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Eat Well Produce Benefit for Diabetes and Food Insecurity

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Duke University

Status

Active, not recruiting

Conditions

Diabetes Mellitus
Food Insecurity

Treatments

Other: Eat Well

Study type

Interventional

Funder types

Other

Identifiers

NCT05896644
Pro00112649

Details and patient eligibility

About

The goal of this clinical trial is to assess the impact of participation in Eat Well for diabetes patients who are at risk of food insecurity. The main questions it aims to answer are:

  • whether there is a difference in Haemoglobin (Hb) A1c measurements and emergency department (ED) utilization between the Eat Well and control groups up to 18 months post-program completion.
  • whether there are differences in cardiometabolic health-related outcomes for Eat Well participants.

Participants in the program will receive gift/debit cards for fruits and vegetables and educational nutrition materials. Researchers will compare Eat Well participants with those only receiving educational materials to see if there are differences in cardiometabolic health outcomes.

Full description

This pragmatic trial aims to assess the impact of Eat Well participation for diabetes patients at risk of food insecurity. Eligible patients will receive gift/debit cards for the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC)-approved fruits and vegetables and be assigned to either receive the card for up to 12 months or not. Random assignment will occur using a 2 to 1 treatment to control allocation ratio. Both treatment and control groups will receive curated diabetes educational materials. The study will assess the impact of the intervention on clinical factors such as glycemic control, weight, BMI, lipids, medication adherence, medication number, blood pressure, and utilization up to 18 months pre, during, and post program enrollment using data from clinical visits. The primary analysis of interest will be differences in HbA1c measurements and ED visits between the Eat Well and control groups at 12 months of program participation, with further evaluation of differences at 12 months post-program completion.

Enrollment

2,177 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Be active in the Duke Diabetes Registry in the past 12 months AND

  • have had at least one outpatient A1c measurement AND

  • are at risk for food insecurity as defined by one of the following:

    1. answered often true or sometimes true on one or both of the food insecurity questions as part of the electronic health record social history section (Maestro Care/ Epic of Verona WI) OR
    2. answered hard or very hard to the financial stress question as part of the electronic health record social history section (Maestro Care/ Epic of Verona WI) OR
    3. has Medicaid as insurance payer OR
    4. lives in Area Deprivation Index (ADI) zip code of 7th decile or harder

Exclusion criteria

  • none

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

2,177 participants in 2 patient groups

Eat Well
Experimental group
Description:
The experimental group will participate in the Eat Well Produce Prescription program, receiving an $80 monthly benefit for eligible produce for 12 months and diabetes education materials through email, including curated nutrition and diet information from the Diabetes Resource Page, consistent with standard of care at Duke University Health System.
Treatment:
Other: Eat Well
Control
No Intervention group
Description:
The control group will receive usual care (including diabetes educational materials) without the prescription benefit.

Trial contacts and locations

1

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Central trial contact

Connor Drake, PhD; Susan Spratt, MD

Data sourced from clinicaltrials.gov

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