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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03369626
Other study ID # dmstudyv4
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 26, 2017
Est. completion date February 28, 2018

Study information

Verified date August 2019
Source FareWell
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 118
Est. completion date February 28, 2018
Est. primary completion date January 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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)

Study Design


Intervention

Behavioral:
FareWell Program
The FareWell Program is a digitally delivered lifestyle management curriculum, which includes meal planning tools, daily self monitoring, personalized goal setting and bi-weekly live one-on-one health coaching.

Locations

Country Name City State
United States FareWell LLC San Francisco California

Sponsors (1)

Lead Sponsor Collaborator
FareWell

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Level of engagement with the assigned mobile app How do participants interact with the digital program (e.g. feature use, coaching calls completed, targets tracked, targets met) 12 weeks
Secondary Change in self-reported Hemoglobin A1c Comparison of baseline and end program self reported Hemoglobin A1c 12 weeks
Secondary Change in self-reported diabetes medication type or dose Comparison of diabetes medications reported at baseline to any changes reported at the end of the study or mid-study 12 weeks
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