Diabetes Mellitus, Type 2 Clinical Trial
— IDEAOfficial title:
Improving Diabetes Equity and Advancing Care Study
| NCT number | NCT06040463 |
| Other study ID # | 23-11 |
| Secondary ID | |
| Status | Recruiting |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | October 23, 2023 |
| Est. completion date | March 31, 2025 |
The goal of this randomized trial is to determine the optimal combination and sequence of three enhancements for a team-based care model for patients living with diabetes in Chicago. The study aim is to determine optimization of intervention components. Participants will be randomly assigned to diabetes self-management training or remote glucose monitoring. After 6 months, participants will be rerandomized to a subsequent study arm (including a CHW support program) depending on a tailoring variable of change in A1c. Researchers will compare the final 6 study arms to see which combination and sequence of enhancements produces the most improvement in A1c.
| Status | Recruiting |
| Enrollment | 270 |
| Est. completion date | March 31, 2025 |
| Est. primary completion date | March 31, 2025 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria: - A diagnosis of type 1 or type 2 diabetes - 18+ years of age - Able to provide consent - Identify as African American/Black or Latinx - most recent HbA1c > 7%, - Have a smartphone compatible with the Glooko application - Have completed at least one Center appointment (i.e. current patient) - Completed at least 3 months of their assigned study condition Exclusion Criteria: - Already an active user of RGM - Actively working with a CHW - Diagnosis of gestational diabetes (without type 1 or type 2) - Has a Power of Attorney - Be suffering from Stage-V renal disease or undergoing dialysis. - Be suffering from a severe form of cardiovascular disease (NYHA Class III and IV) |
| Country | Name | City | State |
|---|---|---|---|
| United States | Mount Sinai Hospital | Chicago | Illinois |
| Lead Sponsor | Collaborator |
|---|---|
| Sinai Health System |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in A1c | Change in A1c from baseline to the 12-month study end point measured at the patient level. Measure will be collected every 6 months, at a minimum. The 6-month A1c will be used to determine their study condition at the rerandomization poiont. | Baseline (time = 0); 6 months (time = 1); 12 months (time = 2) | |
| Secondary | Active Usage of RGM | Active usage will be defined as at least one upload of data within a 30-day period and at least 16 blood glucose entries within a 30-day period. | Data will be exported from the Glooko application monthly for the full 18 months of the trial period. | |
| Secondary | DSMT Attendance | We will collect # and proportion of attended DSMT classes by participant. | Attendance data will be collected throughout the entire study period (18 months) | |
| Secondary | CHW Support Adherence | Adherence to CHW engagement will include completing the initial education session with a CHW, competing a SDoH screener and at least three phone or in-person touchpoints over the 6-month intervention period. | After rerandomization period (starting at 6 months post enrollment) |
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