Clinical trial Recruiting at 1 site Interventional Ages 60 and up

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 typeInterventional
Ages60 Years and up
SexAll
Enrollment80 (estimated)
SponsorTianjin Anding Hospital
Academic / other
Locations1 site (Tianjin, Tianjin Municipality)
StatusRecruiting
StartedMarch 16, 2026
Main results expectedDecember 31, 2027
Study endsDecember 31, 2027
Registry record updatedJune 10, 2026
Trial IDNCT07637773 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

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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.