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Prevention of Diabetes Using Mobile-enabled, Virtual Delivery of the National Diabetes Prevention Program

Primary Purpose

PreDiabetes

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Noom Coach DPP
Sponsored by
Noom Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for PreDiabetes focused on measuring mHealth, Diabetes Prevention Program, weight loss, body weight, behavioral interventions

Eligibility Criteria

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

Inclusion criteria:

  • English-speaking
  • 18 years of age and older
  • Referral from the patient's physician
  • Hemoglobin A1C: 5.7 - 6.4 within the 3 months prior to enrollment
  • Own a smartphone (Apple or Android)

Exclusion criteria:

  • Recent weight loss (by patient report, >5 lbs in the 6 months preceding enrollment visit)
  • previous diagnosis of type 1 or type 2 diabetes
  • serious or persistent mental illnesses
  • more than 72 hours of hospitalization in the last 30 days
  • Enrollment in a structured weight-loss program currently or within the 1 month preceding study enrollment
  • Pregnant
  • Currently nursing
  • Have given birth within the past 3 months
  • Has been discouraged by a physician to enroll in a DPP program

Sites / Locations

  • Stony Brook University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Noom Coach DPP

Usual Care

Arm Description

Individuals will receive special instructions on how to use the app and will self-monitor their weight, exercise and receive daily DPP core content through the app over 16 weeks plus guidance from a coach, and will thereafter receive post-core DPP content up to 52 weeks.

The control group will be a "usual care" condition in which participants are free to seek any assistance for their medical care during the study period plus a paper version of the DPP curriculum.

Outcomes

Primary Outcome Measures

Change in weight
Body weight recorded during follow-up appointments at the medical clinic.

Secondary Outcome Measures

Change in hemoglobin A1c
Hemoglobin A1c measured during follow-up appointments at the medical clinic.

Full Information

First Posted
March 4, 2019
Last Updated
April 4, 2023
Sponsor
Noom Inc.
Collaborators
Stony Brook University
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1. Study Identification

Unique Protocol Identification Number
NCT03865342
Brief Title
Prevention of Diabetes Using Mobile-enabled, Virtual Delivery of the National Diabetes Prevention Program
Official Title
Prevention of Diabetes Using Mobile-enabled, Virtual Delivery of the National Diabetes Prevention (DPP) Program: a Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
September 2016 (Actual)
Primary Completion Date
June 25, 2018 (Actual)
Study Completion Date
June 25, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Noom Inc.
Collaborators
Stony Brook University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will test the weight loss efficacy of a mobile diabetes prevention program intervention. Half of the sample of prediabetic adults will receive the virtual DPP and half will receive usual medical care.
Detailed Description
There were 84.1 million people with pre-diabetes, 30.3 million people with diagnosed and 7.2 million with undiagnosed diabetes in the United States in 2015, and nearly 2 million are diagnosed with it every year. By 2050, the CDC estimates that 1 in every 3 people globally will have diabetes, a leading cause of death and disability. The primary goal of this study is to evaluate the efficacy of the Noom Coach Diabetes Prevention Program mobile platform versus usual medical care. The best intervention to date for prediabetes is the Centers for Disease Control and Prevention's Diabetes Prevention Program, yet there is limited research investigating a mobile-based delivery of the DPP. Pre-diabetes is often discovered during routine medical visitation/annual screening (usual care), but face-to-face time with clinicians is often limited. Exploring novel ways, such as mHealth interventions to empower patients to pursue lifestyle change and prevent or delay diabetes onset is critical to addressing the growing diabetes epidemic.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
PreDiabetes
Keywords
mHealth, Diabetes Prevention Program, weight loss, body weight, behavioral interventions

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
202 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Noom Coach DPP
Arm Type
Experimental
Arm Description
Individuals will receive special instructions on how to use the app and will self-monitor their weight, exercise and receive daily DPP core content through the app over 16 weeks plus guidance from a coach, and will thereafter receive post-core DPP content up to 52 weeks.
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
The control group will be a "usual care" condition in which participants are free to seek any assistance for their medical care during the study period plus a paper version of the DPP curriculum.
Intervention Type
Behavioral
Intervention Name(s)
Noom Coach DPP
Intervention Description
Subjects receiving the smartphone app will receive the DPP core curriculum for 16 weeks and then the post-core curriculum for 36 weeks through the app. The Noom mobile app allows secure patient monitoring through a participant dashboard that the coach can use to increase patient adherence and motivation to achieve DPP goals. The participant can log their food intake, weight, steps, exercise, in addition to participating in the DPP group interaction through the application.
Primary Outcome Measure Information:
Title
Change in weight
Description
Body weight recorded during follow-up appointments at the medical clinic.
Time Frame
Baseline, 6, and 12 months
Secondary Outcome Measure Information:
Title
Change in hemoglobin A1c
Description
Hemoglobin A1c measured during follow-up appointments at the medical clinic.
Time Frame
Baseline, 6, and 12 months
Other Pre-specified Outcome Measures:
Title
Change in work productivity
Description
Work Productivity and Activity Impairment Questionnaire: General Health V2.0 (WPAI) Are you currently employed (working for pay)? During the past seven days, how many hours did you miss from work because of your health problems? During the past seven days, how many hours did you miss from work because of any other reason, such as vacation, holidays, time off to participate in this study? During the past seven days, how many hours did you actually work? During the past seven days, how much did your health problems affect your productivity while you were working? (0-10, higher is more impact) During the past seven days, how much did your health problems affect your ability to do your regular daily activities, other than work at a job? By regular activities, we mean the usual activities you do, such as work around the house, shopping, childcare, exercising, studying, etc.(0-10, higher is more impact)
Time Frame
Baseline, 6, and 12 months
Title
Change in quality of life
Description
Healthy Days Core Module (CDC HRQOL- 4) Would you say that in general your health is excellent, very good, good, fair or poor? Excellent Good Fair Poor Now thinking about your physical health, which includes physical illness and injury, how many days during the past 30 days was your physical health not good? Now thinking about your mental health, which includes stress, depression, and problems with emotions, how many days during the past 30 days was your mental health not good? During the past 30 days, approximately how many days did poor physical or mental health keep you from doing your usual activities, such as self-care, work, or recreation?
Time Frame
Baseline, 6, and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: English-speaking 18 years of age and older Referral from the patient's physician Hemoglobin A1C: 5.7 - 6.4 within the 3 months prior to enrollment Own a smartphone (Apple or Android) Exclusion criteria: Recent weight loss (by patient report, >5 lbs in the 6 months preceding enrollment visit) previous diagnosis of type 1 or type 2 diabetes serious or persistent mental illnesses more than 72 hours of hospitalization in the last 30 days Enrollment in a structured weight-loss program currently or within the 1 month preceding study enrollment Pregnant Currently nursing Have given birth within the past 3 months Has been discouraged by a physician to enroll in a DPP program
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joshua D Miller, MD, MPH
Organizational Affiliation
Stony Brook University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stony Brook University
City
Stony Brook
State/Province
New York
ZIP/Postal Code
11794
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32459631
Citation
Toro-Ramos T, Michaelides A, Anton M, Karim Z, Kang-Oh L, Argyrou C, Loukaidou E, Charitou MM, Sze W, Miller JD. Mobile Delivery of the Diabetes Prevention Program in People With Prediabetes: Randomized Controlled Trial. JMIR Mhealth Uhealth. 2020 Jul 8;8(7):e17842. doi: 10.2196/17842.
Results Reference
derived

Learn more about this trial

Prevention of Diabetes Using Mobile-enabled, Virtual Delivery of the National Diabetes Prevention Program

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