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Neural Mechanisms Underlying Temporal Interference Stimulation–Modulated Facial Emotion Processing Deficits in Major Depressive Disorder

Neural Mechanisms Underlying Temporal Interference Stimulation–Modulated Facial Emotion Processing Deficits in Major Depressive Disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126402
Enrollment
Unknown
Registered
2026-06-09
Start date
2026-06-30
Completion date
Unknown
Last updated
2026-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major Depressive Disorder

Interventions

Intervention group:All participants received the two stimulation protocols in a random order (with a 7-day washout period): (1) 10 Hz TIS targeting the left DLPFC, (2) 0 Hz TIS (sham control).

Sponsors

Tianjin Anding Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Meets DSM-5 criteria for Major Depressive Disorder (MDD); first or recurrent episode. 2.Score of >14 on the 17-item Hamilton Depression Rating Scale (HAMD-17). 3.Age between 18 and 65 years. 4.No restriction on sex; 5.Han Chinese ethnicity; 6.Educational level of junior high school or above; 7.Normal vision or corrected-to-normal vision; 8.Right-handed, with adequate auditory, verbal, reading, and comprehension abilities to complete experimental tasks; 9.Either medication-naïve or on stable antidepressants for =4 weeks with no changes during the study; 10.Patient and their legal guardian (if applicable) have read, understood, and signed the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Diagnosed with other DSM-5 psychiatric disorders (e.g., organic mental disorder, substance use disorder, schizophrenia). 2.Current severe neurological condition (e.g., stroke, epilepsy, delirium); 3.Received physical therapies (e.g., ECT, TMS, tDCS) within the past 30 days; 4.Pregnant or breastfeeding women; 5.Contraindications to transcranial electrical stimulation (e.g., metallic implants, history/family history of seizures). 6.Any other factor deemed unsuitable for participation by the research team.

Design outcomes

Primary

MeasureTime frame
Oxyhemoglobin (HbO) concentration;

Secondary

MeasureTime frame
Accuracy;Response Time;

Countries

China

Contacts

Public ContactShen Li

Tianjin Anding Hospital

lishen@tmu.edu.cn+86 137 5211 5075

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026