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Neuroimaging markers of cognitive control deficits in first-episode medication-naïve elderly patients with depression before and after antidepressant treatment

Neuroimaging markers of cognitive control deficits in first-episode medication-naïve elderly patients with depression before and after antidepressant treatment

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600129731
Enrollment
Unknown
Registered
2026-08-09
Start date
2026-08-28
Completion date
Unknown
Last updated
2026-08-10

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

Conditions

Late-life depression with cognitive control impairment

Interventions

Elderly depression patients with cognitive control impairment:Escitalopram tablets (10mg-20mg/ day, centralized procurement, Shandong Jingwei Pharmaceutical Co., LTD.) or sertraline hydrochloride tabl

Sponsors

Beijing An Ding Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 60-75 years, Han Chinese, right-handed, both genders. 2. Meet the diagnostic criteria for depressive disorder according to DSM-5. 3. First episode, never received systematic antidepressant treatment, disease duration within 2 years. 4. HAMD-17 >=17 points (moderate depression or above). 5. At least one of the Trail Making Test (TMT-A and TMT-B) completion times is more than one standard deviation or more above the normal control (compared with the completion times of normal elderly controls previously recruited by our research group). 6. Mini-Mental State Examination (MMSE) >20 points for primary school education, and MMSE >24 points for others. 7. Education level of primary school or above, able to understand the scale or test content. 8. Obtain written informed consent from the subject and their family.

Exclusion criteria

Exclusion criteria: 1. Visual or auditory abnormalities. 2. Significant suicide risk (item 3 score of HAMD-17 >=3). 3. Subjects meeting DSM-5 diagnostic criteria for other mental disorders, such as schizophrenia spectrum and other psychotic disorders, bipolar disorder, anxiety disorders, obsessive-compulsive and related disorders, trauma- and stressor-related disorders, dissociative disorders, etc. 4. History of cranial disease, brain injury, epilepsy, or other neurological diseases. 5. History of severe systemic diseases involving the cardiovascular, respiratory, or immune systems. 6. History of substance abuse, active suicidal attempts, or electroconvulsive therapy. 7. Presence of metal implants such as dentures, aneurysm clips, pacemakers, or metal fixators. 8. Taking lorazepam >2 mg/day (or equivalent benzodiazepines). 9. Pregnant, breastfeeding, or planning to become pregnant.

Design outcomes

Primary

MeasureTime frame
Overall cognitive function;Depressive symptoms;Executive function;Brain connection;Model performance;

Secondary

MeasureTime frame
Adverse event;

Countries

China

Contacts

Public ContactLiu Chaomeng

Beijing An Ding Hospital, Capital Medical University

112019000189@ccmu.edu.cn+86 10 58340201

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026