Efficacy and Safety Assessment of Temporal Interference Stimulation to Improve Bipolar Depression

Recruiting N/A Interventional Study
Bipolar Depression
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 45
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
160 (estimated)
Sponsor
First Affiliated Hospital of Zhejiang University · Other
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About This Trial

The aim of this study was to explore the efficacy and safety of temporal interference stimulation to improve bipolar depression, as well as to explore the corresponding neuroimaging mechanisms using magnetic resonance and electroencephalogram to provide novel intervention protocols and objective indicators of efficacy prediction for depressive episodes in bipolar disorder.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * right-handed, and have completed nine years of compulsory education; * Meet the diagnostic criteria for bipolar depression in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5); * ≥18 points on the Hamilton Depression Inventory (HAMD- 17); * ≤8 po…
Contacts

Shaohua Hu, PhD

0571-87232984

dorhushaohua@zju.edu.cn

CONTACT