Last updated: July 28, 2021
Sponsor: University of California, San Francisco
Overall Status: Completed
Phase
N/A
Condition
Depression (Major/severe)
Depression
Affective Disorders
Treatment
N/AClinical Study ID
NCT02440815
ROI MH101472
Ages > 65 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Current DSM-IV diagnosis of MDD, unipolar type, without psychotic features and 6 weeksminimum duration of current depressive episode.
- Moderate severity of depression using the Hamilton Depression Rating Scale (HDRS > 20).
- English speaking, male or female
- 65 years of age or older
- Good general health
- Able to give informed consent
Exclusion
Exclusion Criteria:
- Antidepressant use or psychotherapy within the past 6 weeks or electroconvulsivetherapy within the past 6 months.
- Recent history (<6 months) of substance or alcohol abuse or dependence (DSM-IVcriteria).
- Use of cognitive enhancing medications.
- Current diagnosis of Post-Traumatic Stress Disorder or other Axis 1 psychiatricdisorder.
- Neurological diseases (e.g., Parkinson's disease, epilepsy, cortical stroke,Alzheimer's disease, traumatic brain injury) or dementia.
- History of surgical procedures affecting study outcomes.
- Contraindications for MR exam, i.e., no claustrophobia, no paramagnetic metalimplants, able to fit in the MRI machine comfortably (BMI ≤ 38).
- Acute or uncontrolled medical illness or medication use impacting cognitive function.
Study Design
Total Participants: 108
Study Start date:
November 01, 2015
Estimated Completion Date:
July 28, 2021
Study Description
Connect with a study center
University of California, San Francisco, Langley Porter Psychiatric Institute
San Francisco, California 94143
United StatesSite Not Available

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