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Intervention study on attentional bias of negative emotional faces in patients with depression

Intervention study on attentional bias of negative emotional faces in patients with depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106683
Enrollment
Unknown
Registered
2025-07-28
Start date
2023-12-20
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Depressive disorder

Interventions

Group1:TMS intervention for sad face:Transcranial magnetic stimulation (TMS) was used to intervene the occipito-facial brain region with a figure 8 coil at a frequency of 10Hz and an intensity of 0.5s
Group2:TMS intervention forneutral face:Transcranial magnetic stimulation (TMS) was used to intervene the occipito-facial brain region with a figure 8 coil at a frequency of 10Hz and an intensity of 0
Group3: The intervention of TMS in control brain area for negative face:Transcranial magnetic stimulation (TMS) was used to intervene the occipito-facial brain region with a figure 8 coil at a frequen
Healthy control group:none

Sponsors

Peking University Sixth Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Meet the DSM-V clinical diagnostic criteria for depression; 2) Age: 18-60 years old, right-handed; Chinese speakers; 3) Obtain the patient's written informed consent; 4) Obtain the patient's written informed consent; 5) Normal vision or normal vision after correction; 6) Hamilton Depression Scale 17 items score > 17 7) Initial diagnosis or stable medication for more than 2 weeks Healthy persons must comply with items 2-5.

Exclusion criteria

Exclusion criteria: 1) Schizoaffective disorder, schizophrenia, mental retardation, generalized developmental disorder, delirium, dementia, memory impairment, or other cognitive impairment meeting the DSM-V diagnostic criteria; Those at high risk of suicide; Have epilepsy or a family history of epilepsy; 2) suffering from serious and unstable physical diseases; 3) Use of rTMS or MECT within 3 months before enrollment; 4) Contraindications for MRI scanning (the MRI safety review form needs to be completed when signing the informed consent form); 5) Difficult to cooperate with the completion of the assessment;

Design outcomes

Primary

MeasureTime frame
Fixation duration;Accuracy rate;Reaction time;

Countries

China

Contacts

Public ContactLin Lu

Peking University Sixth Hospital, Beijing, China

523823376@qq.com+86 136 0373 7632

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026