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Exploring the augmentative effects and mechanisms of integrating computerized cognitive training with transcranial magnetic stimulation in late-life depression: a proof-of-concept randomized controlled trial

Exploring the augmentative effects and mechanisms of integrating computerized cognitive training with transcranial magnetic stimulation in late-life depression: a proof-of-concept randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098068
Enrollment
Unknown
Registered
2025-03-03
Start date
2025-03-03
Completion date
Unknown
Last updated
2025-03-10

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

Conditions

Depression

Interventions

Experimental group:Active rTMS + Active CCT
Control group:Active rTMS + Sham CCT

Sponsors

The Chinese University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to 75 Years

Inclusion criteria

Inclusion criteria: Ethnic Chinese; aged 55 to 75 years; right-handed; living at home; having a primary diagnosis of major depressive disorder (single or recurrent episodes without psychotic features) based on DSM-5 criteria; current episode scoring >17 in the Hong Kong Chinese version of the 17-item Hamilton Rating Scale for Depression (HAM-D), with cognitive symptoms [Item 8 in HAM-D (slowness of thought and speech, impaired ability to concentrate) scoring =2]; not responding to an adequate dose of an antidepressant; and having received a stable antidepressant regimen for at least 4 weeks before joining this trial.

Exclusion criteria

Exclusion criteria: Alcohol or substance abuse; bipolar disorder; any psychotic disorder or current psychotic symptoms; dementia; active suicidal ideation; anxiety disorder; personality disorder; mental disorder due to organic cause; neurological disorders (Parkinson’s disease, stroke, brain tumor); and unstable physical illness. Individuals identified with these conditions will be excluded and referred to the Hospital Authority for further management. Other exclusion criteria are: history of seizure or epilepsy; contraindications to magnetic resonance imaging (MRI); metallic implants in cephalic region (including aneurysm clips, shuts, stimulators, cochlear implant, or electrodes); history of receiving non-invasive brain stimulation (TMS, tDCS, tACS, etc.), electroconvulsive therapy, cognitive training, or psychological intervention in the past 6 months; refusing blood taking or MRI; or having language barrier or communication impairments (poor vision and hearing despite correction).

Design outcomes

Primary

MeasureTime frame
HAM-D score;

Secondary

MeasureTime frame
Mood;Cognition;Level of functioning;Functional brain network;Cortical excitability;Serum BDNF level;

Countries

China

Contacts

Public ContactAllen Ting Chun Lee

The Chinese University of Hong Kong

allenlee@cuhk.edu.hk+852 2607 6031

Outcome results

None listed

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