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Food As Medicine Study

Primary Purpose

Diabetes Mellitus, Type 2

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Produce prescription (weekly produce delivery)
Sponsored by
Kaiser Permanente
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 years of age or older
  • Diagnosed with Type 2 Diabetes for at least 24 months
  • Diagnosed with Type 2 Diabetes and have at least two HbA1cs of 7.5% or higher in 12 months prior to recruitment
  • Have MediCaid insurance at the time of their last hba1c test
  • Will be able to provide informed consent
  • Will be able to consent to research activities, including receiving a weekly produce box
  • Will be able to receive and prepare delivered foods

Exclusion Criteria:

  • Pregnant women
  • Living in a board and care where your meals are provided for you
  • Unable to provide informed consent

Sites / Locations

  • Kaiser Permanente Southern California

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

No Intervention

Arm Label

Intervention- High Dose

Intervention-Low Dose

Usual Care

Arm Description

Participation will last approximately 6 months. Participants enrolled in the high-dose intervention arm will receive a weekly produce delivery directly to their home in addition to the completion of 3 questionnaires and collection of the HbA1c at the end of study.

Participation will last approximately 6 months. Participants enrolled in the low-dose intervention arm will receive a weekly produce delivery directly to their home in addition to the completion of 3 questionnaires and collection of the HbA1c at the end of study. The amount of produce provided in this arm will be lower per month per household size than the high dose arm.

Participation will last approximately 6 months. Participants enrolled in the Usual Care arm will complete 3 questionnaires and collection of the HbA1c at the end of study.

Outcomes

Primary Outcome Measures

Change in HbA1c between baseline and 6 months
Both intervention and control participants will have their HbA1c tested at baseline and 6 months after the baseline assessment.

Secondary Outcome Measures

Analyze the difference in difference of patient-reported food security between the intervention and control group.
Calculated by the change in self-reported food security using the US Adult Food Security Short Form (a six-item self-administered patient survey to identify food-insecure households and households with very low food security). Scores range from 0 (high or marginal food security) to 6 (very low food security).
Analyze the difference in difference of patient-reported food-related self management between the intervention and control group.
Calculated by the change in self-reported food-related self management.
Analyze the difference in difference of patient-reported diet quality between the intervention and control group.
Calculated by the change in self-reported food security using an adapted Rapid Eating Assessment of Participants Short form survey (REAP-S), which is a tool used to help care providers quickly assess a participant's diet.
Analyze the difference in difference of patient-reported nutritional security between the intervention and control group.
Calculated by change in self-reported nutrition security.

Full Information

First Posted
April 8, 2022
Last Updated
March 9, 2023
Sponsor
Kaiser Permanente
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1. Study Identification

Unique Protocol Identification Number
NCT05407376
Brief Title
Food As Medicine Study
Official Title
Produce Prescriptions at Kaiser Permanente Southern California - an Innovative 'Food as Medicine' Clinical Trial to Improve Food Insecurity and Health Among Medicaid Patients With Consistently Uncontrolled Type 2 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 11, 2021 (Actual)
Primary Completion Date
April 30, 2023 (Anticipated)
Study Completion Date
June 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kaiser Permanente

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 investigators are conducting a pre-randomized controlled trial to assess the effect of a 6 month Produce Prescription intervention for patients enrolled in Medicaid who experience consistently uncontrolled Hemoglobin A1c (HbA1c). The study is conducted at Kaiser Permanente Southern California, a large and diverse integrated health care system that serves 4.7 million members. Eligible participants are members aged 18 or older, currently enrolled in Medicaid who were diagnosed with diabetes for at least 24 months and had at least two Hba1c measurements of 7.5% or higher in the past 12 months. Patients in the intervention arm may enroll in tele nutrition counseling. The study team will recruit a total of 450. Participants, will be pre-randomized into one of three arms, 1) high dose intervention arm, a 2) low dose intervention and 3) a usual care group to achieve 150 participants enrolled in each arm. Produce is delivered weekly for participants of both intervention arms. Participants randomized to the high dose arm will receive a greater amount per month of produce versus the low dose amount (for a family of 3-4, $180 per month versus $135 respectively). Foods are provided along with recipes. The amount of food delivered is adjusted for each additional family member for up to 5 family members. The primary outcome is change in hemoglobin A1c pre-intervention and 6 months after enrollment. Secondary outcomes include, food insecurity status, dietary intake and other patient reported outcomes related to barriers to healthy eating including family conflict and cooking habits.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Intervention- High Dose
Arm Type
Active Comparator
Arm Description
Participation will last approximately 6 months. Participants enrolled in the high-dose intervention arm will receive a weekly produce delivery directly to their home in addition to the completion of 3 questionnaires and collection of the HbA1c at the end of study.
Arm Title
Intervention-Low Dose
Arm Type
Active Comparator
Arm Description
Participation will last approximately 6 months. Participants enrolled in the low-dose intervention arm will receive a weekly produce delivery directly to their home in addition to the completion of 3 questionnaires and collection of the HbA1c at the end of study. The amount of produce provided in this arm will be lower per month per household size than the high dose arm.
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
Participation will last approximately 6 months. Participants enrolled in the Usual Care arm will complete 3 questionnaires and collection of the HbA1c at the end of study.
Intervention Type
Other
Intervention Name(s)
Produce prescription (weekly produce delivery)
Intervention Description
Participants will receive weekly produce deliveries and recipes sent directly to their homes for 6 months.
Primary Outcome Measure Information:
Title
Change in HbA1c between baseline and 6 months
Description
Both intervention and control participants will have their HbA1c tested at baseline and 6 months after the baseline assessment.
Time Frame
Baseline and 6 months after baseline assessment
Secondary Outcome Measure Information:
Title
Analyze the difference in difference of patient-reported food security between the intervention and control group.
Description
Calculated by the change in self-reported food security using the US Adult Food Security Short Form (a six-item self-administered patient survey to identify food-insecure households and households with very low food security). Scores range from 0 (high or marginal food security) to 6 (very low food security).
Time Frame
Survey completed at Baseline, 3 months and 6 months
Title
Analyze the difference in difference of patient-reported food-related self management between the intervention and control group.
Description
Calculated by the change in self-reported food-related self management.
Time Frame
Survey completed at Baseline, 3 months and 6 months
Title
Analyze the difference in difference of patient-reported diet quality between the intervention and control group.
Description
Calculated by the change in self-reported food security using an adapted Rapid Eating Assessment of Participants Short form survey (REAP-S), which is a tool used to help care providers quickly assess a participant's diet.
Time Frame
Survey completed at Baseline, 3 months and 6 months
Title
Analyze the difference in difference of patient-reported nutritional security between the intervention and control group.
Description
Calculated by change in self-reported nutrition security.
Time Frame
Survey completed at Baseline, 3 months and 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 years of age or older Diagnosed with Type 2 Diabetes for at least 24 months Diagnosed with Type 2 Diabetes and have at least two HbA1cs of 7.5% or higher in 12 months prior to recruitment Have MediCaid insurance at the time of their last hba1c test Will be able to provide informed consent Will be able to consent to research activities, including receiving a weekly produce box Will be able to receive and prepare delivered foods Exclusion Criteria: Pregnant women Living in a board and care where your meals are provided for you Unable to provide informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claudia L Nau, PhD
Organizational Affiliation
Kaiser Permanente
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kaiser Permanente Southern California
City
Pasadena
State/Province
California
ZIP/Postal Code
91101
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Food As Medicine Study

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