My Diabetes, My Community
Study Details
Study Description
Brief Summary
Older adults with diabetes are a highly vulnerable population that suffers the highest rates of cardiovascular and microvascular complications as well as adverse drug events such as hypoglycemia. Investigators will conduct a 12-month pragmatic clinical trial evaluating the impact of scalable interventions that are designed to support personalized goal setting and self-care through remote delivery of clinical and socioeconomic risk assessment, telephonic care management, and community resource linkage. This highly personalized approach to diabetes care has to potential to improve quality of life of this high-risk population while avoiding adverse drug events.
Condition or Disease | Intervention/Treatment | Phase |
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N/A |
Detailed Description
To address the needs of older patients with diabetes, multiple organizations have called for a personalized approach to setting risk factor goals and self-care plans. The American Geriatrics Society (AGS) and the American Diabetes Association (ADA) have published recommendations urging individualized glycemic goals (hemoglobin A1C (A1C) <7.5%, <8.0%, or <8.5%) for three strata of older patients (healthy, complex, very complex). The guidelines also acknowledge the importance of addressing socioeconomic risks that are barriers to self-care management such as cost-related non-adherence and food insecurity. Despite widespread agreement by experts, the clinical impact of this highly personalized approach to diabetes care for older adults has been rarely studied in controlled trials. Interventions designed to personalize diabetes care must overcome multiple challenges to implementation including the brief clinical encounter, lack of patient engagement between encounters, and lack of systems to leverage community-based self-care resources.
Investigators propose to address these knowledge and care gaps by studying the integration of two evidence-based interventions designed to engage patients and enhance self-care:. Managing Diabetes to Gain Opportunities for a More Active Life (My Diabetes GOAL) and CommunityRx. The My Diabetes GOAL intervention is designed to engage older patients in personalized goal setting and chronic disease management.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
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No Intervention: Attention Control Subjects monthly calls similar in structure to the intervention arms, but without support. (attention placebo control) |
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Active Comparator: My Diabetes Goal My Diabetes Goal protocol |
Behavioral: My Diabetes Goal
Subjects enrolled in the MDG arm will receive surveys at baseline, 6 months and 12 months, followed by monthly diabetes care management phone calls.
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Active Comparator: My Diabetes Goal + Community Rx My Diabetes Goal protocol + Community Rx protocol |
Behavioral: My Diabetes Goal + CommunityRx
Subjects enrolled in the MDG arm + CRx will receive surveys at baseline, 6 months and 12 months, followed by monthly diabetes care management phone calls. Participants will also receive a HealtheRx (personalized resource "prescriptions") for community organizations.
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Outcome Measures
Primary Outcome Measures
- A1c [Baseline to 12 months]
Change in A1c
Secondary Outcome Measures
- Assessment of personalized diabetes care goal [Baseline to 12 months]
Investigators will compare diabetes care goals documented in the EHR against the study survey. The possible values will be yes or no goals documented in the EHR.
- Patients' ability to reach personalized goals [Baseline to 12 months]
Investigators will measure whether or not patients are reaching the goals they have documented in the survey, among those who have set up their personalized goals. The possible values will be yes or no reaching personalized goals.
- Diabetes Self-Efficacy [Baseline to 12 months]
Evaluate subject self-efficacy through the diabetes empowerment scale.
Eligibility Criteria
Criteria
Inclusion Criteria:
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History of type 2 diabetes
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Seen in clinic within past year
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A1C>7.5%
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Community dwelling
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Access to personal email address OR internet access
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Speaks and reads English
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Resides in the target geographic region (zip codes)
Exclusion Criteria:
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Unable to consent to study for themselves
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Prior participation in CRxCaregiver, CRxHunger, or My Diabetes GOAL trials
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
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1 | University of Chicago Medicine | Chicago | Illinois | United States | 60637 |
Sponsors and Collaborators
- University of Chicago
- National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Investigators
- Principal Investigator: Elbert Huang, University of Chicago
- Principal Investigator: Stacy Lindau, University of Chicago
Study Documents (Full-Text)
More Information
Publications
None provided.- IRB20-0870
- 1R01DK127961-01