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Kaiser Permanente Evaluating Nutritional Interventions in Food-Insecure High-Risk Adults Study (KP ENRICH)

Primary Purpose

Diabetes Mellitus, Type 2

Status
Not yet recruiting
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Financial support for healthy foods and free home delivery
Free home delivery
Sponsored by
Kaiser Permanente
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

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

Eligibility Criteria

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

Inclusion Criteria: Adults aged ≥18 years old at enrollment Active membership in Kaiser Permanente with Medi-Cal insurance and no additional private or commercial insurance Diagnosis of Type II diabetes mellitus (not including Type I diabetes mellitus or gestational diabetes mellitus) At least 2 outpatient glycosylated hemoglobin measures ≥7.5% in the prior 18 months Current access to the internet via computer or mobile device No interpreter needed Exclusion Criteria: Advanced or end-stage kidney disease (estimated glomerular filtration rate ≤15 ml/min/1.73m^2 or receiving outpatient dialysis or having a prior kidney transplant) Known pregnancy at time of identification

Sites / Locations

  • Kaiser Permanente Southern California Department of Research & Evaluation

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Financial Support and Free Delivery

Free Delivery

Arm Description

The intervention group will receive monthly financial support for healthy food items along with free home delivery through the Instacart platform.

The control group will receive only free home delivery through the Instacart platform.

Outcomes

Primary Outcome Measures

6-month change in glycosylated hemoglobin level
Baseline glycosylated hemoglobin will be ascertained using routine laboratory tests in the electronic health record prior to enrollment. Participants will complete glycosylated hemoglobin testing 6 months after enrollment.

Secondary Outcome Measures

12-month change in glycosylated hemoglobin level
Glycosylated hemoglobin will be ascertained using routine laboratory tests in the electronic health record at 12 months after enrollment.
Percentage of participants with glycosylated hemoglobin <7.5%
Baseline glycosylated hemoglobin will be ascertained using routine laboratory tests in the electronic health record prior to enrollment. Participants will complete glycosylated hemoglobin tests 6 months after enrollment. 12-month glycosylated hemoglobin level will be ascertained using routine laboratory tests in the electronic health record.
All-cause hospitalizations or emergency department visits
Occurrence of hospitalization or emergency department visit for any reason within 12 months after enrollment.
Change in self-reported level of food security
Participants will answer 10 questions about their food security using the USDA adult food security module. Affirmative responses to questions will be assigned 1 point in the food security scale (out of 10). Participants will be classified as being food secure (0-2 points) or food insecure (3-10 points).
Change in self-reported level of nutrition security
Participants will be asked about their level of difficulty in accessing healthy food on a 5-point Likert scale. Participants will also be asked 13 questions on reasons for not eating healthy food, with each question scored from 0-2 (Never, Sometimes, Often true). Lower scores indicate higher nutrition security.
Change in self-reported dietary habits
Participants will be asked 8 questions to examine their consumption of fast food, fruits, vegetables, legumes, nuts, dairy, seafood, sweets, and sugar-sweetened beverages over the past month.
Change in self-reported diabetes-related quality of life
Participants will answer 13 questions about their diabetes-related quality of life, each on a 5-point Likert scale. Scores range from 13-65, with higher scores indicating lower diabetes-related quality of life.
Change in self-reported readiness to change
Participants will be asked about their readiness to change their dietary habits to manage their diabetes on a 5-point Likert scale.

Full Information

First Posted
September 12, 2023
Last Updated
September 25, 2023
Sponsor
Kaiser Permanente
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1. Study Identification

Unique Protocol Identification Number
NCT06061861
Brief Title
Kaiser Permanente Evaluating Nutritional Interventions in Food-Insecure High-Risk Adults Study
Acronym
KP ENRICH
Official Title
Kaiser Permanente Evaluating Nutritional Interventions in Food-Insecure High-Risk Adults (KP ENRICH) Study
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 2023 (Anticipated)
Primary Completion Date
June 2025 (Anticipated)
Study Completion Date
December 2025 (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 goal of this randomized controlled trial is to compare the effect of receiving 6 months of monetary support for healthy food through a food delivery platform on change in glycosylated hemoglobin (HbA1c) levels among adults with type 2 diabetes mellitus with glycemic control that is above target level. The main study aims are to: To evaluate whether providing monthly financial support for home-delivered healthy food vs. only free food delivery through the Instacart platform reduces glycosylated hemoglobin levels within 6 months among Medi-Cal-insured Kaiser Permanente adult members with diabetes mellitus and suboptimal glycemic control. To evaluate whether providing monthly financial support for home-delivered healthy food vs. only free food delivery through the Instacart platform reduces medical resource utilization within 6 months among Medi-Cal-insured Kaiser Permanente adult members with diabetes mellitus and suboptimal glycemic control.
Detailed Description
Eligible Kaiser Permanente adult members will be randomized to one of two groups: Intervention arm, in which subjects will receive 6 months of monetary support (with up to 4 free home deliveries and no service fees) through the Instacart platform to select and receive healthy foods (e.g., vegetables and fruit). Control arm, in which subjects will receive 6 months of free home deliveries and no service fees for up to 4 deliveries each month through the Instacart platform. Glycosylated hemoglobin level will be assessed at baseline and at 6 months after enrollment. Medical resource utilization will be evaluated at 3 months, 6 months, and 12 months after enrollment. Patient-reported outcomes (i.e., diabetes quality of life, nutrition security, dietary habits, social needs, and food security) will also be assessed at baseline, 6 months, and 12 months after enrollment.

