A Randomized Controlled Trial Evaluating One Drop | Premium With Afrezza vs. One Drop | Premium Alone

Sponsor
Informed Data Systems, Inc. (Industry)
Overall Status
Unknown status
CT.gov ID
NCT03313960
Collaborator
Mannkind Corporation (Industry)
400
1
2
26.8
14.9

Study Details

Study Description

Brief Summary

The A-One study is a prospective, randomized controlled trial evaluating the use of the One Drop | Premium 'On Track' in combination with Afrezza treatment on the glycemic control, treatment adherence, social-cognitive barriers to adherence, and treatment satisfaction of people with Type 2 diabetes (T2D) and a hemoglobin A1c (A1c) > 7.0% already prescribed an injectable rapid-acting insulin.

Condition or Disease Intervention/Treatment Phase
  • Drug: Afrezza plus One Drop | Premium
  • Other: One Drop | Premium
Phase 4

Detailed Description

Eligible participants (N=400) with an A1c > 7.0% already prescribed a rapid-acting insulin will be randomized to one of two groups: (1) One Drop | Premium 'On Track' (i.e., use the One Drop | Mobile app with in-app diabetes education accredited by the American Diabetes Association with supplemental Afrezza content and a live Certified Diabetes Educator messaging in the app, the 'Chrome' Bluetooth-connected blood glucose meter that uploads blood glucose values in the app, and 150 test strips per month) in combination with Afrezza treatment (n=200) or (2) One Drop | Premium 'On Track' plus their current rapid-acting insulin (n=200).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
400 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A-One: A Randomized Controlled Trial Evaluating One Drop | Premium With Afrezza vs. One Drop | Premium Alone
Actual Study Start Date :
Oct 5, 2017
Actual Primary Completion Date :
Sep 30, 2018
Anticipated Study Completion Date :
Dec 30, 2019

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: One Drop | Premium with Afrezza

Drug: Afrezza plus One Drop | Premium
Participants in this group will receive insulin inhalation, prescribed by their physician, and will also receive One Drop | Premium (i.e., One Drop | Experts in-app coaching from a Certified Diabetes Educator (CDE) along with One Drop | Chrome Bluetooth-connected blood glucose meter that uploads results into the One Drop | Mobile app and 150 test strips per month for three months).
Other Names:
  • insulin inhalation
  • Other: One Drop | Premium without Afrezza

    Other: One Drop | Premium
    Participants in this group will receive One Drop | Premium (i.e., One Drop | Experts in-app CDE coaching with the One Drop | Chrome Bluetooth-connected blood glucose meter that uploads results into the One Drop | Mobile app and 150 test strips per month for three months).

    Outcome Measures

    Primary Outcome Measures

    1. Hemoglobin A1c [3 months]

      3-month between-group change in A1c assessed by a central lab

    Secondary Outcome Measures

    1. Insulin Device Satisfaction [3 months]

      Within- and between-group change in insulin device satisfaction assessed by the Insulin Device Satisfaction Survey (IDSS)

    2. Treatment Adherence [3 months]

      Within- and between-group change in treatment adherence assessed by the Adherence to Refills and Medications Scale for Diabetes (ARMS-D) and the Summary of Diabetes Self-care Activities Medications Subscale administered for each oral diabetes medication (SDSCA-MS) and insulin in the regimen (SDSCA-IS).

    3. Self-care [3 months]

      Within- and between-group change in self-care assessed by the SDSCA's other subscales

    4. Health-related Productivity [3 months]

      Within- and between-group change in health-related productivity assessed by the Work Productivity and Activity Impairment measure (WPAI).

    5. Health-related Quality of Life [3 months]

      Within- and between-group change in health-related quality of life assessed by the Centers for Disease Control Health-related Quality of Life-14 (CDC HRQOL-14) and life satisfaction assessed by the Cantril Self-Anchoring Ladder of Life Satisfaction.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • 18-75 years of age

    • Self-reported diagnosis of T2D

    • Diagnosed with diabetes for at least 12 months

    • Prescribed a prandial rapid-acting insulin

    • Willing to take Afrezza rapid-acting insulin for 3 months instead of current rapid-acting insulin

    • Willing to get a physician's prescription for Afrezza

    • Self-reported A1c > 7.0% (later confirmed with a mail-in A1c laboratory test)

    • Owns and uses an iPhone or Android phone with an operating system compatible with the One Drop | Mobile app

    • Has successfully downloaded and used a smart phone application previously

    Exclusion Criteria:
    • Currently pregnant or planning to become pregnant during the trial period

    • Cannot read or write in English

    • Currently in a diabetes education or coaching program

    • Had previously used One Drop | Premium or One Drop |

    • Experts coaching

    • Had previously used or is currently using Afrezza

    • Currently smokes (cigaretts, e-cigs, pipes, cigars, marijuana) or has smoked anytime in the past 6 months

    • Has chronic lung disease, e.g., COPD and asthma

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 One Drop New York New York United States 10002

    Sponsors and Collaborators

    • Informed Data Systems, Inc.
    • Mannkind Corporation

    Investigators

    • Principal Investigator: Chandra Osborn, PhD, MPH, Informed Data Systems, Inc. | One Drop

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Chandra Osborn, PhD, MPH, Vice President, Health & Behavioral Informatics, Informed Data Systems, Inc.
    ClinicalTrials.gov Identifier:
    NCT03313960
    Other Study ID Numbers:
    • A-One
    First Posted:
    Oct 19, 2017
    Last Update Posted:
    Feb 26, 2019
    Last Verified:
    Feb 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Chandra Osborn, PhD, MPH, Vice President, Health & Behavioral Informatics, Informed Data Systems, Inc.
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 26, 2019