- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05019274
Culinary Medicine vs. Nutrition Education in Diabetes
March 4, 2024 updated by: Michael Edward Bowen, University of Texas Southwestern Medical Center
The Impact of Culinary Medicine vs. Nutrition Education on Diabetes Outcomes: A Randomized Trial
This pragmatic trial compares the effectiveness of virtual culinary medicine classes vs. standard of care medical nutrition visits to improve glycemic control in patients with uncontrolled type 2 diabetes .
Culinary medicine teaches healthy eating principles through a combination of experiential cooking classes and focused didactic sessions.
The primary study outcome is glycemic improvement (A1c).
Qualitative evaluation will assess participant experience, impact, and durability of behavior changes related to nutrition.
A short term cost analysis will be conducted to inform program costs and cost effectiveness.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
A total of 130 participants with uncontrolled type 2 diabetes will be recruited from a safety-net health system that provides comprehensive care for the uninsured and underinsured residents of Dallas County, Texas.
Eligible participants will be actively engaged in primary care and recruited from clinical practice.
Participants will be randomized to two arms: Culinary Medicine and standard of care medical nutrition therapy (MNT).
Certified culinary medicine instructors will deliver a series of 6 monthly Culinary Medicine classes virtually with participants cooking in their own homes.
A series of 6 standard of care medical nutrition sessions will be delivered by the health system using a combination of individual and group sessions both in person and virtually.
All participants will be enrolled in a 12 month food assistance program in partnership with community based partners to provide access to healthy foods.
Classes will be delivered over 6 months, and participants will be followed for an additional 6 months to assess the durability of glycemic response and behavior changes.
A cost analysis will examine the system cost to deliver the intervention and the short term cost effectiveness examining the cost per participant achieving a clinically meaningful reduction in A1c.
Study Type
Interventional
Enrollment (Actual)
120
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Texas
-
Dallas, Texas, United States, 75206
- Parkland Health and Hospital System
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- No nutrition visit in the past 12 months.
- Hemoglobin A1C ≥ 7.5% within the past six months.
- Diagnosed with established Type 2 Diabetes > 12 months
- Receiving primary care at Hatcher Station Health Center and an assigned primary care provider within the past 18 months.
- Completion of at least 2 of the 4 Health Living with Diabetes (HLWD) virtual and/or in-person sessions.
Exclusion Criteria:
- Patients who cannot hear virtual and/or in-person instruction
- Patients who cannot read or speak English or Spanish
- Patients who are unable to understand study information
- Patients younger than 18 years of age
- Patients who are unable to communicate with voice (for participation in phone surveys, focus groups and semi-structured interviews)
- Patients without access to a smart phone or other device with internet and/or data capability to participate in virtual classes
- We will exclude patients with chronic kidney disease (CKD) stage 4 or 5 (eGFR < 30 or on dialysis) because their renal function may require additional nutritional counseling and dietary modifications beyond the scope of the proposed culinary medicine and nutrition sessions delivered in this study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Culinary Medicine
Series of 6 virtual group Culinary Medicine sessions delivered monthly for 6 months
|
Participants randomized to the Culinary Medicine intervention will complete a series of 6 virtual culinary medicine cooking classes (1 class per month for 6 months).
Virtual sessions will be delivered via Zoom using a combination of large group instruction and small group break-out sessions in which participants prepare a recipe in their home kitchen with the virtual assistance from trained group facilitators.
After preparing the dish, participants will enjoy the dish they prepared and report-back to the large group about their dish and experience.
Classes will be conducted in English and Spanish with language-concordant instructors and facilitators.
|
|
Active Comparator: Nutrition Education
Series of 6 standard of care nutrition visits delivered by clinic dieticians.
These are a mix of individual and group sessions.
|
Participants randomized to standard of care nutrition visits will complete a series of 6 nutrition visits (1 session per month for 6 months) led by bilingual (English/Spanish) dieticians.
Sessions will consist of a mix of individual and small group sessions per standard of care in the clinic.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hemoglobin A1c
Time Frame: 3, 6, and 12 months
|
A1c will be measured at baseline, 3, 6 and 12 months.
Change in A1c will be assessed at 6 months (end of active intervention) and also at 12 months (i.e. 6 months after completion of active intervention) to assess the durability of the intervention on glycemic control.
Pre-specified subgroup analyses will also examine A1c outcomes by: 1) prior participation in diabetes education and nutrition education.
Stratified analyses by number of sessions attended will also be conducted.
|
3, 6, and 12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in weight
Time Frame: 3, 6, and 12 months
|
3, 6, and 12 months
|
|
|
Change in BMI
Time Frame: baseline, 6 and 12 months
|
baseline, 6 and 12 months
|
|
|
Change in blood pressure
Time Frame: baseline, 6, and 12 months
|
baseline, 6, and 12 months
|
|
|
Food security score
Time Frame: baseline, 6 months and 12 months
|
U.S. Household Food Security Survey Module: Six-Item Short Form.
The score ranges from 0 to 6 with 0 indicating high food security and 6 indicating very low food security.
|
baseline, 6 months and 12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Michael E Bowen, MD, UT Southwestern Medical Center in Dallas
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 9, 2021
Primary Completion (Actual)
December 31, 2023
Study Completion (Actual)
December 31, 2023
Study Registration Dates
First Submitted
July 30, 2021
First Submitted That Met QC Criteria
August 23, 2021
First Posted (Actual)
August 24, 2021
Study Record Updates
Last Update Posted (Estimated)
March 6, 2024
Last Update Submitted That Met QC Criteria
March 4, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- STU-2020-1244
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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