCS 2mA 1Hz

Intervention Type DEVICE

The subgroup treated by transcranial oscillatory direct current stimulation of 2mA and 1Hz.

toDCS 2mA 10Hz

Intervention Type DEVICE

The subgroup treated by transcranial oscillatory direct current stimulation of 2mA and 10Hz.

tDCS 1mA

Intervention Type DEVICE

The subgroup treated by transcranial direct current stimulation of 1mA.

sham

Intervention Type DEVICE

The subgroup treated by sham stimulation.

Interventions

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toDCS 2mA 1Hz

The subgroup treated by transcranial oscillatory direct current stimulation of 2mA and 1Hz.

Intervention Type DEVICE

toDCS 2mA 10Hz

The subgroup treated by transcranial oscillatory direct current stimulation of 2mA and 10Hz.

Intervention Type DEVICE

tDCS 1mA

The subgroup treated by transcranial direct current stimulation of 1mA.

Intervention Type DEVICE

sham

The subgroup treated by sham stimulation.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Healthy male
* Age ranges from 20 to 30 years old
* No history of neurological or psychiatric diseases, no history of chronic illness
* No positive results were found in the examination of the nervous system
* All right-handed according to Edinburgh Handedness Inventory
* The subjects voluntarily participated in this study and signed an informed consent form

Exclusion Criteria

* Individuals with severe illnesses
* Previous history of brain surgery or epilepsy
* Individuals who experience changes in physical condition during the experiment
* Individuals with metal implants, such as pacemakers, DBS therapists, stents, etc
* Alcoholics
Minimum Eligible Age

20 Years

Maximum Eligible Age

30 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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The First Hospital of Hebei Medical University

OTHER

Sponsor Role lead

Responsible Party

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Yuan Xing

Attending, Department of Neurology, Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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the First Hospital of Hebei Medical University

Shijiazhuang, Hebei, China

Site Status RECRUITING

Countries

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China

Central Contacts

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Yuan Xing, PhD, MD

Role: CONTACT

+8618633888925

Nan Zhang, PhD, MD

Role: CONTACT

+8618633888974

Facility Contacts

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Yuan Xing, PhD, MD

Role: primary

+8618633888925

Nan Zhang, PhD, MD

Role: backup

+8618633888974

Other Identifiers

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FirstHebei

Identifier Type: -

Identifier Source: org_study_id

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