Actively Recruiting

Phase 2
Age: 18Years +
All Genders
Healthy Volunteers
NCT05301413

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

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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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

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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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