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Recruiting NCT07111169

NCT07111169 Neuromodulation and Attention Deficits in MDD

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Clinical Trial Summary
NCT ID NCT07111169
Status Recruiting
Phase
Sponsor University of Electronic Science and Technology of China
Condition Major Depression Disorder
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2024-01-01
Primary Completion 2028-12-30

Trial Parameters

Condition Major Depression Disorder
Sponsor University of Electronic Science and Technology of China
Study Type INTERVENTIONAL
Phase N/A
Enrollment 60
Sex ALL
Min Age 18 Years
Max Age 55 Years
Start Date 2024-01-01
Completion 2028-12-30
Interventions
intermittent theta burst stimulation (iTBS) intervention

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Brief Summary

Multimodal study (Behavior, TMS, EEG) combining a sham-controlled intermittent theta burst stimulation (iTBS) intervention with an additional-singleton task and EEG to evaluate whether left dorsolateral prefrontal cortex (DLPFC) stimulation enhances cognitive control and modulates maladaptive attention processes in MDD and whether the effects are influenced by neuronavigated versus manual (Beam F3 method) localization of the stimulation site.

Eligibility Criteria

Inclusion Criteria: * 18-55 years * Right-handed * Normal or corrected normal visual acuity * MDD: meet the proposed DSM-5 MDD criteria, unmedicated or stable medicated within the last one month. Healthy subjects without any past or present psychiatric or neurological disorders. Exclusion Criteria: * Diagnosis of other severe mental disorders, such as schizophrenia, bipolar disorder, neurodevelopmental disorder, etc. * high suicidal risk * Unnormal intellectual functioning, auditory impairments, * Have received neuromodulation, such as Modified Electroconvulsive Therapy (MECT), or any psychotherapy within the past 6 months. * Only for the active-iTBS group: have a contraindication to MRI scanning (e.g., metal implants, claustrophobia or other conditions that make them inappropriate for MRI scanning).

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