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Eat Well Produce Benefit for Diabetes and Food Insecurity

Primary Purpose

Diabetes Mellitus, Food Insecurity

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Eat Well
Sponsored by
Duke University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept 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: 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 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 has Medicaid as insurance payer OR lives in Area Deprivation Index (ADI) zip code of 7th decile or harder Exclusion Criteria: none

Sites / Locations

  • Duke University Health SystemRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Eat Well

Control

Arm 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.

The control group will receive usual care (including diabetes educational materials) without the prescription benefit.

Outcomes

Primary Outcome Measures

Change in HbA1C
A measure of average blood sugar levels over the past 3 months.
Change in number of ED Visits
Number of ED visits throughout the study period

Secondary Outcome Measures

Outpatient visits
Number of outpatient visits during the study period
Hospitalizations
Number of patient hospitalizations during the study period
Change in weight
Change in body mass index (BMI)
A measure of body fat based on height and weight.
Change in cholesterol
Measure of lipids
Medication adherence (proportion of days covered)
Medication adherence will be measured by linking EHR data with Surescripts e-prescription network data. Surescripts facilitates medication refill information exchange between healthcare organizations and pharmacies. Adherence will be calculated using the proportion of days covered (PDC) approach
Change in number of diabetes and hypertension medications
Change in diabetes and hypertension medication numbers
Change in blood pressure
Systolic and Diastolic blood pressure

Full Information

First Posted
May 26, 2023
Last Updated
June 23, 2023
Sponsor
Duke University
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1. Study Identification

Unique Protocol Identification Number
NCT05896644
Brief Title
Eat Well Produce Benefit for Diabetes and Food Insecurity
Official Title
An Evaluation of Eat Well, a Produce Benefit, for Patients With Diabetes and At-risk for Food Insecurity
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 20, 2023 (Actual)
Primary Completion Date
June 2024 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke 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
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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Food Insecurity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
3000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Eat Well
Arm Type
Experimental
Arm 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.
Arm Title
Control
Arm Type
No Intervention
Arm Description
The control group will receive usual care (including diabetes educational materials) without the prescription benefit.
Intervention Type
Other
Intervention Name(s)
Eat Well
Intervention Description
A program offered by Reinvestment Partners giving clients gift/debit cards that allow the purchase of WIC approved fruits and vegetables.
Primary Outcome Measure Information:
Title
Change in HbA1C
Description
A measure of average blood sugar levels over the past 3 months.
Time Frame
18 months pre program, during program enrollment, and up to 18 months post program
Title
Change in number of ED Visits
Description
Number of ED visits throughout the study period
Time Frame
up to 18 months pre program, during program, and up to 18 months post program enrollment
Secondary Outcome Measure Information:
Title
Outpatient visits
Description
Number of outpatient visits during the study period
Time Frame
up to 18 months pre program, during program, and up to 18 months post program enrollment
Title
Hospitalizations
Description
Number of patient hospitalizations during the study period
Time Frame
up to 18 months pre program, during program, and up to 18 months post program enrollment
Title
Change in weight
Time Frame
up to 18 months pre program, during program, and up to 18 months post program enrollment
Title
Change in body mass index (BMI)
Description
A measure of body fat based on height and weight.
Time Frame
up to 18 months pre program, during program, and up to 18 months post program enrollment
Title
Change in cholesterol
Description
Measure of lipids
Time Frame
up to 18 months pre program, during program, and up to 18 months post program enrollment
Title
Medication adherence (proportion of days covered)
Description
Medication adherence will be measured by linking EHR data with Surescripts e-prescription network data. Surescripts facilitates medication refill information exchange between healthcare organizations and pharmacies. Adherence will be calculated using the proportion of days covered (PDC) approach
Time Frame
up to 18 months pre program, during program, and up to 18 months post program enrollment
Title
Change in number of diabetes and hypertension medications
Description
Change in diabetes and hypertension medication numbers
Time Frame
up to 18 months pre program, during program, and up to 18 months post program enrollment
Title
Change in blood pressure
Description
Systolic and Diastolic blood pressure
Time Frame
up to 18 months pre program, during program, and up to 18 months post program enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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: 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 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 has Medicaid as insurance payer OR lives in Area Deprivation Index (ADI) zip code of 7th decile or harder Exclusion Criteria: none
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Connor Drake, PhD
Phone
+1 919 724 2129
Email
connor.drake@duke.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Susan Spratt, MD
Phone
+1 919 668 5360
Email
susan.spratt@duke.edu
Facility Information:
Facility Name
Duke University Health System
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27708
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Connor Drake, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Access to all participant data and information will be restricted to authorized personnel. Internal monitoring of data may occur as required by Duke for investigator-initiated clinical research.
Links:
URL
http://diabetes.my.dukehealth.org
Description
Resource guide to be provided to all patients, regardless of selection in intervention or control group
URL
https://nf01.diabeteseducator.org/eweb/DynamicPage.aspx?Site=aade&WebCode=DEAPFindApprovedProgram
Description
Link provided to all patients to find diabetes self management education and support in their area

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Eat Well Produce Benefit for Diabetes and Food Insecurity

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