Actively Recruiting
Social Determinants and a Diabetes Prevention Program Tailored for African Americans
Led by University of Missouri, Kansas City · Updated on 2025-05-25
360
Participants Needed
2
Research Sites
188 weeks
Total Duration
On this page
Sponsors
U
University of Missouri, Kansas City
Lead Sponsor
U
University of Massachusetts, Amherst
Collaborating Sponsor
AI-Summary
What this Trial Is About
African Americans (AAs) have rates of diabetes mellitus (DM) twice that of Whites and are disproportionately affected by leading risk factors for DM - obesity and low-income. A critical strategy in the battle against DM is the Diabetes Prevention Program (DPP), an evidence-based intervention that significantly delays or prevents Type 2 diabetes through the promotion of diet change, exercise and modest weight loss. However, weight loss from the DPP among AAs is about half that of White participants, and suboptimal AA attendance is a critical contributor. The investigators propose to conduct a study that will address social determinants (SD) that challenge DPP attendance with underserved African Americans from a safety net hospital. The investigators will examine DPP attendance and weight loss with participants randomized to 3 groups: standard DPP, a culturally-tailored DPP to address acceptability, and a culturally-tailored DPP enhanced to address socioeconomic-related barriers to DPP participation. This novel study is the first to tailor the DPP to address SD cultural and socioeconomic barriers that limit DPP attendance and reduce its effectiveness on outcomes. The proposed multidimensional, SD tailored DPP has great potential to be a feasible and scalable model to reduce DM risks among urban, African Americans and ultimately reduce DM disparities.
CONDITIONS
Official Title
Social Determinants and a Diabetes Prevention Program Tailored for African Americans
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Black/African American
- Overweight with BMI greater than 24
- Diagnosed with prediabetes, gestational diabetes, or have a high risk result on a prediabetes risk test
You will not qualify if you...
- Diagnosed with diabetes
- Pregnant, planning pregnancy in next year, breastfeeding, or gave birth in past 6 months
- Not fluent in English
- Currently in a weight loss program
- Have a medical condition causing drastic weight loss
- Had bariatric weight loss surgery in the last year
- Unable to walk one block without chest pain or pressure
- History of heart failure
- Unwilling to use a fitness tracker, wifi scale, or internet
- Not available one evening per week for class participation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
University Health
Kansas City, Missouri, United States, 64108
Not Yet Recruiting
2
University of Missouri-Kansas City
Kansas City, Missouri, United States, 64108
Actively Recruiting
Research Team
C
Christopher Winders
CONTACT
C
Carole Bowe Thompson
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
3
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