My Diabetes, My Community

Sponsor
University of Chicago (Other)
Overall Status
Recruiting
CT.gov ID
NCT04970810
Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (NIH)
612
1
3
35.1
17.5

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
  • Behavioral: My Diabetes Goal
  • Behavioral: My Diabetes Goal + CommunityRx
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

Study Type:
Interventional
Anticipated Enrollment :
612 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Masking Description:
This will be a single-blind study, and subjects will blinded to the different group assignment.
Primary Purpose:
Supportive Care
Official Title:
My Diabetes, My Community
Actual Study Start Date :
Jul 29, 2021
Anticipated Primary Completion Date :
May 31, 2024
Anticipated Study Completion Date :
Jun 30, 2024

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Attention Control

Subjects monthly calls similar in structure to the intervention arms, but without support. (attention placebo control)

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.

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.

Outcome Measures

Primary Outcome Measures

  1. A1c [Baseline to 12 months]

    Change in A1c

Secondary Outcome Measures

  1. 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.

  2. 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.

  3. Diabetes Self-Efficacy [Baseline to 12 months]

    Evaluate subject self-efficacy through the diabetes empowerment scale.

Eligibility Criteria

Criteria

Ages Eligible for Study:
60 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. History of type 2 diabetes

  2. Seen in clinic within past year

  3. A1C>7.5%

  4. Community dwelling

  5. Access to personal email address OR internet access

  6. Speaks and reads English

  7. Resides in the target geographic region (zip codes)

Exclusion Criteria:
  1. Unable to consent to study for themselves

  2. Prior participation in CRxCaregiver, CRxHunger, or My Diabetes GOAL trials

Contacts and Locations

Locations

Site City State Country Postal Code
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.
Responsible Party:
University of Chicago
ClinicalTrials.gov Identifier:
NCT04970810
Other Study ID Numbers:
  • IRB20-0870
  • 1R01DK127961-01
First Posted:
Jul 21, 2021
Last Update Posted:
Aug 30, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 30, 2021