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Assessing Anterior Cingulate Brain Activity in People With Late-Life Depression

Anterior Cingulate Activation in Geriatric Depression

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00926653
Enrollment
76
Registered
2009-06-23
Start date
2005-07-31
Completion date
2010-05-31
Last updated
2015-08-11

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

Conditions

Depression

Keywords

Geriatric Depression

Brief summary

This study will examine differences in activity of the anterior cingulate cortex, a brain area involved in emotion and cognitive regulation, between older adults with and without depression.

Detailed description

Older adults with depression often also suffer from executive dysfunction-problems with planning, impulse control, and reasoning. Executive dysfunction in older adults predicts poor or delayed response to antidepressant treatment and has been associated with early relapse and recurrence of late-life major depression. Functional magnetic resonance imaging (fMRI) is a scan that can measure the activity of someone's brain while that person performs tasks. So far, no fMRI studies investigating cerebral activation patterns in late-life depression have been published. In this study, people will undergo fMRI while they are performing an executive function task. Older adults with late-life depression and older adults without depression will be tested and compared in order to identify the areas and patterns of brain activity underlying executive dysfunction in late-life depression. Participation in this study will consist of one study visit, during which participants will undergo an fMRI scan that will last 60 to 90 minutes. While being scanned, participants will perform cognitive tasks that involve pressing buttons in response to words viewed on a screen.

Interventions

DRUGEscitalopram

10 to 20 mg daily as part of another study in which participants are enrolled

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
60 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

for Depressed Participants: * Diagnosis of major depression by DSM-IV criteria * Mini-Mental State Examination (MMSE) score greater than 24 * Severity score of 17 or higher on the 21-item Hamilton Depression Rating Scale score (HDRS) during the index episode * Residence less than a 45-minute drive from New York Hospital-Westchester Division

Exclusion criteria

for Depressed Participants: * Presence of psychotic depression, as defined by Research Diagnostic Criteria and DSM-IV * History of psychiatric disorders other than unipolar major depression (people with bipolar disorder and dysthymia will be excluded) * Presence of dementing disorders * Acute or severe medical illness, such as the following: delirium; metastatic cancer; decompensated cardiac, liver, or kidney failure; major surgery; or cerebrovascular accident or myocardial infarction 3 months prior to study entry * Receiving drugs known to cause depression, including reserpine, alpha-methyl-dopa, and steroids * Requires concomitant treatment with other psychotropics, including antipsychotic medications, lithium salts, stimulants, valproic acid, carbamazepine, or gabapentin * Severe aphasia interfering with communication * Contraindications to magnetic resonance (MR) scanning, such as implanted metal, claustrophobia, or weight greater than or equal to 300 lbs Inclusion Criteria for Age-Matched Non-Psychiatric Comparison Sample: * MMSE score greater than 24

Design outcomes

Primary

MeasureTime frame
Cerebral activation, as measured using functional magnetic resonance imaging (fMRI)Average of a 2 hour MRI session

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026