Targeted tACS for anhedonia in older adults with depression
Official title: Efficacy and Mechanisms of Personalized tACS Targeting Anhedonia in Late-Life Depression
Run by Tianjin Anding Hospital · NCT07637773 · Data updated 2026-11-12
We’re testing personalized transcranial alternating current stimulation (tACS) to see if it improves anhedonia and depressive symptoms in people aged 60 and up with late-life depression.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 60 Years and up |
| Sex | All |
| Enrollment | 80 (estimated) |
| Sponsor | Tianjin Anding Hospital Academic / other |
| Locations | 1 site (Tianjin, Tianjin Municipality) |
| Status | Recruiting |
| Started | March 16, 2026 |
| Main results expected | December 31, 2027 |
| Study ends | December 31, 2027 |
| Registry record updated | June 10, 2026 |
| Trial ID | NCT07637773 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 60 years and older with major depressive disorder and significant anhedonia (HAMD-17 > 24).
✕Probably not a fit
Individuals with certain brain conditions, implants, or recent modulation therapies may not benefit from this approach.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to optimize individualized tACS treatment parameters for treating anhedonia in late-life depression. It uses randomized, double-blind, controlled trials to develop precise protocols guided by deep learning. The research will measure short-term (2 weeks) and longer-term (3 months) outcomes on depression and anhedonia with standard scales while monitoring safety. Multimodal data, including EEG and biomarkers, will help explain how tACS changes brain oscillations and neurotransmitter activity to ease anhedonia. The project seeks to establish a first-of-its-kind parameter system for personalized tACS in geriatric depression.
Why it matters
Potential benefit: If successful, patients may experience reduced anhedonia and depressive symptoms with a non-pharmacological, personalized brain stimulation approach.
How similar studies have gone: Previous non-personalized tACS work suggests potential for mood-related benefits, but personalized parameter optimization for anhedonia in late-life depression is novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * (1) Patients were interviewed using the Structured Clinical Interview for the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) - Clinical Version (SCID-5-CV) to confirm that they met the DSM-5 diagnostic criteria for "major depressive disorder"; (2) Age ≥ 60 years; gender not restricted; (3) Hamilton Depression Scale (HAMD)-17 score \> 24 Exclusion Criteria: \- (1) History of severe head trauma or serious neurological conditions such as epilepsy; (2) Any brain devices or implants, including cochlear implants and aneurysm clips; treatments such as transcranial direct current stimulation (tDCS). (3) Individuals who have undergone other physical modulation therapies within the past 8 weeks, including but not limited to non-convulsive electroconvulsive therapy, repetitive transcranial magnetic stimulation, and transcranial direct current stimulation.
Where it's running
-
Tianjin Anding Hospital
Tianjin, Tianjin Municipality, China Recruiting
Study contacts
- Study coordinator: Daliang Sun Da liang Sun, Doctor
- Email: 474929588@qq.com
- Phone: +86 88188876
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.