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Effect of High-Definition Transcranial Direct Current Stimulation (HD-tDCS) on Attentional Control: an fMRI Study on Healthy Participants

U

University of Tehran

Status

Enrolling

Conditions

Healthy Volunteers

Treatments

Device: Active High-Definition Transcranial Direct Current Stimulation (HD-tDCS)
Device: Sham High-Definition Transcranial Direct Current Stimulation (HD-tDCS)

Study type

Interventional

Funder types

Other

Identifiers

NCT05613790
511098020

Details and patient eligibility

About

In a randomized, triple-blind, sham-controlled clinical trial, we will assess the effect of a single session frontal cortex High-Definition transcranial Direct Current Stimulation (HD-tDCS) on brain activity and functional connectivity underlying the behavioral change in attentional control in healthy participants. Participants will be recruited after meeting the inclusion criteria and will be randomly assigned to active or sham stimulation groups. All participants will undergo resting-state functional Magnetic Resonance Imaging (rsfMRI) scan and perform an Attention Network Test (ANT) in a functional Magnetic Resonance Imaging (fMRI) scanner before and after receiving a single session of active or sham HD-tDCS.

Enrollment

24 estimated patients

Sex

All

Ages

20 to 39 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Right-handed healthy adults
  • Age range 20-39 years
  • Normal or corrected-to-normal vision
  • Willing and capable of following study protocol requirements given in the informed consent

Exclusion criteria

  • Psychiatric conditions (e.g., depression and generalized anxiety disorder, etc.)
  • Medical illness or neurological disorder (e.g., cardiovascular illness, anemia, respiratory illness, neurological illness, seizure, etc.)
  • Current abuse of drugs or alcohol
  • Any conditions that prevent undergoing an fMRI scan or tDCS stimulation according to the fMRI and tDCS safety checklists

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

24 participants in 2 patient groups

Active HD-tDCS
Experimental group
Description:
Participants in the active arm will receive 20 min of real High-Definition transcranial direct current stimulation. Additional ramp-up and ramp-down phases at the beginning and the end of stimulation will last for 30 s.
Treatment:
Device: Active High-Definition Transcranial Direct Current Stimulation (HD-tDCS)
Sham HD-tDCS
Experimental group
Description:
During the sham session, the montage will be identical, however, the current amplitude will ramp up for 30 seconds, and for the remaining stimulation time, the current flow will terminate and will be kept to zero. Ramp-down phase at the end of stimulation will last for 30 s.
Treatment:
Device: Sham High-Definition Transcranial Direct Current Stimulation (HD-tDCS)

Trial contacts and locations

1

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Central trial contact

Faculty of Psychology

Data sourced from clinicaltrials.gov

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