Utilizing Off-the-shelf Technology to Improve Diabetes Management in a Rural Population

Hypothesis: Intervening in a rural primary care population with a clinically validated
telehealth tool (Epharmix Diabetes) that algorithmically triages patients and facilitates
patient-provider communication will result in a statistically significant improvement in the
indicators of diabetes control.

Study Design

- Study Type: Experimental, non-controlled crossover study (intervention vs. standard of
care for clinic)

- Primary aim: decrease average self-tested pre-prandial blood glucose level and HgbA1C

- Secondary aim: decreased number of disease-related emergency room (ER) visits, decreased
number of self-reported blood glucose measurements outside of goal

- Duration: 3 months + 1 month enrollment period

- Safety: Protocol will be under direction of University of Missouri Institutional Review
Board (IRB). All patients will be referred to emergency department if unsafe blood
glucose levels are reported. All information is encrypted and HIPAA compliant.

- Sample Size: Clinic flow analysis estimates 61 patients eligible for study (5 providers,
assuming 30% of eligible patients who meet inclusion criteria during 4-week enrollment
period interested), with 50 patients likely to stay in study (80% retention rate).

- Power analysis: Based on pilot data and assuming an alpha error = 0.05, this study will
have have greater than 80% statistical power of detecting differences in populations
using only 20 patients with a minimum detectable effect size (decrease in HgbA1C) of
0.7%

Methodology

- The investigator will supply family practice clinics at Mercy with a one-page summary
and advertisement of the intervention. At some point during a clinical encounter with a
patient with an existing or new diagnosis of diabetes, providers will invite the patient
to participate in this Community Integration Project. Providers will maintain a list of
patients interested in the study with corresponding phone numbers and the investigator
will regularly add patients to the study.

- Over a 3-month study period, patients will interact with the telehealth system twice a
day, entering blood glucose levels when prompted. As recommended by physicians at Mercy,
the investigator will message the physicians once a week with a digest of their patients
at risk through the existing electronic medical record (EMR) inbox to more easily
integrate with existing clinic flow.

- HgbA1c will be measured prior to starting intervention and will be measured within 7
days of completing intervention.

- Providers will be notified by the system when patients are triaged to be "high risk,"
that is, out of a pre-selected range of self-reported blood glucose levels. Providers
can then be automatically connected with these patients to titrate blood glucose
control.

- At the conclusion of study, new average self-reported blood glucose responses will be
compared against those averages prior to intervention and to clinic averages for
patients with diabetes. Additionally, HgbA1C levels will be compared pre and post
-intervention.

- Results will be analyzed and conclusions will be presented to participating stakeholders
in a poster session.

Inclusion Criteria:

1. Age: 18-70 years of age

2. Gender: Any gender

3. Language: patients must use English as primary language

4. Patient must be ambulatory patients at Mercy Family Practice Clinic in Rolla, Missouri

5. Patient must have access to touch tone telephone or mobile phone with texting
capability

6. Patient must have documented type 2 diabetes mellitus with a treatment plan that
includes measuring pre-prandial blood glucose levels each morning.

7. HgbA1c between 7 and 9%

Exclusion Criteria:

- Patients that are identified by clinic staff who have demonstrated noncompliance

- Lack of access to mobile or landline telephone

- Hospitalized patients