Personalized Antidepressant Adherence Strategies For Depressed Elders
Completed · Not applicable
Conditions studied: Depression
In brief
The study is a randomized controlled trial to test the usefulness of a brief intervention to improve adherence to antidepressant medication prescribed to older adults in a primary care setting. Study will be conducted at Weill Cornell and University of Michigan.
Key facts
- Study ID
- NCT01301859
- Run by
- Weill Medical College of Cornell University
- People needed
- 231
- Starts
- 2011-01-01
- Expected to finish
- 2016-06-01
- Last updated by the study team
- 2017-01-13
Who can join
Age: 65 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age: 65 and older; Newly prescribed antidepressant medication by PCP (within past 10 days); Has not been prescribed antidepressant medication in previous 6 months.
You may not qualify if…
- High suicide risk, i.e. intent or plan to attempt suicide Presence of alcohol abuse, substance abuse, psychotic disorder or, bipolar disorder as observed on the SCID, are excluded; Dementia: MMSE below 24, clinical assessment, or medication; Inability to speak English; Aphasia interfering with communication; Terminal illness or current chemotherapy
Where it is running
- University of Michigan — Ann Arbor, Michigan, United States
- Weil Cornell Medical College — New York, New York, United States
Full record on ClinicalTrials.gov
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