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Grocery Prescription Program for Medicaid Adults With Hypertension or Type 2 Diabetes

Grocery Prescription Program for Medicaid Adults With Hypertension or Type 2 Diabetes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06033664
Enrollment
50
Registered
2023-09-13
Start date
2023-11-06
Completion date
2024-05-08
Last updated
2024-05-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 Diabetes Mellitus, Hypertension

Keywords

Food Insecurity, Food as Medicine, Medicaid Adults

Brief summary

The purpose of this study is to evaluate the effectiveness of a grocery prescription program in adults diagnosed with either Type 2 Diabetes Mellitus or Hypertension. Participants will enroll in Instacart Fresh Funds program. Once enrolled each week participants will select foods that are eligible in the Fresh Funds Program to be delivered to their home for 12 weeks. Participants will also participate in a survey at the beginning of the study and at the end of the study.

Interventions

BEHAVIORALFresh Funds

Participants will enroll in Instacart Fresh Funds program. Once enrolled participants will select foods that are eligible in the Fresh Funds to be delivered to their home each week for 12 weeks.

Sponsors

Instacart Health
CollaboratorUNKNOWN
Kentucky Association of Health Plans
CollaboratorUNKNOWN
Alison Gustafson
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of Type 2 Diabetes Mellitus, hemoglobin A1c = 7.0% and = 12.0% in last 12 months, or diagnosis of hypertension * Experiencing food insecurity as indicated by 2-item Hunger Vital Sign * English speaking * No plans to move from the area for at least 1 year * Willing and able to accept text messages * Free living to the extent that participant has control over dietary intake * Willing and able to provide written informed consent and participate in all study activities.

Exclusion criteria

* Participant in diabetes, nutrition, or weight research intervention in last 12 months * Another member of the household is already enrolled in this study * Considering bariatric surgery in the next year or prior bariatric surgery * Lack of safe, stable residence and ability to store meals

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with a percentage change in Hemoglobin A1C (HbgA1C)baseline and post intervention, approximately 12 weeksHbgA1C will be obtained baseline and post intervention by the healthcare provider from the medical chart.

Secondary

MeasureTime frameDescription
Change in blood pressurebaseline and post intervention, approximately 12 weeksBoth systolic and diastolic blood pressure will be obtained baseline and post intervention by the healthcare provider from the medical chart.
Change in food insecuritybaseline and post intervention, approximately 12 weeksThe USDA 6 item food insecurity screener will be used. The scale ranges from 0 to 6 with a higher score indicating greater food insecurity.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026