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mHealth Titration and Management

Primary Purpose

Diabetes Mellitus, Type 2, Diabetic Complication

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
iSage App with connected glucometer
Magnet
Sponsored by
Amalgam Rx, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2

Eligibility Criteria

21 Years - 100 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • T2DM (WHO criteria) treated with basal insulin (glargine, detemir, degludec)
  • HgbA1c 8 or above
  • GFR >60 ml/min within the last 12 months
  • English speaking, informed consent
  • Has an Android or iOS based compatible smartphone (iOS 9.0 or above; Android 4.4 or above)
  • Currently performs at least 3 fasting fingerstick glucose measurements/week
  • Have a PCP within the KU Health System

Exclusion Criteria:

  • Diagnosis of hypoglycemic unawareness within 6 months of enrollment
  • Diagnosis of hyperglycemic hyperosmolar non-ketotic coma (HONK) or diabetic ketoacidosis (DKA) within 6 months of enrollment
  • Recent (within the last 6 months)/current use of non-topical steroids
  • Insulin requirements in excess of 1U/kg per day
  • Use of pioglitazone or another thiazolidinedione (TZD)
  • In the opinion of the provider, HgbA1c goals should adjusted above 7% due to infirmity, unstable cardiovascular disease, etc.

Sites / Locations

  • Cray Diabetes Self-Management CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

iSage

Conventional Management

Arm Description

The provider will choose a treatment algorithm embedded within the app and set the parameters to make insulin dose adjustments no less frequently than every 7 days. The app is downloaded by the patient while in the examination room, and the patient is instructed to perform daily fasting glucose fingerstick measurements and follow the app's recommendations for insulin adjustment. Data on telephone or visit contact with a healthcare provider will be collected via the EMR. Hypoglycemic events (defined as blood glucose <70 mg/dl, measured or perceived) are recorded in the iSage application as well as patient report. Providers are asked to review the patients transmitted blood sugar logs as necessary, and those reviews are recorded. Return visits are managed by the HCP and will be logged as resource utilization.

Our clinic uses a modified treat-to-target algorithm which is summarized on a 3 x 5 refrigerator magnet. In the case of glargine or detemir (Basaglar, Lantus, Levemir) adjustments of 1 unit of insulin/day are made until the fasting blood sugars (2 of 3 consecutive values) are 80-130 mg/dl. In the instance of Toujeo or Tresiba, adjustments of 2 units are made every 5 days. Volunteers will have meters downloaded (or interviewed where necessary) to obtain data on fasting blood sugar and episodes of hypoglycemia (perceived or measured <70 mg/dl). The PCP is free to request glucose logs and set return appointments as needed to manage the patient.

Outcomes

Primary Outcome Measures

Change in A1C
Mean and Median Change from Baseline

Secondary Outcome Measures

A1C in Target
Percentage of patients with an A1C < 7
Rate of Hypoglycemia
Percentage of glucose readings <70

Full Information

First Posted
April 8, 2019
Last Updated
April 8, 2019
Sponsor
Amalgam Rx, Inc.
Collaborators
Kansas City Area Life Sciences Institute, Inc., University of Kansas, LifeScan
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1. Study Identification

Unique Protocol Identification Number
NCT03908762
Brief Title
mHealth Titration and Management
Official Title
Use of a Digital Therapeutic and Connected Devices to Support Insulin Titration
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2019 (Actual)
Primary Completion Date
December 2019 (Anticipated)
Study Completion Date
March 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Amalgam Rx, Inc.
Collaborators
Kansas City Area Life Sciences Institute, Inc., University of Kansas, LifeScan

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
The principal objective of this application is to improve glycemic control of diabetic patients treated with basal insulin through use of an innovative, FDA-cleared smartphone-based insulin titration application connected to Bluetooth enabled glucose meters. iSage Rx (isageapp.com) allows providers to prescribe basal insulin treatment plans to patients and manages basal insulin doses utilizing clinically proven algorithms. In this pilot study, we hypothesize that this user-friendly application and seamless data capture will improve glycemic control (achieve HgbA1c <7%) and reduce the frequency and severity of hypoglycemia. Exploratory measures will include healthcare resource utilization and patient and provider satisfaction. The basal insulin titration algorithms used in iSage have had thousands of user-years' experience in FDA-mandated, closely supervised clinical trials, both for long-acting insulins (e.g., Lantus, Levemir) that have been available for a long time and for the newer ultra-long-acting ones (e.g., Tresiba, Toujeo). However, the effectiveness of iSage with a connected glucose meter has not been studied in a "real world" clinical environment. Broad use of such an application and connected devices will, we believe, prove to be cost-effective, favor early and appropriate prescription of insulin, reduce provider effort, shorten time to achieve glycemic goals, and simplify the transition to basal insulin therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2, Diabetic Complication

