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Culinary Medicine vs. Nutrition Education in Diabetes

Not Applicable
Completed
Conditions
Primary Disease: 1. Type 2 Diabetes
Interventions
Other: Culinary Medicine Intervention
Other: Standard of Care Nutrition Visits
Registration Number
NCT05019274
Lead Sponsor
University of Texas Southwestern Medical Center
Brief Summary

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.

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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
120
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 & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Culinary MedicineCulinary Medicine InterventionSeries of 6 virtual group Culinary Medicine sessions delivered monthly for 6 months
Nutrition EducationStandard of Care Nutrition VisitsSeries of 6 standard of care nutrition visits delivered by clinic dieticians. These are a mix of individual and group sessions.
Primary Outcome Measures
NameTimeMethod
Hemoglobin A1c3, 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.

Secondary Outcome Measures
NameTimeMethod
Food security scorebaseline, 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.

Change in weight3, 6, and 12 months
Change in BMIbaseline, 6 and 12 months
Change in blood pressurebaseline, 6, and 12 months

Trial Locations

Locations (1)

Parkland Health and Hospital System

🇺🇸

Dallas, Texas, United States

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