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Study identifier: NCT06878326 Synced from ClinicalTrials.gov · July 29, 2026
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Resting-State Functional Connectivity as a Predictor of tDCS Effects in Adolescents With Autism Spectrum Disorder

Condition: Autism Spectrum Disorder (ASD) · Transcranial Direct Current Stimulation (tDCS) · Electroencephalography  ·  Sponsor: The Hong Kong Polytechnic University

PhaseNA
Planned participants90
Who can joinAll sexes, 12 Years to 22 Years
Healthy volunteersNo

About this study

Background: Transcranial Direct Current Stimulation (tDCS) is a form of non-invasive brain stimulation that has aroused increased interests in the past decade. Not only that it is transient with little side-effects, and can be well-tolerated by children, it is also affordable and readily accessible, making it an appealing treatment option for autism spectrum disorder (ASD). Objective: (1) To evaluate the therapeutic effects of tDCS on improving cognitive function in patients with ASD, (2) to better understand the neural mechanisms underlying the neuromodulation effects of tDCS in patients with ASD, and (3) to determine whether resting-state functional connectivity measures can predict the therapeutic effects of active tDCS in individuals with ASD. Methods: To assess the therapeutic effects and neural mechanisms of tDCS, 90 adolescents with ASD (age 12-22 years) will receive three stimulation conditions: cathodal tDCS of the left DLPFC, anodal tDCS of the left DLPFC and sham-tDCS with at least a week apart each time. During the active tDCS or sham-tDCS condition, the participants will be administered a computerized test battery (Cambridge Neuropsychological Test Automated Battery, CANTAB®) to evaluate their cognitive function. EEG before and after the tDCS to evaluate the tDCS-induced alteration in their neural activity and functional connectivity. Hypothesis: Drawing together the different evidence linking ASD with cortical hyper-excitability and disordered neural connecti…

This description comes directly from the study's public registry record.

Talk to the study team

Yvonne Han, PhD  ·  +852 2766 7578  ·  yvonne.han@polyu.edu.hk

Always discuss trial participation with your own doctor first.

Locations (1)

The Hong Kong Polytechnic UniversityHung Hom, Kowloon, Hong KongRecruiting

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Source record: clinicaltrials.gov/study/NCT06878326