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Pathway for Produce Prescriptions in Diabetes Management

Multi-level Evaluation of Produce Prescription Projects on Type 2 Diabetes-related Outcomes: A Pathway to Policy Change by Addressing Social Determinants of Health

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06058338
Acronym
PPT2D
Enrollment
600
Registered
2023-09-28
Start date
2023-05-31
Completion date
2024-08-30
Last updated
2023-10-05

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

Conditions

Type 2 Diabetes

Keywords

Produce Prescriptions, Social Determinants of Health, Food Security

Brief summary

Fruit and vegetable (FV) intake decrease the risk of type 2 diabetes (T2D) and is important for T2D management but is difficult to achieve in adequate amounts for those with a low- income. Produce Prescription (PPR) projects are an intervention aligned with the social determinants of health that help individuals with a low-income purchase FV by providing an incentive. The impacts of PPR projects on populations with T2D and a low-income is less understood. The Multi-level evaluation of Produce Prescription Projects on type 2 diabetes- related outcomes: A pathway to policy change by addressing social determinants of health study will determine the impact of PPR projects on hemo-globin A1c (HbA1c; primary outcome), fruit and vegetable intake (FVI), food security, and related behaviors among a diverse sample of PPR participants diagnosed with T2D and low-income (Aim 1), and will conduct a cost and cost-effective analysis of PPR projects (Aim 2), and a mixed methods process evaluation to understand feasibility and best practices for PPR projects for people with/at risk for T2D (Aim 3). We hypothesize that PPR participants will see greater declines in HbA1c and improvements in other health and food-related behaviors, compared to the Standard of Care. We will recruit five GusNIP PPR projects, whose healthcare partners serve patients with T2D, and who have participating and matched non-participating control populations. We will collect data at baseline and post-intervention using validated, survey modules, clinical measures, and cost data. Five types of data will be used for this project: 1.Health and healthcare utilization data from the EHR or point-of-care, 2.Participant survey data, 3.Qualitative data, 4.Program cost data (NOT human subjects), and 5.Process data (NOT human subjects). Information extracted from medical records includes HbA1c, weight, and blood pressure and will be collected at 2 time points (months 0,6), following their standard of care protocols. Staff will also extract healthcare utilization data (e.g., #primary care and #ER visits) from the EHR at each of site. Primary analyses will use an intention to treat strategy. Analysis will include a linear mixed-effect model to the HbA1c with an interaction between group and time to examine whether there is a difference in HbA1c trajectories between intervention and control groups. Similar models will be used to determine impact on each of the secondary outcomes (e.g., healthcare utilization, BMI).

Interventions

Produce prescriptions mitigate health and food access inequities by partnering with healthcare providers to prescribe fruits and vegetables via financial incentives to patients experiencing food insecurity, low income, and/or chronic disease(s) risk.

Sponsors

American Diabetes Association
CollaboratorOTHER
University of Colorado, Denver
CollaboratorOTHER
University of California, San Francisco
CollaboratorOTHER
Children's Hospital Medical Center, Cincinnati
CollaboratorOTHER
Lawndale Christian Health Center
CollaboratorOTHER
Virtua Health
CollaboratorOTHER
Parkview Hospital, Indiana
CollaboratorOTHER
Presbyterian Healthcare Services
CollaboratorUNKNOWN
Market Umbrella
CollaboratorUNKNOWN
Gretchen Swanson Center for Nutrition
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

1. diagnosed with Type 2 diabetes 2. have clinically screened positive for food insecurity and/or be income-eligible to receive Medicaid and/or SNAP-benefits 3. ≥ 18 years of age, and 4. be a patient at a participating healthcare site.

Exclusion criteria

1. people who pregnant or nursing and 2. plans to move away during the study period.

Design outcomes

Primary

MeasureTime frameDescription
Hemoglobin A1cMonths 0,6Participant HbA1c will be collected by point-of-care venipuncture or from lab draws in electronic medical records.

Secondary

MeasureTime frameDescription
Body Mass IndexMonths 0,6Participant BMI will be calculated from height/weight measurements from electronic medical records.
Blood pressureMonths 0,6Participant systolic and diastolic blood pressure measurements will be collected from electronic medical records.
Fruit and vegetable intakeMonths 0,6Participant fruit and vegetable intake as measured by the NCI/NIH Dietary Screener Questionnaire (DSQ) 10-item fruit and vegetable module.
Food securityMonths 0,6Participant food security status as measured by the USDA 6-item food security survey.
Diabetes distressMonths 0,6Participant diabetes distress as measured by the Problem Areas in Diabetes Scale (PAID-5) using the scale of 0, not a problem, to 4, serious problem with higher scores indicating more emotional stress from living with diabetes
Health-related Quality of LifeMonths 0,6Participant health-related quality of life as measured by the Short Form (SF)-12 module that addresses 8 domains of physical and mental health along a scale ranging from 0 to 100, with higher scores indicating better physical and mental health functioning
Self-efficacyMonths 0,6Participant self-efficacy for eating fruits and vegetables as measured by a single survey question using a 5 point scale from 0 to 5 with 0 indicating not at all confident and 5 indicating very confident.
Self-reported healthMonths 0,6Participant self-reported health status as measured by a single survey question using a 5 point scale from 0 to 5 with 0 indicating poor health and 5 indicating excellent health
Program satisfactionMonth 6Participant produce prescription program satisfaction as measured by a single survey question using a 5 point scale from 0 to 5 with 0 indicating very negative satisfaction and 5 indicating very positive satisfaction

Other

MeasureTime frameDescription
Program feasibilityMonths 1-2, 7-8A process evaluation measure for the feasibility of produce prescription programs as measured by interviews with key partners.
Program costMonths 1-6The estimated cost to operate a produce prescription program for four-to-six months as measured by clinic administrative records and staff interviews.
Cost-effectiveness (HbA1c -1%)Months 0-6The cost-effectiveness of produce prescription program on a 1% decrease in HbA1c over four-to-six months as measured by clinic administrative records and staff interviews (combines outcome 1 and outcome 11).
FidelityMonths 1-6A process evaluation measure for how well intervention components were delivered according to plan (e.g., number of nutrition educational activities delivered compared to the number scheduled) as measured by clinic administrative records and semi-structured interviews.
Cost-effectiveness (HbA1c <7%)Months 0-6The cost-effectiveness of produce prescription program on reducing HbA1c to \<7% among participants with HbA1c \>=7% as measured by clinic administrative records and staff interviews (combines outcome 1 and outcome 11).
Program reachMonths 1-6A process evaluation measure for the proportion of intervention group participants that received at least one produce prescription incentive as measured by clinic administrative records.
Dose deliveredMonths 1-6A process evaluation measure for the percentage of intended intervention components delivered to participants (e.g., dollar amount and frequency of prescriptions issued) as measured by clinic administrative records.
Dose receivedMonths 1-6A process evaluation measure for the percentage of intended intervention components received by participants (e.g., number of nutrition education activities attended) as measured by clinic administrative records.
Participant experiencesMonths 7-8A process evaluation measure for participant experience with the produce prescription as measured by participant focus groups.

Countries

United States

Outcome results

None listed

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