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Phase 4 N=106 Treatment

Aging Brain Changes, Executive Dysfunction and Depression

Depression

Enrolled (actual)
106
Serious AEs
6.7%
Results posted
May 2017
Primary outcome: Primary: Hamilton Depression Rating Scale. — 8.09 units on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Escitalopram (Drug)
Age
Adult, Older Adult · 60+ yrs
Sex
All
Sponsor
Weill Medical College of Cornell University
Primary completion
May 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Hamilton Depression Rating Scale.
8.09
PRIMARY
WHODAS-II Disability Scale
31.43
PRIMARY
Stroop Color-Word Test
33.63

Summary

The purpose of this study is to look at the relationship between age related structural brain changes and changes in depressive symptoms,disability and several aspects of cognitive functioning following treatment with escitalopram.

Eligibility Criteria

Inclusion Criteria

  • Age: Two strata: 60-74 years (n=60) subjects and 75-84 years (n=60).
  • Diagnosis: Major depression, unipolar (by DSM-IV criteria); or, for control subjects, no diagnosis of major depression, no history of depression or other psychiatric conditions.
  • Severity of depression: A 24-Item HDRS above 19; Level of Executive Dysfunction: Two strata within each age stratum: Stroop Color-Word scores below and above 24 (1 SD below the median of our normal elderly sample).

Exclusion Criteria

  • Psychotic depression by DSM-IV, i.e., presence of delusions with a score higher than 2 (questionable delusion) rated by the Scale for Assessment of Positive Symptoms (SAPS; 51).
  • High suicide risk, i.e. intent or plan to attempt suicide in near future.
  • Presence of any Axis I psychiatric disorder or substance abuse other than unipolar major depression.
  • Axis II diagnosis of antisocial personality (by SCID-P and DSM-IV).
  • History of psychiatric disorders other than unipolar major depression or generalized anxiety disorder (bipolar disorder, hypomania, are exclusion criteria).
  • Cognition: MMSE scores below 24 or diagnosis of dementia by DSM-IV.
  • Acute or severe medical illness, i.e., delirium, metastatic cancer, decompensated cardiac, liver or kidney failure, major surgery, stroke or myocardial infarction during the three months prior to entry; or drugs known to cause depression, e.g., reserpine, alpha-methyl-dopa, steroids.
  • Failure to respond to an adequate trial of escitalopram (10 mg/day or more for 6 weeks or longer) during the current or previous depressive episodes.
  • Current involvement in psychotherapy.
  • History of hypersensitivity to escitalopram or need to receive drugs that may interact with escitalopram.
  • Inability to perform any of the ADLs (MAI: ADL subscale) even with assistance, e.g. walking with a cane is not an exclusion criterion.
  • Inability to speak English.
  • Aphasia.
  • Residence outside a 45-minute drive from Cornell's clinical facilities.
  • Patients taking MAOI's and Fluoxetine will be excluded.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00918684). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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