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Study identifier: NCT07319143 Synced from ClinicalTrials.gov · July 28, 2026
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The Effect of Transcranial Direct Current Stimulation (tDCS) in Improving Emotion Health

Condition: Subthreshold Depression · Positive Emotions · Negative Emotions  ·  Sponsor: The University of Hong Kong

PhaseNA
Planned participants90
Who can joinAll sexes, 18 Years to 35 Years
Healthy volunteersYes

About this study

The goal of this clinical trial is to investigate how transcranial direct current stimulation (tDCS) affects emotion functions in young adults aged 18-35 from the local community, including both male and female participants. The main question\[s\] it aims to answer are: * Does tDCS improve emotional functions, such as mood regulation and motivation, in individuals with subthreshold depression (StD)? * Can tDCS enhance emotional regulation compared to a sham stimulation (placebo)? Researchers will compare participants receiving tDCS on either the left dorsolateral prefrontal cortex (lDLPFC) or right ventrolateral prefrontal cortex (rVLPFC) with those receiving sham stimulation to see if tDCS has a stronger effect on emotional functions. Participants will: * Complete online and in-person screening to assess depressive symptoms using the Chinese version of the Beck Depression Inventory II (C-BDI-II) and be selected based on their depressive symptoms (C-BDI-II score ≥ 13). * Be randomly assigned to one of three groups: lDLPFC tDCS, rVLPFC tDCS, or Sham control group (1:1:1 ratio). * Receive 10 sessions of tDCS or Sham tDCS over 2 weeks, with each session lasting 20 minutes. * Complete assessments at baseline, post-intervention, 1-month follow-up, and 3-month follow-up, with each assessment lasting 2-2.5 hours. This includes questionnaires and perform emotional and cognitive tasks.

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

Talk to the study team

Associate Professor, Principle Investigator  ·  +852-3917-8927  ·  rshao@hku.hk

Always discuss trial participation with your own doctor first.

Locations (1)

The University of Hong KongHong Kong, Hong KongRecruiting

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Source record: clinicaltrials.gov/study/NCT07319143