Integrating Depression Services Into DM Management
Completed · Not applicable
Conditions studied: Type 2 Diabetes Mellitus, Depression
In brief
The goal of this proposal is to integrate depression services into improving adherence for oral hypoglycemic agents so that a single program can assist patients. The investigators hypothesized that patients in the intervention would demonstrate improved adherence to patients' oral hypoglycemic agents and antidepressants as well as improved clinical outcomes.
Key facts
- Study ID
- NCT01098253
- Run by
- University of Pennsylvania
- People needed
- 182
- Starts
- 2009-01-01
- Expected to finish
- 2011-04-01
- Last updated by the study team
- 2012-03-09
Who can join
Age: 30 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 30 years and older
- a current diagnosis of Type 2 DM
- current prescription for an oral hypoglycemic agent
- current prescription for an antidepressant
- able to communicate in English
- willing to give informed consent.
You may not qualify if…
- inability to give informed consent
- significant cognitive impairment at baseline (Mini-Mental State Examination (MMSE) <21)
- residence in a care facility that provides medications
- unwillingness or inability to use the Medication Event Monitoring System
Where it is running
- University of Pennsylvania — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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