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Clinical Trials/NCT03369626
NCT03369626
Completed
Not Applicable

Effectiveness of a Digital Therapeutic in a Geographically Distributed Population With Type 2 Diabetes

FareWell1 site in 1 country118 target enrollmentJuly 26, 2017
ConditionsType2 Diabetes

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Type2 Diabetes
Sponsor
FareWell
Enrollment
118
Locations
1
Primary Endpoint
Level of engagement with the assigned mobile app
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

A clinical study evaluating a three month digitally delivered lifestyle change program in adults with Type 2 Diabetes. The FareWell Program (the "Program") aims to reduce well-established biomarkers of cardiometabolic diseases, weight, and medications. The current study is designed to evaluate to what degree adults with Type 2 Diabetes engaged with the Program can improve glycemic control and/or decrease medication needs.

Detailed Description

The Program aims to reduce well-established biomarkers of cardiometabolic diseases, weight, and medications. It includes meal planning tools, smart shopping lists, recipes curated by a physician, dietitian and chef educator, daily self-monitoring features with personalized weekly goals, bi-weekly live one-on-one health coaching and support from an online member community, and an educational curriculum. Subjects in the Program may receive support from other members of a Care Team (lifestyle medicine physician, chef educator, registered dietitian and/or psychologist/psychiatrist) as needed. The Care Team does not provide medical advice, nor replace traditional medical care. Instead, the Care Team encourages behavior change by providing support and sharing its expertise. Study participants will have access to the Program for a twelve week period and will be asked to complete short health surveys at baseline and at the end of the study.

Registry
clinicaltrials.gov
Start Date
July 26, 2017
End Date
February 28, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
FareWell
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • diagnosis of type 2 diabetes

Exclusion Criteria

  • Inability to understand, consent to, or comply with the study protocol for any reason, including inability to read or comprehend English.
  • Does not have a smartphone (either an iPhone or Android phone)

Outcomes

Primary Outcomes

Level of engagement with the assigned mobile app

Time Frame: 12 weeks

How do participants interact with the digital program (e.g. feature use, coaching calls completed, targets tracked, targets met)

Secondary Outcomes

  • Change in self-reported Hemoglobin A1c(12 weeks)
  • Change in self-reported diabetes medication type or dose(12 weeks)

Study Sites (1)

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