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Evidence for Health Improvement in People With Diabetes Using One Touch & Partner Solutions (ECLIPSE)

Primary Purpose

Diabetes Mellitus, Type 2

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cecelia Health plus OneTouch Verio Reflect® BGM and OneTouch Reveal® mobile app
Fitbit plus OneTouch Verio Reflect® BGM and OneTouch Reveal® mobile app
Noom plus OneTouch Verio Reflect® BGM and OneTouch Reveal® mobile app
Welldoc plus OneTouch Verio Reflect® BGM and Welldoc app
Sponsored by
LifeScan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

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

Eligibility Criteria

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

Inclusion Criteria:

  • Self reports a diagnosis of type 2 diabetes
  • HbA1c ≥7.5% but ≤12% at screening
  • Currently instructed by a health care provider (HCP) to use a blood glucose meter to test blood sugar
  • Has a compatible smartphone and willing to redownload apps if they change phones during the study
  • Has a stable and consistent home and/or office internet connection
  • Currently on at least 1 oral (by mouth) or injected anti-diabetic medication (for lowering your blood glucose) with or without insulin therapy (insulin injections or an insulin pump) at screening

Exclusion Criteria:

  • Currently pregnant or planning to be pregnant in the next 12 months
  • Body Mass Index < 27
  • Currently using a CGM (Continuous glucose monitor) or have used a personal CGM in the past 3 months
  • Currently using a OneTouch Verio Reflect meter
  • For FitBit arm only: Currently uses related fitness applications (e.g., MyFitnessPal, JEFIT, Fitness Coach, Yoga-Go, etc.) or wearable device (e.g., Fitbit, Apple Watch, Garmin, Withings, etc.) in the past 6 months

Sites / Locations

  • Evidation Health

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Cecelia Health

Fitbit

Noom

Welldoc

Arm Description

Access to live Cecelia health coach on the telephone for 1 year plus access to Cecelia health coach by text messaging (via the OneTouch Reveal mobile diabetes app). Subjects will be provided with the OneTouch Verio Reflect glucose meter and the OneTouch Reveal (OTR) diabetes app.

Fitbit Inspire 2 wearable plus 1 year subscription to premium Fitbit application. Subjects will also be provided with the OneTouch Verio Reflect glucose meter and the OneTouch Reveal (OTR) mobile diabetes app.

Noom behavioural weight loss program subscription for 1 year. Subjects will also be provided with the OneTouch Verio Reflect glucose meter and the OneTouch Reveal (OTR) mobile diabetes app.

Multi-condition support program from Welldoc subscription for 1 year. Subjects will also be provided with the OneTouch Verio Reflect glucose meter.

Outcomes

Primary Outcome Measures

Changes in A1c from screening to 3 and 6 months in each of the OneTouch Solutions programs

Secondary Outcome Measures

Change in mean blood glucose derived from blood glucose testing throughout the study in each of the OneTouch Solutions programs
Change from baseline in diabetes distress as assessed by the diabetes distress scale (DDS) after 3 and 6 months
Change from baseline in well-being as assessed by the WHO-5 survey after 3 and 6 months
Change from baseline in patient activation measures as assessed by PAM-13 survey after 3 and 6 months
Change from baseline in medication adherence as assessed by a medication adherence survey after 3 and 6 months

Full Information

First Posted
April 18, 2022
Last Updated
July 19, 2022
Sponsor
LifeScan
Collaborators
Evidation Health
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1. Study Identification

Unique Protocol Identification Number
NCT05354297
Brief Title
Evidence for Health Improvement in People With Diabetes Using One Touch & Partner Solutions
Acronym
ECLIPSE
Official Title
Evidence for Health Improvement in People With Diabetes Using One Touch & Partner Solutions (ECLIPSE)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
July 26, 2022 (Anticipated)
Primary Completion Date
April 1, 2023 (Anticipated)
Study Completion Date
September 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
LifeScan
Collaborators
Evidation Health

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
Data Monitoring Committee
No

5. Study Description

Brief Summary
ECLIPSE will evaluate the clinical and economic value of OneTouch Solutions in a real world study design. OneTouch Solutions describes a selection of devices and health and wellness solutions that people with diabetes (PWDs) can access online via OneTouch Solutions (Cecelia Health, Fitbit, Noom or Welldoc, each in combination with OneTouch Verio Reflect® blood glucose meter and the OneTouch Reveal® mobile app (or Welldoc app for the Welldoc arm)). ECLIPSE is a large parallel arm digital health study combining advanced blood glucose monitoring solutions with a choice of four different health and wellness applications or services. There are four unique study arms that will run in parallel over one year. The primary (A1c) endpoint for each study arm will be after 6 months and subjects will continue to use the interventions for a full year to generate data on sustained engagement with these products and services, and to collect healthcare utilization and health insurance claims information. Each study arm will differ to some degree in terms of patient baseline demographics (since subjects self-select their own app/intervention) and the experience per arm will be unique, and therefore each study arm will be analysed separately in terms of endpoints and outcomes.
Detailed Description
ECLIPSE (Evidence for health improvement in people with diabetes using One Touch & Partner Solutions) is a large parallel arm digital health study that will allow people with diabetes (PWDs) the freedom to choose the solution that is right for them, rather than forcibly randomize subjects to a specific study intervention. The intention of this real world study design is to mimic the choice PWDs will have when selecting a diabetes & digital health solution from the OneTouch Solutions website. A target of 800 people with type 2 diabetes (PwT2Ds) will be recruited and offered one of four interventions with the aim of following 200 PWDs per study arm. Subjects in all four study arms will use a bluetooth connected OneTouch Verio Reflect blood glucose meter (BGM) which features a dynamic color range indicator (DCRI) and blood sugar mentor (BSM) insights. Subjects in three of the four study arms will also sync their Reflect BGM to the OneTouch Reveal (OTR) mobile diabetes app to enable further insights (PWDs in the Welldoc study arm will not use the OTR app). The 4 unique study arms will also offer PWDs one of the following Partner offerings; Cecelia Health, which offers guidance from certified Diabetes Care and Education Specialists Fitbit, which offers activity and wellbeing insight from use of the Fitbit Inspire 2 tracker, and Fitbit Premium subscription Noom, a psychology-based weight and wellness program Welldoc, which offers personalized health coaching on multiple conditions, namely prediabetes, diabetes, hypertension and heart failure ECLIPSE will gather glycemic measures, medication adherence, a variety of patient reported outcomes and partner app usage and app engagement analytics over one year. Health economic data (HECON) from PWDs from the year of participation in ECLIPSE will be analysed from a purchased dataset and a comparison will be made to HECON data from the same PWDs for the year prior to taking part in the study. In addition, a matched control group of PwT2D from the same purchased dataset will be compared to the data from all four study arms.

