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N/A Completed N=7,052 Randomized Prevention

Blood Glucose Monitoring in Electronic Health Records

Source: ClinicalTrials.gov NCT03542487 ↗
Enrolled (actual)
7,052
Serious AEs
—
Results posted
Sep 2024
Primary outcomePrimary: Count of Participants Entering Flowsheet Data During Measurement Period, Extensive Margin — 4; 27; 44; 43 Participants

Summary

This multi-site randomized tral aims to test methods of increasing adoption and integration of blood glucose monitoring into electronic medical records, and to measure the impact of wide-scale adoption on health status of patients with diabetes. To investigate determinants of adoption, the research will combine and test doctor and patient focused approaches to encouraging patient use of blood glucose flow sheets through the online patient portal, MyChart. Adoption will be measured on both the extensive and intensive margin: the number of patients who enter data into the flowsheets at all during the study period, and the mean number of entries per patient during the study period. Conditional on statistically significant increases in adoption, the study will examine corresponding intent-to-treat effects on patient A1c, and consider other indicators of possible mechanisms through which A1c improves or does not improve.

Outcome Measures

OutcomeResultp-value
PRIMARY
Count of Participants Entering Flowsheet Data During Measurement Period, Extensive Margin
4; 15; 17; 20; 30 —
PRIMARY
Participant A1c Test Results (as Percent A1c) at 26 Weeks
7.179; 7.327; 7.110; 7.227; 7.227 —
SECONDARY
Count of Participants Entering Flowsheet Data During Measurement Period, Extensive Margin
4; 15; 17; 20; 30 —
SECONDARY
Number of Days Participant Used Flowsheet, Intensive
0.011; 0.501; 0.350; 0.663; 0.691; 0.009 —
SECONDARY
Count of Participants With an Open Physician Order for Electronic Glucose Flowsheet
5; 466; 589; 554; 573; 6 —
SECONDARY
Number of Days Since Last HbA1c Test
196.369; 196.828; 205.607; 192.341; 210.748; 196.434 —
SECONDARY
Participant A1c Test Results (as Percent A1c) at 14 Weeks
7.196; 7.276; 7.123; 7.183; 7.197 —
SECONDARY
Count of Participants With Improvement of HbA1c Test Results
666; 155; 158; 160; 147; 961 —
SECONDARY
Count of Participants With Percent A1c Below Benchmark of 7
1846; 388; 453; 442; 458; 1799 —
SECONDARY
Total Secure Messages Sent by Participant
1.385; 1.407; 1.528; 1.434; 1.571; 1.128 —
SECONDARY
Total Secure Messages Sent by Patient to Primary Care Provider
— —
SECONDARY
Total Secure Messages Sent by PCP to Patient
— —
SECONDARY
Total Number of Participant Phone Appointments
0.792; 0.827; 0.789; 0.849; 0.765; 1.442 —
SECONDARY
Total Number of Participant In-person Appointments
1.275; 1.314; 1.251; 1.109; 1.191; 2.326 —
SECONDARY
Count of Participants With Changes to Active Medication List
742; 135; 133; 141; 140; 1132 —
SECONDARY
Prescription Orders
5.111; 5.912; 4.488; 4.733; 4.259; 9.296 —
SECONDARY
Flowsheet Entry Values (Descriptive)
— —

Eligibility Criteria

Inclusion Criteria

  • Adult patients of Inova physicians at primary care sites other than Ashburn II Primary Care, Lake Ridge Primary Care and Springfield Primary Care
  • Current diabetes mellitus diagnosis
  • Active MyChart account at time of treatment administration

Exclusion Criteria

  • Patients who participating physicians identify as pregnant
  • Patients who participating physicians identify as having contraindications for tracking of blood glucose
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03542487). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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