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Clinical Trial Summary

The purpose of this study is to assess the mechanisms of the effect of transcranial direct current stimulation (tDCS) in alleviating subthreshold depressive symptoms in young individuals, and individualized outcome prediction is carried out.


Clinical Trial Description

After being informed about the study and potential risks, all participants providing written informed consent will undergo screening to determine eligibility for study entry. On day 0, participants who meet the eligibility requirements will be randomized in a double-blind manner (participant and investigator) in a 1:1:1 ratio to receive tDCS targeting the left dorsolateral prefrontal cortex (lDLPFC), tDCS targeting the right ventrolateral prefrontal cortex (rVLPFC), or Sham stimulation (10 sessions in 2 weeks). At baseline, after 2 weeks of stimulation, and at follow-up after 1 month and 3 months, participants will be assessed for brain network function, depressive symptoms, emotional status and social interactions. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06294184
Study type Interventional
Source Guangzhou Psychiatric Hospital
Contact Kangguang Lin, M.D;Ph.D
Phone 86-02081268189
Email linkangguang@163.com
Status Recruiting
Phase N/A
Start date November 1, 2023
Completion date December 2024

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