Clinical trial Recruiting at 1 site Interventional Ages 18 to 35

Using tDCS to improve emotional health in young adults with mild depressive symptoms

Official title: Utilizing Transcranial Direct Current Stimulation (tDCS) to Alleviate Subthreshold Depression Via Distinct Positive and Negative Emotion Pathways

Run by The University of Hong Kong · NCT07319143 · Data updated 2026-11-12

This study will test whether transcranial direct current stimulation (tDCS) can improve mood, motivation, and emotion regulation in 18–35-year-olds with subthreshold depression.

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Quick facts

Study typeInterventional
Ages18 Years to 35 Years
SexAll
Enrollment90 (estimated)
SponsorThe University of Hong Kong
Academic / other
Locations1 site (Hong Kong)
StatusRecruiting
StartedJanuary 8, 2026
Main results expectedSeptember 1, 2027
Study endsSeptember 1, 2027
Registry record updatedMay 4, 2026
Trial IDNCT07319143 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are 18–35-year-olds fluent in Cantonese or Mandarin, right-handed, with C-BDI-II scores ≥ 13, at least 9 years of education, and no major medical or psychiatric disorders or recent psychotropic medication use.

Probably not a fit

People with current or past major psychiatric or neurological disorders, recent psychotropic medication use, pregnancy, brain implants, other tDCS contraindications, or who cannot attend in-person sessions are unlikely to be eligible or to benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Young adults aged 18–35 with subthreshold depressive symptoms (C-BDI-II ≥ 13) are screened online and in person and then randomized to receive active tDCS targeted to either the left dorsolateral prefrontal cortex or the right ventrolateral prefrontal cortex, or to receive sham stimulation. Emotional function outcomes such as mood regulation, motivation, and positive/negative affect are compared across the three groups. Key eligibility requirements include fluency in Cantonese or Mandarin, right-handedness, minimum education, and absence of major medical or psychiatric disorders or recent psychotropic medication. The protocol uses noninvasive neuromodulation (tDCS) with standard safety exclusions for brain injury, implants, pregnancy, and recent neuromodulation exposure.

Why it matters

Potential benefit: If successful, tDCS could provide a non-drug, low-risk option to reduce depressive symptoms and improve emotion regulation in young adults with subthreshold depression.

How similar studies have gone: Previous tDCS studies have shown modest and mixed benefits for depressive symptoms and emotional regulation, but directly comparing left DLPFC versus right VLPFC stimulation for subthreshold depression is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 18-35 years
* Fluency in Cantonese or Mandarin
* Normal or corrected-to-normal vision and hearing
* IQ \> 75% Quantile in Raven's SPM
* At least 9 years of formal education
* Right-handedness

Exclusion Criteria:

* Past or current major physical illness or psychiatric disorders
* Use of psychotropic medication in the past 6 months
* Pregnancy (for women)
* Any condition that prevents safe tDCS use (e.g., brain injury, implants)
* Previous participation in neuromodulation in the past 3 months

Where it's running

  • The University of Hong Kong
    Hong Kong, Hong Kong
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.