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
Other
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Financial Support and Free Delivery
Arm Type
Experimental
Arm Description
The intervention group will receive monthly financial support for healthy food items along with free home delivery through the Instacart platform.
Arm Title
Free Delivery
Arm Type
Experimental
Arm Description
The control group will receive only free home delivery through the Instacart platform.
Intervention Type
Other
Intervention Name(s)
Financial support for healthy foods and free home delivery
Intervention Description
Participants will receive monetary support to spend on healthy food items (e.g., vegetables and fruit) through the Instacart platform for a duration of 6 months and have home delivery and service fees waived for 4 orders per month through the Instacart platform for a duration of 6 months.
Intervention Type
Other
Intervention Name(s)
Free home delivery
Intervention Description
Participants will have home delivery and service fees waived for 4 orders per month through the Instacart platform for a duration of 6 months.
Primary Outcome Measure Information:
Title
6-month change in glycosylated hemoglobin level
Description
Baseline glycosylated hemoglobin will be ascertained using routine laboratory tests in the electronic health record prior to enrollment. Participants will complete glycosylated hemoglobin testing 6 months after enrollment.
Time Frame
6 months after enrollment
Secondary Outcome Measure Information:
Title
12-month change in glycosylated hemoglobin level
Description
Glycosylated hemoglobin will be ascertained using routine laboratory tests in the electronic health record at 12 months after enrollment.
Time Frame
12 months after enrollment
Title
Percentage of participants with glycosylated hemoglobin <7.5%
Description
Baseline glycosylated hemoglobin will be ascertained using routine laboratory tests in the electronic health record prior to enrollment. Participants will complete glycosylated hemoglobin tests 6 months after enrollment. 12-month glycosylated hemoglobin level will be ascertained using routine laboratory tests in the electronic health record.
Time Frame
6- and 12-months after enrollment
Title
All-cause hospitalizations or emergency department visits
Description
Occurrence of hospitalization or emergency department visit for any reason within 12 months after enrollment.
Time Frame
3-, 6-, and 12-months after enrollment
Title
Change in self-reported level of food security
Description
Participants will answer 10 questions about their food security using the USDA adult food security module. Affirmative responses to questions will be assigned 1 point in the food security scale (out of 10). Participants will be classified as being food secure (0-2 points) or food insecure (3-10 points).
Time Frame
6- and 12-months after enrollment
Title
Change in self-reported level of nutrition security
Description
Participants will be asked about their level of difficulty in accessing healthy food on a 5-point Likert scale. Participants will also be asked 13 questions on reasons for not eating healthy food, with each question scored from 0-2 (Never, Sometimes, Often true). Lower scores indicate higher nutrition security.
Time Frame
6- and 12-months after enrollment
Title
Change in self-reported dietary habits
Description
Participants will be asked 8 questions to examine their consumption of fast food, fruits, vegetables, legumes, nuts, dairy, seafood, sweets, and sugar-sweetened beverages over the past month.
Time Frame
6- and 12-months after enrollment
Title
Change in self-reported diabetes-related quality of life
Description
Participants will answer 13 questions about their diabetes-related quality of life, each on a 5-point Likert scale. Scores range from 13-65, with higher scores indicating lower diabetes-related quality of life.
Time Frame
6- and 12-months after enrollment
Title
Change in self-reported readiness to change
Description
Participants will be asked about their readiness to change their dietary habits to manage their diabetes on a 5-point Likert scale.
Time Frame
6- and 12-months after enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults aged ≥18 years old at enrollment Active membership in Kaiser Permanente with Medi-Cal insurance and no additional private or commercial insurance Diagnosis of Type II diabetes mellitus (not including Type I diabetes mellitus or gestational diabetes mellitus) At least 2 outpatient glycosylated hemoglobin measures ≥7.5% in the prior 18 months Current access to the internet via computer or mobile device No interpreter needed Exclusion Criteria: Advanced or end-stage kidney disease (estimated glomerular filtration rate ≤15 ml/min/1.73m^2 or receiving outpatient dialysis or having a prior kidney transplant) Known pregnancy at time of identification
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Thida C Tan, MPH
Phone
510-891-5982
Email
thida.x.tan@kp.org
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 Department of Research & Evaluation
City
Pasadena
State/Province
California
ZIP/Postal Code
91101
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Claudia Nau, PhD
Phone
626-564-5760
Email
claudia.l.nau@kp.org

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Kaiser Permanente Evaluating Nutritional Interventions in Food-Insecure High-Risk Adults Study

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