Actively Recruiting
Glucose Management Clinical Decision Support to Improve Outcomes in Academic and Community Hospitals
Led by Milton S. Hershey Medical Center · Updated on 2026-05-14
15732
Participants Needed
2
Research Sites
52 weeks
Total Duration
On this page
Sponsors
M
Milton S. Hershey Medical Center
Lead Sponsor
N
National Institutes of Health (NIH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the impact of an electronic medical record clinical decision support (CDS) tool on controlling abnormal blood sugar levels, known as dysglycemia, in hospitalized patients with diabetes or stress-related hyperglycemia. The study aims to examine how this tool affects clinical outcomes, hospital costs, and healthcare providers' knowledge and practice performance in both academic and community hospital settings. This research involves non-intensive care patients and explores the tool’s influence on improving hospital care delivery and reducing complications related to high glucose. The study uses an innovative alert-CDS tool integrated into the electronic medical record system. This tool automatically identifies dysglycemia and inadequate insulin use, then sends alerts with treatment recommendations to healthcare providers during active phases of the study. The trial alternates between six active 3-month periods when alerts are sent and six inactive 3-month periods without alerts, covering a total of 36 months. During inactive periods, data on care gaps are collected but alerts are not shown. This setup allows comparison between standard care and care supported by the alert-CDS tool. Participants include adult patients hospitalized or receiving ambulatory care at several hospitals within the health system. The study tracks multiple outcomes such as hospital length of stay, glycemic control measures, rates of complications, mortality, hospital resource use, and economic impacts. Provider perspectives and decision-making related to dysglycemia management are also assessed through surveys. The total observation period spans up to three months per hospital admission, with some measures extending up to a year after discharge.
CONDITIONS
Brief Title
Diabetes Clinical Decision Support
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Hospitalized adult (over 18 years) patients at Penn State Health and affiliated hospitals
- Ambulatory adult (over 18 years) patients at Penn State Health and affiliated hospitals
- Experience of an alert or disease management message related to blood sugar control
You will not qualify if you...
- Children under 18 years of age
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or via medical record review)
Duration - Up to 36 months
Participants are hospitalized patients whose clinical care is observed during alternating 3-month periods when an electronic clinical decision support tool is active or inactive in the medical record.
Continuous monitoring during hospital stay
Duration - Up to 12 months post discharge
Participants are observed for outcomes such as hospital readmission, glycohemoglobin levels, and mortality up to 12 months after hospital discharge.
Follow-up assessments after discharge as needed
Trial Site Locations
Total: 2 locations
1
Penn State Hershey Medical Center
Hershey, Pennsylvania, United States, 17033
Actively Recruiting
2
Penn State Health St. Joseph Medical Center
Reading, Pennsylvania, United States, 19605
Actively Recruiting
Research Team
A
Ariana Pichardo-Lowden, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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