6. Conditions and Keywords

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

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Cecelia Health
Arm Type
Experimental
Arm Description
Access to live Cecelia health coach on the telephone for 1 year plus access to Cecelia health coach by text messaging (via the OneTouch Reveal mobile diabetes app). Subjects will be provided with the OneTouch Verio Reflect glucose meter and the OneTouch Reveal (OTR) diabetes app.
Arm Title
Fitbit
Arm Type
Experimental
Arm Description
Fitbit Inspire 2 wearable plus 1 year subscription to premium Fitbit application. Subjects will also be provided with the OneTouch Verio Reflect glucose meter and the OneTouch Reveal (OTR) mobile diabetes app.
Arm Title
Noom
Arm Type
Experimental
Arm Description
Noom behavioural weight loss program subscription for 1 year. Subjects will also be provided with the OneTouch Verio Reflect glucose meter and the OneTouch Reveal (OTR) mobile diabetes app.
Arm Title
Welldoc
Arm Type
Experimental
Arm Description
Multi-condition support program from Welldoc subscription for 1 year. Subjects will also be provided with the OneTouch Verio Reflect glucose meter.
Intervention Type
Device
Intervention Name(s)
Cecelia Health plus OneTouch Verio Reflect® BGM and OneTouch Reveal® mobile app
Intervention Description
Expert guidance via coaching
Intervention Type
Device
Intervention Name(s)
Fitbit plus OneTouch Verio Reflect® BGM and OneTouch Reveal® mobile app
Intervention Description
Fitness and wellness guidance
Intervention Type
Device
Intervention Name(s)
Noom plus OneTouch Verio Reflect® BGM and OneTouch Reveal® mobile app
Intervention Description
Behavioral weight loss program
Intervention Type
Device
Intervention Name(s)
Welldoc plus OneTouch Verio Reflect® BGM and Welldoc app
Intervention Description
Multi condition support
Primary Outcome Measure Information:
Title
Changes in A1c from screening to 3 and 6 months in each of the OneTouch Solutions programs
Time Frame
3 and 6 months
Secondary Outcome Measure Information:
Title
Change in mean blood glucose derived from blood glucose testing throughout the study in each of the OneTouch Solutions programs
Time Frame
3 and 6 months
Title
Change from baseline in diabetes distress as assessed by the diabetes distress scale (DDS) after 3 and 6 months
Time Frame
3 and 6 months
Title
Change from baseline in well-being as assessed by the WHO-5 survey after 3 and 6 months
Time Frame
3 and 6 months
Title
Change from baseline in patient activation measures as assessed by PAM-13 survey after 3 and 6 months
Time Frame
3 and 6 months
Title
Change from baseline in medication adherence as assessed by a medication adherence survey after 3 and 6 months
Time Frame
3 and 6 months
Other Pre-specified Outcome Measures:
Title
Changes over time in the number of app sessions performed within each of the OneTouch Solutions programs
Time Frame
Over 1 year
Title
Change from baseline in A1c as a function of the number of app sessions performed within each of the OneTouch Solutions programs
Time Frame
Over 1 year
Title
Quantify the number of medical insurance claims made by subjects within each of the OneTouch Solutions programs using data harvested from a large medical insurance dataset
Time Frame
Over 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Self reports a diagnosis of type 2 diabetes HbA1c ≥7.5% but ≤12% at screening Currently instructed by a health care provider (HCP) to use a blood glucose meter to test blood sugar Has a compatible smartphone and willing to redownload apps if they change phones during the study Has a stable and consistent home and/or office internet connection Currently on at least 1 oral (by mouth) or injected anti-diabetic medication (for lowering your blood glucose) with or without insulin therapy (insulin injections or an insulin pump) at screening Exclusion Criteria: Currently pregnant or planning to be pregnant in the next 12 months Body Mass Index < 27 Currently using a CGM (Continuous glucose monitor) or have used a personal CGM in the past 3 months Currently using a OneTouch Verio Reflect meter For FitBit arm only: Currently uses related fitness applications (e.g., MyFitnessPal, JEFIT, Fitness Coach, Yoga-Go, etc.) or wearable device (e.g., Fitbit, Apple Watch, Garmin, Withings, etc.) in the past 6 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mike Grady, PhD
Phone
07775704444
Email
mgrady@lifescan.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wei-Nchih Lee, PhD
Organizational Affiliation
Evidation Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Evidation Health
City
San Mateo
State/Province
California
ZIP/Postal Code
94402
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wei-Nchih Lee, MD
Email
wlee@evidation.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Evidence for Health Improvement in People With Diabetes Using One Touch & Partner Solutions

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