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Non-Invasive Brain Stimulation

Effect of Conventional Transcranial Direct Current Stimulation (c-tDCS) and High-definition Transcranial Direct Current Stimulation (HD-tDCS) on the Prefrontal Cortex

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04318522
Enrollment
40
Registered
2020-03-24
Start date
2019-06-28
Completion date
2020-12-31
Last updated
2020-03-24

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

Conditions

Stroke

Brief summary

The study focusses on utilizing neuroimaging modalities, including Electroencephalography (EEG) and Functional Magnetic Resonance Imaging (fMRI) to study the impact of non-invasive brain stimulation on the prefrontal cortex during a cognitive task.

Detailed description

In this study, a total of 40 subjects will be randomly assigned to 2 groups i.e. experimental and sham. Conventional transcranial direct current stimulation (c-tDCS) and high-definition transcranial direct current stimulation (HD-tDCS) will be used to stimulate the prefrontal cortex of the brain. EEG and fMRI will be collected before, during and after stimulation to understand the impact of stimulation on brain dynamics. The investigators hypothesize that the stimulation of the prefrontal cortex will improve performance during cognitive tasks along with changes in the neural processing detected by neuroimaging modalities.

Interventions

Transcranial Direct Current Stimulation (tDCS) is a non-invasive brain stimulation device that can excite or inhibit the brain activity depending on the stimulation protocol. It has mainly two variants including conventional c-tDCS and High-Definition HD-tDCS.

Sponsors

Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Right Handedness, * Age \> 18

Exclusion criteria

* History of any other neurological disease, * Any psychological or psychiatric disease, * Significant visual or auditory impairments, * tDCS contraindications including implanted metallic or electronic devices, seizures or convulsions, and pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Reaction Time (RT)1 hourReaction time of the subject during a cognitive task would be a measure to assess changes in performance due to stimulation
Concentration Rate1 hourThe percentage of accurate responses during the cognitive task within the stipulated time will be calculated to see an impact on concentration after stimulation
Event related potential latency and amplitude1 hourChanges in latency and amplitude of event related potentials including P300 & N200 would be used as neural marker to understand cognitive processing in the brain.
Functional Magnetic Resonance Imaging (fMRI)1 hourChanges in fMRI connectivity

Countries

Hong Kong

Contacts

Primary ContactRaymond Tong, PhD
kytong@cuhk.edu.hk+852 3943 8454

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026