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Smart Glucose Meter Project

Primary Purpose

Type 1 Diabetes, Type 2 Diabetes

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Telcare Blood Glucose Meter (BGM)
Sponsored by
University of Maryland, Baltimore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 1 Diabetes focused on measuring SMBG (self monitoring of blood glucose), diabetes, mobile technology

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 years of age and older
  • Diagnosis of Diabetes Mellitus (Type 1 or Type 2)
  • Currently, non-compliant with prescribed glucose testing regimen
  • HbA1c of 7.5 or greater within the last six months

Exclusion Criteria:

  • Actively being treated for substance abuse
  • Treatment for a thought disorder within the past year
  • Non-English speaking
  • Persons who are legally blind
  • Women who are pregnant
  • Cognitively or decisionally impaired as determined by practitioner
  • Persons using an insulin pump

Sites / Locations

  • University of Maryland

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Control

Intervention

Arm Description

Provider-driven care, based in office, no special diabetes management; Patient self-monitoring of blood glucose (SMBG)

Home diabetes monitoring by patient using cellular enabled glucometer to communicate information and receive feedback. Care provider can access raw and analyzed patient data; Physician receives report summary.

Outcomes

Primary Outcome Measures

Change in HbA1c
Determine whether this intervention leads to significant improvements in patient HbA1c from baseline to 6 months

Secondary Outcome Measures

Full Information

First Posted
February 7, 2011
Last Updated
May 4, 2023
Sponsor
University of Maryland, Baltimore
Collaborators
Maryland Industrial Partnerships, Telcare, Inc
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1. Study Identification

Unique Protocol Identification Number
NCT01341587
Brief Title
Smart Glucose Meter Project
Official Title
Comparison of a Cellular-embedded Glucose Meter With Two-way Personalized Communication Between Patients and Care Managers With a Glucose Meter in Standard Practice in the Care of Diabetic Patients.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Terminated
Why Stopped
participants lost to follow-up;
Study Start Date
April 2011 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
June 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Maryland, Baltimore
Collaborators
Maryland Industrial Partnerships, Telcare, Inc

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Currently, in the U.S., 1 in 3 males and 2 in 5 females born after 2000 are expected to develop diabetes during his or her lifetime. Research has demonstrated that control of blood glucose (BG) reduces the complications of diabetes. As a result, almost half of Americans diagnosed with diabetes, are prescribed finger-stick glucose meters to monitor their BG. The value of this approach is known to be limited by a high rate of patient non-compliance with BG testing, where patients test less often than prescribed. Increased communication between patient and care manager along with feedback has been shown to increase self monitoring of blood glucose (SMBG) test compliance. However, this feedback loop is largely absent from the current, episodic model of patient / care manager interaction and not available in existing BG meters given to diabetic patients. In this study, we propose to pilot test a cellular-embedded glucose meter. This device can transmit glucose readings directly over a cellular network to a care management server and then the patient will receive feedback on the screen of the glucose meter.
Detailed Description
This research program will enroll participants in a 6-month pilot intervention study. In this study, 100 patients with diabetes (Type 1 and Type 2) who are known to be non-compliant with SMBG will be enrolled and randomized to treatment groups (one group will receive a standard glucose meter and the second group will receive the cellular-embedded device) in order to achieve the following specific study aims; Primary Aim 1: Determine if connecting diabetic patients to care managers via a cellular-enabled glucose meter with feedback will improve SMBG testing compliance. Secondary Aim 2: Determine if increased testing compliance leads to improvement in overall blood glucose control. This will be measured by a reduction of HbA1c levels. Secondary Aim 3: Determine whether this intervention leads to significant improvements in patient satisfaction with self-care and patient self-assessment of compliance.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes, Type 2 Diabetes
Keywords
SMBG (self monitoring of blood glucose), diabetes, mobile technology

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Provider-driven care, based in office, no special diabetes management; Patient self-monitoring of blood glucose (SMBG)
Arm Title
Intervention
Arm Type
Active Comparator
Arm Description
Home diabetes monitoring by patient using cellular enabled glucometer to communicate information and receive feedback. Care provider can access raw and analyzed patient data; Physician receives report summary.
Intervention Type
Device
Intervention Name(s)
Telcare Blood Glucose Meter (BGM)
Intervention Description
Cellular enabled glucometer
Primary Outcome Measure Information:
Title
Change in HbA1c
Description
Determine whether this intervention leads to significant improvements in patient HbA1c from baseline to 6 months
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years of age and older Diagnosis of Diabetes Mellitus (Type 1 or Type 2) Currently, non-compliant with prescribed glucose testing regimen HbA1c of 7.5 or greater within the last six months Exclusion Criteria: Actively being treated for substance abuse Treatment for a thought disorder within the past year Non-English speaking Persons who are legally blind Women who are pregnant Cognitively or decisionally impaired as determined by practitioner Persons using an insulin pump
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cindy Geppi
Organizational Affiliation
University of Maryland, Baltimore
Official's Role
Study Director
Facility Information:
Facility Name
University of Maryland
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States

12. IPD Sharing Statement

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Smart Glucose Meter Project

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