Minnesota Medicaid Incentives to Prevent Chronic Disease

Not Applicable

Completed

• Conditions: Prediabetic State

• Registration Number: NCT02422420
• Lead Sponsor: Minnesota Department of Human Services

Brief Summary

The objective of this study is to test whether two different participant financial incentive structures are more effective and cost effective than minimal financial incentives in increasing weight loss among Minnesota Medicaid beneficiaries at high risk of developing diabetes. The incentives are tied to participation and weight loss in the evidence-based group-delivered YMCA diabetes prevention program (Y-DPP). The Investigators will conduct a group randomized trial that includes up to 150 Y-DPP classes of 10-15 participants per class for up to 1500 Medicaid beneficiaries participating in the Y-DPP classes. This approach, if successful, will (a) improve weight loss. diabetes risk, and improve cardiovascular risk among Medicaid beneficiaries at risk for developing diabetes and other chronic conditions, (b) demonstrate that prevention of chronic disease risk factors using patient incentives is cost-effective, and (c) provide a patient incentive model that can be widely used among Medicaid beneficiaries at risk for developing diabetes.

Detailed Description

Not available

Study Timeline

• Study Start: 2013-03
• Study First Submitted: 2015-04-16
• Study First Submitted QC: 2015-04-20
• Study First Posted: 2015-04-21
• Status Verified: 2016-03
• Primary Completion: 2016-09
• Study Completion: 2016-09
• Last Update Submitted: 2016-10-14
• Last Update Posted: 2016-10-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 1500

Inclusion Criteria

• currently enrolled in Medical Assistance, PMAP, or MinnesotaCare (collectively referred to as Medicaid)
• 18-75 years of age
• body mass index ≥ 25 kg/m2 (≥ 22 kg/m2 for those of Asian descent)
• have prediabetes or a history of gestational diabetes mellitus (GDM)

Exclusion Criteria

• diagnosis of diabetes
• pregnant at the time of enrollment
• planning gastric bypass surgery within the next 12 months
• diagnosed with Alzheimer's disease (ICD-9 331.0) or dementia (ICD-9 290.0 - 294.9)
• provider judgment regarding suitability for the study based on substance abuse, uncontrolled mental illness, or other conditions that may affect the participants health or ability to participate in the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
DPP Attendance	12 months	Participation in DPP core and post-core sessions
Weight Change	12 months	Change in participants' weight

Trial Locations

Locations (1)

Minnesota Department of Health; 🇺🇸 St. Paul, Minnesota, United States