NCT07287878

Brief Summary

Major depressive disorder (MDD) is a mood disorder characterized primarily by low mood, diminished interest, and reduced energy. Traditional views considered depression a non-degenerative condition; however, recent epidemiological studies have revealed its significant association with impaired social functioning. Data indicate that 59.3% of patients with depression experience social dysfunction of varying severity \[1\], particularly manifesting as difficulties in social interaction and relationship maintenance \[2\]. Therefore, investigating the mechanisms underlying social dysfunction is of great importance for promoting functional recovery in MDD, and dysfunction within the social reward system may represent a core factor, though the specific neural mechanisms remain unclear. The ultimate goal of understanding the neural mechanisms underlying social reward impairment in depressed patients is to improve therapeutic outcomes. Temporal Interference (TI) stimulation, as a non-invasive deep brain stimulation technique, utilizes high-frequency current differentials to generate low-frequency amplitude-modulated electric fields, enabling precise targeting of deep brain regions. This study employs multimodal assessment methods-such as functional magnetic resonance imaging (fMRI), electroencephalography (EEG), and specific cognitive-behavioral tasks-combined with TI stimulation to observe immediate changes in functional connectivity, neural activity, and related cognitive functions (e.g., decision-making, memory) across participant groups. The research aims to elucidate the roles of the parahippocampal gyrus, orbitofrontal cortex, and striatum in social reward impairment in depression, and to explore circuit-based intervention targets, thereby providing novel strategies for the recovery of social functioning in MDD.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for not_applicable depression

Timeline
2mo left

Started Nov 2025

Shorter than P25 for not_applicable depression

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress73%
Nov 2025Jul 2026

Study Start

First participant enrolled

November 15, 2025

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

November 16, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

December 17, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 10, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 10, 2026

Last Updated

December 24, 2025

Status Verified

November 1, 2025

Enrollment Period

6 months

First QC Date

November 16, 2025

Last Update Submit

December 17, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • Change in Hamilton Depression Rating Scale (HAMD) Score

    The HAMD is a clinical depression assessment and consists of 17 items with a total score range from 0 to 54.A higher score indicates a worse outcome.

    baseline and immediately after the intervention

  • Change in The Positive and Negative Affect Schedule (PANAS) Score

    The Positive and Negative Affect Schedule (PANAS) is an assessment of participants' immediate affective states and consists of 20 items divided into two subscales (10 items for Positive Affect and 10 items for Negative Affect), with each item rated on a 5-point scale; higher scores on the Positive Affect subscale indicate more positive emotional states, while higher scores on the Negative Affect subscale indicate more negative emotional states.

    Baseline and immediately after the intervention

Secondary Outcomes (1)

  • MRI measures

    Baseline and immediately after the intervention

Study Arms (4)

orbitofrontal cortex

EXPERIMENTAL
Device: Temporal Interference Simulation(TIS)

parahippocampal gyrus

EXPERIMENTAL
Device: Temporal Interference Simulation(TIS)

striatum

EXPERIMENTAL
Device: Temporal Interference Simulation(TIS)

sham

SHAM COMPARATOR
Device: Temporal Interference Stimulation(TIS)

Interventions

the total stimulation duration was 20 minutes, including a 40-second current ramp-up at the beginning and a 40-second ramp-down at the end.

orbitofrontal cortexparahippocampal gyrusstriatum

Sham stimulation has only 40 seconds of current ramping-up and ramping-down at the beginning and end of the stimulation to simulate the sensation of actual stimulation.

sham

Eligibility Criteria

Age16 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • years old;
  • Meeting with the criteria of major depressive disorder in the Diagnostic and Statistical Manual of Mental Disorders (DSM)-5;
  • Scored 20 or higher on the Hamilton's Depression Scale with 24 items (HAMD-24);
  • With enough audio-visual ability and comprehensive ability to accomplish the visits;
  • Be necessary and suitable to accept the treatment of antidepressants;
  • Scored less than 14 on Hamilton's Anxiety Scale (HAMA) and scored less than 14 on the Hypomania Symptom Checklist-32 (HCL-32);
  • With 2 or more atypical symptoms including significant weight gain or increase in appetite, hypersomnia, leaden paralysis, and a long-standing pattern of interpersonal rejection sensitivity that results in significant social or occupational impairment.

You may not qualify if:

  • Severe medical or neurological problems;
  • Previous mania or hypomania episodes;
  • Female patients who are pregnant, planning to be pregnant or breastfeeding;
  • Actively suicide ascertained by research psychiatrist or 3rd item of HAMD scored≥3(suicidality);
  • Had ECT, MECT or rTMS in the past 6 months;
  • Experienced severe personality disorder, mental retardation, anorexia/ bulimia nervosa.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shanghai Mental Health Center

Shanghai, China, China

RECRUITING

MeSH Terms

Conditions

Depression

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Central Study Contacts

daihui Peng, MD. PhD.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, CARE PROVIDER
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 16, 2025

First Posted

December 17, 2025

Study Start

November 15, 2025

Primary Completion (Estimated)

May 10, 2026

Study Completion (Estimated)

July 10, 2026

Last Updated

December 24, 2025

Record last verified: 2025-11

Locations