Tests a diabetes prevention program adapted for underserved African Americans
Tests diabetes prevention program versions for African Americans with prediabetes or obesity.
Key facts
- Who runs it
- University of Missouri, Kansas City
- Where
- Kansas City, United StatesSee the 2 sites
- Trial code
- Registry title
- Social Determinants and a Diabetes Prevention Program Tailored for African Americans
- Status
- Recruiting
- Phase
- Phase 2
- People taking part
- 360 people, planned
- Started
- 20 Jul 2022
- Planned end
- 28 Feb 2026
- Type of study
- Interventional, 3 groupsOne group gets an existing treatment, for comparison.
- Treatments tested
- Culturally Tailored Diabetes Prevention Program
- Culturally Tailored DPP Enhanced with Socioeconomic Supports
- Diabetes Prevention Program
- Record updated
- 25 May 2025
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for Black or African American adults who are overweight and have prediabetes or a high risk of diabetes. It tests diabetes prevention programs.
- Age
- 18 years or older
- Sex
- All sexes can join
- Disease stage
- Overweight (BMI above 24) and prediabetes, or earlier gestational diabetes, or a high-risk result on a prediabetes risk test
- Earlier treatment
- Cannot be in a weight loss program now, and cannot have had weight loss (bariatric) surgery in the last year
Main reasons for not taking part
- Diagnosed with diabetes
- Pregnant, planning pregnancy in the next year, breastfeeding, or gave birth in the last 6 months
- Not fluent in English
- Had heart failure
- Not willing to use a fitness tracker, wi-fi scale and the internet
The registry criteria, word for word
Show all 14 criteriaShow less
Who can take part
- Black/African American
- Overweight ([BMI> 24); and
- Diagnosed with prediabetes OR pre-diagnosed with gestational diabetes OR high risk result on prediabetes risk test
Who cannot take part
- Bariatric weight loss surgery in last year
- Diagnosed with diabetes
- Currently have a medical condition that causes drastic weight loss
- Had heart failure
- Pregnant
- Not fluent in English
- Currently pregnant, planning a pregnancy in the next year, currently breastfeeding or have given birth in the last 6 months
- Currently participating in a weight loss program
- Cannot walk a 1-block distance without assistance and without stopping due to pain, tightness, or pressure in the chest
- Not willing to use a fitness tracker, wi-fi scale, and the internet
- Not available in the evening one day each week to participate in a class
Where in United States
- University HealthKansas City, United StatesContact: Betty Drees, M.D.Not yet recruiting
- University of Missouri-Kansas CityKansas City, United StatesContact: Jannette Berkley-Patton, PhDTaking people
About the trial
What the trial wants to find out
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.
The 3 groups in the trial
- StandardExisting treatment, for comparison
Standard Diabetes Prevention Program (DPP)
Treatment: Diabetes Prevention Program
- Culturally Tailored DPPTreatment being tested
DPP culturally tailored for African Americans
Treatment: Culturally Tailored Diabetes Prevention Program and Diabetes Prevention Program
- Culturally Tailored DPP Enhanced with Socioeconomic SupportsTreatment being tested
Culturally tailored DPP plus promotions for class attendance, hybrid attendance (in-person and virtual), and linkage to care services provided by a community health worker
Treatment: Culturally Tailored Diabetes Prevention Program, Culturally Tailored DPP Enhanced with Socioeconomic Supports, and Diabetes Prevention Program
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Addressing Social Determinants of Health to Improve Diabetes Prevention Program Outcomes Among Underserved African Americans (FIT4ALL Project)
- Plain-language title
- Tests a diabetes prevention program adapted for underserved African AmericansGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 12 November 2026.
- Record updated
- 25 May 2025