Living Hungry Healthy Foods Prescription Program

Sponsor
Tufts University (Other)
Overall Status
Completed
CT.gov ID
NCT04205617
Collaborator
Health Care District of Palm Beach County (Other), South Florida Hunger Coalition (Other), Jupiter Medical Center (Other), MyClinic, Inc (Other), FoundCare Inc. (Other), Living Hungry, Inc. (Other)
35
1
1
10
3.5

Study Details

Study Description

Brief Summary

This study is a pre/post, pilot evaluation of the 4-month, Living Hungry program for food-insecure patients with uncontrolled diabetes. The program provides free produce, whole grains and legumes to participants and their household every-other week, in addition, to nutrition education and glucose monitoring devices. The study is analyzing diabetes management indicators, including HbA1c, dietary quality, food insecurity, and medication adherence, plus health care utilization.

Condition or Disease Intervention/Treatment Phase
  • Other: produce prescription and nutrition education
N/A

Detailed Description

The Living Hungry Collaborative, in partnership with the South Florida Hunger Coalition, previously operated a pilot program, Fresh Food Farmacy, staged from June 1, 2018, to September 29, 2018. The program consisted of nine Eat Well Pop-Up Pantry events at the My Clinic in Jupiter, Florida, serving 104 patients and feeding approximately 300 people including their families. Each set of groceries contained two weeks' worth of "medically tailored" groceries for diabetic-friendly meals for food-insecure patients diagnosed with diabetes or prediabetes. All clients involved in the intervention were referred by staff at the same four clinics that will participate in this study: My Clinic, C.L. Brumback Clinic in Jupiter, Jupiter Medical Center, and FoundCare. The Living Hungry Collaborative has an ongoing program to further evolve and test the "Fresh Food Farmacy", renamed as the Healthy Food Prescription Program intervention in Palm Beach County, for food-insecure, diabetic patients.

In addition to receiving diabetic appropriate groceries at the former Fresh Food Farmacy events, clients will be engaged in diabetes education classes led by volunteer doctors and nurses, cooking demonstrations, shared meals, 1:1 and group coaching by nutritionists and dietitians on best choices from a menu for diabetics, and tasting new recipes with produce from the pop-up event. The pilot program allowed Living Hungry to fine-tune the patient referral process, distribution logistics, and establish strong partnerships required for the next phase of the program. However, gaps exist to understand the extent to which the program design is improving the health of the participating diabetic patients.

Living Hungry will partner with Tufts University to conduct an evaluation of this existing program on key health outcomes that concern the partner clinics, specifically: biomarkers including Hemoglobin A1C, BMI, blood pressure, lipid profile, health care utilization including medication use, hospitalizations, emergency department visits, and health care costs, plus dietary quality, food insecurity, medication use, and quality of life indicators. The study is a pilot evaluation, implementing a quasi-experimental, pre/post study design.

The Living Hungry Healthy Foods Prescription Program is a community-based program that will be available to individuals whether or not they participate in the evaluation by Tufts University. This program is using the same referral and data collections procedures as the pilot, which include having physicians at the partner clinics refer patients with HbA1C levels greater than 8.0 mmol/mol and who are food insecure to Living Hungry to participate in the program. In addition, Living Hungry will again collect data on HbA1c, BMI, blood pressure, lipid profiles, and distribute a survey to participants.

Study Design

Study Type:
Interventional
Actual Enrollment :
35 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Pre/post quasi experimentalPre/post quasi experimental
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Living Hungry Healthy Foods Prescription Program
Actual Study Start Date :
Dec 14, 2019
Actual Primary Completion Date :
Jul 25, 2020
Actual Study Completion Date :
Oct 13, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Healthy Food Prescription

Participants receive services through the Living Hungry program for food insecure diabetic patients.

