Clinical trial Recruiting at 2 sites Observational Ages 18 to 65

Improving diabetes care using data from sensors and the environment

Official title: Leveraging the Exposome and Patient Sensor Data to Enhance Personalized Diabetes Care Across Diverse Communities

Run by University of Illinois Chicago · NCT06989008 · Data updated 2026-11-12

This study is testing if using data from health records, wearable devices, and environmental sensors can help improve diabetes care for people with type 2 diabetes living in vulnerable neighborhoods.

Quick facts

Study typeObservational
Ages18 Years to 65 Years
SexAll
Enrollment20 (estimated)
SponsorUniversity of Illinois Chicago
Academic / other
Locations2 sites (Chicago, Illinois and 1 other locations)
StatusRecruiting
StartedMarch 25, 2025
Main results expectedJanuary 1, 2026
Study endsJanuary 31, 2026
Registry record updatedMay 25, 2025
Trial IDNCT06989008 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals aged 18-65 with a diagnosis of type 2 diabetes residing in specific high social vulnerability zip codes.

Probably not a fit

Patients who do not speak or understand English or those unable to follow the research protocol may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to enhance diabetes management for individuals with type 2 diabetes by integrating data from electronic health records, wearable devices, and environmental sensors. Participants will be monitored using continuous glucose monitoring (CGM) devices and physical activity trackers to gather comprehensive health data over a specified period. The study focuses on individuals living in vulnerable neighborhoods, ensuring that the findings are relevant to those who may benefit the most from personalized care. Data collection will involve both in-clinic visits and remote monitoring, allowing for a thorough analysis of how various factors influence diabetes management.

Why it matters

Potential benefit: If successful, this approach could lead to more personalized and effective diabetes care strategies for patients.

How similar studies have gone: Other studies have shown promise in using similar data integration approaches for chronic disease management, suggesting potential for success in this novel application.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria

* People with diabetes in the 18-65 years of age range
* Diagnosed with type 2 diabetes
* Resides in the specified high social vulnerability zip codes - 60619, 60620, 60621, 60636, 60644, 60624, 60609, 60612, 60617, 60623, 60628, 60629, 60639, 60645, 60649, 60651, 60652, 60653
* Speak and understand the English language
* Willing to wear various devices (CGM and sports wristband)
* Own a smartphone Exclusion Criteria
* Subjects will be excluded from the study for the following reasons:
* Any concern of not understanding informed consent
* Unable to understand or unwilling to follow research protocol

Where it's running

  • University of Illinois - Chicago
    Chicago, Illinois, United States
    Recruiting
  • University of Illinois College of Nursing
    Chicago, Illinois, United States
    Recruiting

Study contacts

  • Principal investigator: Andy Boyd, MD — University of Illinois Chicago
  • Study coordinator: Laurie Quinn, PhD
  • Email: lquinn1@uic.edu
  • Phone: 312 771 6497

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.