Evaluation of Prevent in Underserved Populations



Status:Completed
Conditions:Obesity Weight Loss, Endocrine, Diabetes
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:18 - 75
Updated:8/23/2018
Start Date:January 2016
End Date:May 2018

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Evaluation of an Online Diabetes Prevention Program Adapted for Safety Net Users

The goal of this study is to evaluate an online Diabetes Prevention Program adapted for
patients with prediabetes in safety net health care settings.

The Diabetes Prevention Program (DPP) demonstrated that intensive behavioral counseling is a
successful approach to reduce the risk of developing diabetes in patients with prediabetes.
While the DPP lifestyle intervention was successful and group based adaptations of the DPP
have positive results, scalable alternatives that allow for even broader reach are necessary.
Omada Health has developed an online, group-based, recognized DPP program (Prevent). The goal
of this study is to evaluate a literacy-adapted version of Prevent for patients with
prediabetes in safety net health care settings.

Inclusion Criteria:

- is receiving care at one of the three participating locations

- prediabetes diagnosis confirmed by lab tests

- age 18-75 at screening

- Not insured, Medicaid insured, or safety net health plan insured

- Comfortable speaking/reading English or Spanish at 5th grade level

- Body Mass Index greater or equal to 24

- Able to access the internet weekly by computer or smartphone

- Able to engage in physical activity of at least moderate intensity

- Able and willing to give informed consent to participate

Exclusion Criteria:

- diagnosed with Type 1 or 2 Diabetes Mellitus

- taking insulin, metformin or other hypoglycemic agent

- pregnant or planning to become pregnant during trial period

- unstable life conditions that would preclude full program participation

- acute, unstable medical or mental health conditions that would preclude program
participation

- inability to engage in physical activity of at least moderate intensity
We found this trial at
3
sites
Monroe, Washington 98272
Principal Investigator: Wendy Imberg, ARNP, PhD
Phone: 360-805-3926
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Los Angeles, California 90033
Principal Investigator: Barbara Rubino, MD
Phone: 213-784-9191
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Los Angeles, CA
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San Fernando, California 91340
Principal Investigator: Debra Rosen, RN, MPH
Phone: 818-403-1576
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San Fernando, CA
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