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
iSage
Arm Type
Experimental
Arm Description
The provider will choose a treatment algorithm embedded within the app and set the parameters to make insulin dose adjustments no less frequently than every 7 days. The app is downloaded by the patient while in the examination room, and the patient is instructed to perform daily fasting glucose fingerstick measurements and follow the app's recommendations for insulin adjustment. Data on telephone or visit contact with a healthcare provider will be collected via the EMR. Hypoglycemic events (defined as blood glucose <70 mg/dl, measured or perceived) are recorded in the iSage application as well as patient report. Providers are asked to review the patients transmitted blood sugar logs as necessary, and those reviews are recorded. Return visits are managed by the HCP and will be logged as resource utilization.
Arm Title
Conventional Management
Arm Type
Active Comparator
Arm Description
Our clinic uses a modified treat-to-target algorithm which is summarized on a 3 x 5 refrigerator magnet. In the case of glargine or detemir (Basaglar, Lantus, Levemir) adjustments of 1 unit of insulin/day are made until the fasting blood sugars (2 of 3 consecutive values) are 80-130 mg/dl. In the instance of Toujeo or Tresiba, adjustments of 2 units are made every 5 days. Volunteers will have meters downloaded (or interviewed where necessary) to obtain data on fasting blood sugar and episodes of hypoglycemia (perceived or measured <70 mg/dl). The PCP is free to request glucose logs and set return appointments as needed to manage the patient.
Intervention Type
Device
Intervention Name(s)
iSage App with connected glucometer
Intervention Description
Providers prescribe an insulin dosing plan to patients and provide them with a connected glucometer. The patient's plan is administered through a mobile application. In addition, patients receive education and guidance on insulin administration.
Intervention Type
Behavioral
Intervention Name(s)
Magnet
Intervention Description
Patients are given a refrigerator magnet with an insulin titration algorithm and are asked to follow the instructions on the magnet.
Primary Outcome Measure Information:
Title
Change in A1C
Description
Mean and Median Change from Baseline
Time Frame
3 Months
Secondary Outcome Measure Information:
Title
A1C in Target
Description
Percentage of patients with an A1C < 7
Time Frame
Baseline to 3 months
Title
Rate of Hypoglycemia
Description
Percentage of glucose readings <70
Time Frame
Baseline to 3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: T2DM (WHO criteria) treated with basal insulin (glargine, detemir, degludec) HgbA1c 8 or above GFR >60 ml/min within the last 12 months English speaking, informed consent Has an Android or iOS based compatible smartphone (iOS 9.0 or above; Android 4.4 or above) Currently performs at least 3 fasting fingerstick glucose measurements/week Have a PCP within the KU Health System Exclusion Criteria: Diagnosis of hypoglycemic unawareness within 6 months of enrollment Diagnosis of hyperglycemic hyperosmolar non-ketotic coma (HONK) or diabetic ketoacidosis (DKA) within 6 months of enrollment Recent (within the last 6 months)/current use of non-topical steroids Insulin requirements in excess of 1U/kg per day Use of pioglitazone or another thiazolidinedione (TZD) In the opinion of the provider, HgbA1c goals should adjusted above 7% due to infirmity, unstable cardiovascular disease, etc.
Facility Information:
Facility Name
Cray Diabetes Self-Management Center
City
Kansas City
State/Province
Kansas
ZIP/Postal Code
66160
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Teri Lavenbarg
Phone
913-588-6022
Email
tlavenbarg@kumc.edu
First Name & Middle Initial & Last Name & Degree
David Robbins
First Name & Middle Initial & Last Name & Degree
Kristin Grdinovac

12. IPD Sharing Statement

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mHealth Titration and Management

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