Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
227 participants
INTERVENTIONAL
2016-01-31
2018-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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online Diabetes Prevention Program
Participants will receive access to a 12-month online diabetes prevention program modeled after the CDC DPP curriculum. Participants receive online curriculum, access to a live health coach, interactive group message forums, and connected weight and activity monitoring devices.
Prevent
Intensive behavioral counseling for diabetes prevention and healthy lifestyle management. Recipients have access to online curriculum, a live health coach, group-based communication forums, and connected technology to track weight and physical activity.
Matched Control
A de-identified dataset of control subjects matched on age, gender, prediabetes diagnosis, body mass index, comorbidities and socioeconomic status will be cultivated for comparison to the active intervention arm.
No interventions assigned to this group
Interventions
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Prevent
Intensive behavioral counseling for diabetes prevention and healthy lifestyle management. Recipients have access to online curriculum, a live health coach, group-based communication forums, and connected technology to track weight and physical activity.
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
75 Years
ALL
Yes
Sponsors
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Kresge Foundation
UNKNOWN
California HealthCare Foundation
OTHER
University of Southern California
OTHER
Omada Health, Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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Michael R Cousineau, DrPh
Role: PRINCIPAL_INVESTIGATOR
University of Southern California
Locations
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LAC+USC Medical Center
Los Angeles, California, United States
Northeast Valley Health Corporation
San Fernando, California, United States
Providence Medical Group-Monroe Clinic
Monroe, Washington, United States
Countries
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Related Links
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Omada is a San Francisco-based healthcare technology company that is pioneering the field of digital behavioral medicine, to fulfill our mission of inspiring and enabling people everywhere to live free of chronic disease.
Other Identifiers
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WIRB20152184
Identifier Type: -
Identifier Source: org_study_id
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