- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07592559
tDCS and the Gaze Cueing Effect
May 11, 2026 updated by: Shan Gao, University of Electronic Science and Technology of China
Influence of Transcranial Direct Current Stimulation Applied to the Right Orbitofrontal Cortex on Gaze and Arrow Cueing Effects
This study employs transcranial direct current stimulation (tDCS) to investigate the role of the orbitofrontal cortex (OFC) in processing gaze and arrow cues.
Study Overview
Status
Completed
Conditions
Detailed Description
This study employs transcranial direct current stimulation (tDCS) to investigate the role of the orbitofrontal cortex (OFC) in processing gaze and arrow cues.To examine the distinct functions of the OFC in processing social versus non-social stimuli, participants were randomly assigned to one of three tDCS groups: anodal, cathodal, or sham.
Following stimulation, all participants completed a spatial cueing task involving both gaze and arrow cues.
Two stimulus onset asynchrony (SOA) conditions (200 ms and 600 ms) were implemented to investigate how timing modulates the processing of these cues within the rOFC.
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Sichuan
-
Chengdu, Sichuan, China, 611731
- School of Foreign Languages, University of Electronic Science and Technology of China
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- healthy subjects without past or current psychiatric or neurological disorders
Exclusion Criteria:
- history of head injury
- no implants in the head
- medical or psychiatric illness.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: anodal tDCS
anodal tDCS rOFC
|
use eye gaze images as cues
use arrow images as cues
The stimulus onset asynchrony (SOA) between the cue and the target was 200 ms.
The stimulus onset asynchrony (SOA) between the cue and the target was 600 ms.
The cue is spatially congruent with the target.
The cue is spatially incongruent with the target.
|
|
Experimental: cathodal tDCS
cathodal tDCS rOFC
|
use eye gaze images as cues
use arrow images as cues
The stimulus onset asynchrony (SOA) between the cue and the target was 200 ms.
The stimulus onset asynchrony (SOA) between the cue and the target was 600 ms.
The cue is spatially congruent with the target.
The cue is spatially incongruent with the target.
|
|
Sham Comparator: sham tDCS
sham tDCS rOFC
|
use eye gaze images as cues
use arrow images as cues
The stimulus onset asynchrony (SOA) between the cue and the target was 200 ms.
The stimulus onset asynchrony (SOA) between the cue and the target was 600 ms.
The cue is spatially congruent with the target.
The cue is spatially incongruent with the target.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reaction time to the judgment of the target location.
Time Frame: 1 hour
|
The primary analysis focused on the reaction times for judging the target location under each condition.
|
1 hour
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Magnitude of the cueing effect
Time Frame: 1 hour
|
This index is derived by subtracting the congruent reaction time from the incongruent reaction time to quantify the magnitude of the cueing effect.
|
1 hour
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 2, 2022
Primary Completion (Actual)
October 30, 2022
Study Completion (Actual)
December 8, 2022
Study Registration Dates
First Submitted
April 23, 2026
First Submitted That Met QC Criteria
May 11, 2026
First Posted (Actual)
May 18, 2026
Study Record Updates
Last Update Posted (Actual)
May 18, 2026
Last Update Submitted That Met QC Criteria
May 11, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UESTC-GazeLab-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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