Other: produce prescription and nutrition education
Participants will receive diabetic appropriate groceries, diabetes education classes led by volunteer doctors and nurses, cooking demonstrations, shared meals, 1:1 and group coaching by dietitians.
Other Names:
  • medically tailored food
  • Outcome Measures

    Primary Outcome Measures

    1. Change in Hemoglobin A1c [pre/post change in HbA1c in participants from baseline to completion of the program at 4 months]

      will be measured by blood draws at first and last program event

    Secondary Outcome Measures

    1. Change in frequency of hospitalizations [pre/post change in hospitalizations in participants from baseline to one month after completion of the program]

      will be measured through surveys and data from electronic medical records

    2. Change in frequency of emergency department admissions [pre/post change in emergency department admissions in participants from baseline to one month after completion of the program]

      will be measured through surveys and data from electronic medical records

    3. Change in total health care costs [pre/post change in total health care costs in participants from baseline to one month after completion of the program]

      will be measured through data from hospital records

    4. Change in food insecurity [pre/post change in food insecurity in participants from baseline to completion of the program at 4 months]

      Food insecurity will be measured using the USDA 9-question food insecurity screener

    5. Change in daily servings of fruits and vegetables [pre/post change in daily servings of fruits and vegetables in participants from baseline to completion of the program at 4 months]

      Will be assessed through a food frequency questionnaire modeled off the USDA FINI assessment tool

    6. Change in daily servings of whole grains [pre/post change in daily servings of whole grains in participants from baseline to completion of the program at 4 months]

      Will be assessed through a food frequency questionnaire modeled off the USDA FINI assessment tool

    7. Change in daily servings of lean proteins [pre/post change in daily servings of lean proteins in participants from baseline to completion of the program at 4 months]

      Will be assessed through a food frequency questionnaire modeled off the USDA FINI assessment tool and includes: nuts, seeds, legumes, poultry, and fish.

    8. Change in daily servings of sugary snacks and drinks [pre/post change in daily servings of sugary snacks and drinks in participants from baseline to completion of the program at 4 months]

      Will be assessed through a food frequency questionnaire modeled off the USDA FINI assessment tool and includes: sugar sweetened beverages, pastries, cookies, cakes, candy, and other sweets

    9. Change in medication adherence [pre/post change in medication adherence in participants from baseline to completion of the program at 4 months]

      Measured as a composite score that will be assessed through a survey. Components include: frequency of sacrificing medication purchases for other household needs (such as food, utilities) and change in medication use.

    10. Change in adhering to recommended diabetes management plan [pre/post change in in adhering to recommended diabetes management in participants from baseline to completion of the program at 4 months]

      Measured as a composite scale that will be assessed through a survey. Components include frequency in which participants followed the recommendations of their physicians to manage their diabetes.

    11. Change in blood LDL level [pre/post change in systolic blood LDL levels in participants from baseline to completion of the program at 4 months]

      measured at first and last program event through a blood draw

    12. Change in systolic blood pressure [pre/post change in systolic blood pressure in participants from baseline to completion of the program at 4 months]

      measured at first and last program event

    13. Change in diastolic blood pressure [pre/post change in diastolic blood pressure in participants from baseline to completion of the program at 4 months]

      measured at first and last program event

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Referred patient from one of four medical partners: My Clinic, C.L. Brumback Clinic, FoundCare and Jupiter Medical Center and has been a patient for at least one-year.

    2. Diabetic with A1C over 8.0

    3. Adults 18 years of age or older

    4. Food-insecure

    Exclusion Criteria:
    1. Referred patients with HbA1c levels below 8.0 mmol/mol

    2. Minors

    3. Adults with severe mental illness who cannot provide informed consent, unless they have present a lawful caregiver or power of attorney.

    4. Anyone who does not plan on staying in West Palm Beach for the next 4 months.

    5. Pregnant women (can still receive services through the program but will not be included in the analysis)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Living Hungry West Palm Beach Florida United States 33401

    Sponsors and Collaborators

    • Tufts University
    • Health Care District of Palm Beach County
    • South Florida Hunger Coalition
    • Jupiter Medical Center
    • MyClinic, Inc
    • FoundCare Inc.
    • Living Hungry, Inc.

    Investigators

    • Principal Investigator: Dariush Mozaffarian, MD, DrPH, Tufts University Friedman School of Nutrition Science and Policy

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Dariush Mozaffarian, Dean - Friedman School, Tufts University
    ClinicalTrials.gov Identifier:
    NCT04205617
    Other Study ID Numbers:
    • 13491
    First Posted:
    Dec 19, 2019
    Last Update Posted:
    Oct 28, 2020
    Last Verified:
    Oct 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Dariush Mozaffarian, Dean - Friedman School, Tufts University

    Study Results

    No Results Posted as of Oct 28, 2020