1. |
Studying clinical subgroups (phenotypes) |
2. |
Increasing patient-guided treatment/shared decision-making |
3. |
Improving/collecting information on care management approaches, coordination of care |
4. |
Collecting information from patients via Interactive Voice Response (IVR) |
5. |
Understanding patient and provider factors that play a role in intensification of diabetes treatment regimens |
6. |
Developing pragmatic trials to improve diabetes care for the elderly and Type 1 DM |
7. |
Targeting care to “high risk” individuals based on impairments in physical or mental health status (those in fair or poor health) |
8. |
“Un-complicating” diabetes care through simplifying/coordinating medication regimens |
9. |
Providing diabetes education and support in real-time through peers and/or professionals |
10. |
Integrating clinical decision support into care and existing work flows |
11. |
Developing valid, reliable data systems on diabetes education referral and follow-up |
12. |
Assessing non-adherence as a potential ‘alert’/marker of diabetes distress |