Living Hungry Healthy Foods Prescription Program
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
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.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Florida
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West Palm Beach, Florida, Estados Unidos, 33401
- Living Hungry
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- 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.
- Diabetic with A1C over 8.0
- Adults 18 years of age or older
- Food-insecure
Exclusion Criteria:
- Referred patients with HbA1c levels below 8.0 mmol/mol
- Minors
- Adults with severe mental illness who cannot provide informed consent, unless they have present a lawful caregiver or power of attorney.
- Anyone who does not plan on staying in West Palm Beach for the next 4 months.
- Pregnant women (can still receive services through the program but will not be included in the analysis)
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Cuidados de apoyo
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Healthy Food Prescription
Participants receive services through the Living Hungry program for food insecure diabetic patients.
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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.
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in Hemoglobin A1c
Periodo de tiempo: pre/post change in HbA1c in participants from baseline to completion of the program at 4 months
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will be measured by blood draws at first and last program event
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pre/post change in HbA1c in participants from baseline to completion of the program at 4 months
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in frequency of hospitalizations
Periodo de tiempo: pre/post change in hospitalizations in participants from baseline to one month after completion of the program
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will be measured through surveys and data from electronic medical records
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pre/post change in hospitalizations in participants from baseline to one month after completion of the program
|
|
Change in frequency of emergency department admissions
Periodo de tiempo: pre/post change in emergency department admissions in participants from baseline to one month after completion of the program
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will be measured through surveys and data from electronic medical records
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pre/post change in emergency department admissions in participants from baseline to one month after completion of the program
|
|
Change in total health care costs
Periodo de tiempo: pre/post change in total health care costs in participants from baseline to one month after completion of the program
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will be measured through data from hospital records
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pre/post change in total health care costs in participants from baseline to one month after completion of the program
|
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Change in food insecurity
Periodo de tiempo: pre/post change in food insecurity in participants from baseline to completion of the program at 4 months
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Food insecurity will be measured using the USDA 9-question food insecurity screener
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pre/post change in food insecurity in participants from baseline to completion of the program at 4 months
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Change in daily servings of fruits and vegetables
Periodo de tiempo: pre/post change in daily servings of fruits and vegetables in participants from baseline to completion of the program at 4 months
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Will be assessed through a food frequency questionnaire modeled off the USDA FINI assessment tool
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pre/post change in daily servings of fruits and vegetables in participants from baseline to completion of the program at 4 months
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Change in daily servings of whole grains
Periodo de tiempo: pre/post change in daily servings of whole grains in participants from baseline to completion of the program at 4 months
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Will be assessed through a food frequency questionnaire modeled off the USDA FINI assessment tool
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pre/post change in daily servings of whole grains in participants from baseline to completion of the program at 4 months
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Change in daily servings of lean proteins
Periodo de tiempo: pre/post change in daily servings of lean proteins in participants from baseline to completion of the program at 4 months
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Will be assessed through a food frequency questionnaire modeled off the USDA FINI assessment tool and includes: nuts, seeds, legumes, poultry, and fish.
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pre/post change in daily servings of lean proteins in participants from baseline to completion of the program at 4 months
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Change in daily servings of sugary snacks and drinks
Periodo de tiempo: pre/post change in daily servings of sugary snacks and drinks in participants from baseline to completion of the program at 4 months
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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
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pre/post change in daily servings of sugary snacks and drinks in participants from baseline to completion of the program at 4 months
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Change in medication adherence
Periodo de tiempo: pre/post change in medication adherence in participants from baseline to completion of the program at 4 months
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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.
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pre/post change in medication adherence in participants from baseline to completion of the program at 4 months
|
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Change in adhering to recommended diabetes management plan
Periodo de tiempo: pre/post change in in adhering to recommended diabetes management in participants from baseline to completion of the program at 4 months
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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.
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pre/post change in in adhering to recommended diabetes management in participants from baseline to completion of the program at 4 months
|
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Change in blood LDL level
Periodo de tiempo: pre/post change in systolic blood LDL levels in participants from baseline to completion of the program at 4 months
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measured at first and last program event through a blood draw
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pre/post change in systolic blood LDL levels in participants from baseline to completion of the program at 4 months
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Change in systolic blood pressure
Periodo de tiempo: pre/post change in systolic blood pressure in participants from baseline to completion of the program at 4 months
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measured at first and last program event
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pre/post change in systolic blood pressure in participants from baseline to completion of the program at 4 months
|
|
Change in diastolic blood pressure
Periodo de tiempo: pre/post change in diastolic blood pressure in participants from baseline to completion of the program at 4 months
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measured at first and last program event
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pre/post change in diastolic blood pressure in participants from baseline to completion of the program at 4 months
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Dariush Mozaffarian, MD, DrPH, Tufts University Friedman School of Nutrition Science and Policy
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- 13491
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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