NCT07625566

Brief Summary

Background: Visuospatial attention enables individuals to detect and process relevant stimuli efficiently. The posterior parietal cortex (PPC), a core hub of the dorsal attention network, exerts top-down control over visual scanning and is closely linked to alpha-band oscillations (8-13 Hz), which index attentional allocation and inhibition of distractors. Transcranial direct current stimulation (tDCS) offers a noninvasive method to alter cortical excitability transiently, but evidence for its effects on PPC-mediated attention and alpha power remains mixed. Objective: This randomized, single-blind trial examined whether anodal tDCS over the left PPC modulates visuospatial attention and resting-state alpha power in young adults, and whether EEG changes predict behavioral performance. Method: Thirty-two healthy participants (18-40 years) were randomized to anodal (2 mA, 20 min; n=15) or sham (n=17) stimulation. Cancellation Test performance and resting-state EEG were assessed pre- and post-stimulation. EEG analyses focused on artifact-free alpha power; regression models probed associations between neural and behavioral changes.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
32

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2021

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2021

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2021

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2021

Completed
4.6 years until next milestone

First Submitted

Initial submission to the registry

May 22, 2026

Completed
13 days until next milestone

First Posted

Study publicly available on registry

June 4, 2026

Completed
Last Updated

June 4, 2026

Status Verified

May 1, 2026

Enrollment Period

5 months

First QC Date

May 22, 2026

Last Update Submit

June 3, 2026

Conditions

Keywords

tDCSposterior parietal cortexvisuospatial attentionEEG alpha oscillations

Outcome Measures

Primary Outcomes (2)

  • EEG recording and power in alpha band

    EEG recordings were acquired in a semi-dark, electrically shielded Faraday room using a BrainAmp 32-Channel DC System (Brain Products, Munich, Germany). Signals were sampled at 500 Hz with a 0.01-250 Hz bandpass filter and recorded using BrainVision Recorder software. A 32-channel Ag/AgCl electrode cap (Easycap) was positioned according to the international 10-20 system. Resting-state EEG data were collected for 4 minutes with eyes open and 4 minutes with eyes closed. Numerical evaluation of artifact-free EEG data for power density calculation is performed using Fast Fourier Transform (FFT) with 0.5 Hz frequency resolution, and alpha (8-13 Hz) bands were calculated and then averaged over these power spectrum values. The amplitude values, measured from peak to peak, were recorded for each individual, and the necessary data for statistical analysis were collected.

    Before and immediately after applying tDCS

  • Cancellation Test

    The Cancellation Test is one of the most widely used tools for assessing visuospatial attention. IT consists of four subtests arranged on A4-sized sheets. Each subtest includes 60 target stimuli distributed among 300 total stimuli. For each subtest, separate scores are calculated for the right and left sides, including the number of correctly marked targets (IT1), omitted targets (IT2), incorrectly marked letters/shapes (IT3), total error score (IT4), and scanning time (IT5). The total error score is calculated as the sum of omitted targets and incorrectly marked letters/shapes. Achieving a high score (i.e., a high number of correctly marked targets and a low number of errors) and a short completion time (time score) indicate better performance. İn the present study, the paper-and-pencil version of the Cancellation Test was chosen to reliably assess visuospatial attention and subtle tDCS-induced changes.

    Before and immediately after applying tDCS

Study Arms (2)

Anodal tDCS Group

EXPERIMENTAL
Device: Anodal tDCS

Sham tDCS Group

SHAM COMPARATOR
Device: Sham tDCS

Interventions

Anodal tDCS Protocol: In the Anodal tDCS participant group, a direct current of 2 mA was applied for 20 minutes in accordance with the safety guidelines. To provide cortical stimulation, the superficial anodal electrode of the device was placed on the P3 region (left PPC), which is located in the left superior parietal lobe, corresponds to Brodmann area (BA) 40, and is associated with the dorsal visual pathway according to the international 10-20 EEG system. The reference electrode was placed on the contralateral (opposite) shoulder.

Anodal tDCS Group
Sham tDCSDEVICE

Sham tDCS Protocol: The anode superficial electrode of the device was placed on the P3 region (left PPC), located in the left superior parietal lobe, corresponding to Brodmann area (BA) 40, and associated with the dorsal visual pathway according to the international 10-20 EEG system. The reference electrode was placed on the contralateral (opposite) shoulder. In the Sham tDCS group, a single 20-minute sham session was administered over the left posterior parietal cortex (P3) without delivering current, in accordance with the safety guidelines.

Sham tDCS Group

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Age between 18 and 40 years
  • Score of 21 or higher on the Montreal Cognitive Assessment Scale (MoCA)

You may not qualify if:

  • History of neurological or psychiatric illness
  • Uncorrected visual impairments
  • MoCA score of 21 or lower
  • Use of medications affecting cortical excitability
  • History of seizures or epilepsy
  • Presence of intracranial metal objects, implanted stimulating devices, or pacemakers

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istanbul Medipol University

Beykoz, İ̇stanbul, 34820, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Transcranial Direct Current Stimulation

Intervention Hierarchy (Ancestors)

Electric Stimulation TherapyTherapeuticsConvulsive TherapyPsychiatric Somatic TherapiesBehavioral Disciplines and ActivitiesElectroshockPsychological Techniques

Study Officials

  • Mevhibe Sarıcaoğlu, PhD

    Medipol University

    STUDY CHAIR
  • Miray Budak, PhD

    Rutgers University-Newark

    STUDY DIRECTOR
  • Fatma Aydın, MsC

    Medipol University

    STUDY CHAIR
  • Lütfü Hanoğlu, Professor

    Medipol University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
lecturer

Study Record Dates

First Submitted

May 22, 2026

First Posted

June 4, 2026

Study Start

February 1, 2021

Primary Completion

July 1, 2021

Study Completion

November 1, 2021

Last Updated

June 4, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Locations