Actively Recruiting
Rural Alliance for Diabetes Prevention
Led by University of Kansas Medical Center · Updated on 2026-02-27
160
Participants Needed
1
Research Sites
192 weeks
Total Duration
On this page
Sponsors
U
University of Kansas Medical Center
Lead Sponsor
N
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this randomized controlled trial is to compare the effectiveness of Cooperative Extension implementing two delivery methods (group video vs. self-directed) and participant recruitment strategies of the National Diabetes Prevention Program (NDPP) to adults in rural communities. Exploratory assessments of implementation facilitators and barriers will be completed to determine strategies that may impact intervention effectiveness and that may support or impede the implementation, dissemination, and effectiveness of Cooperative Extension to deliver the NDPP to prediabetic adults in rural areas.
CONDITIONS
Official Title
Rural Alliance for Diabetes Prevention
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- BMI 65 kg/m2, 63 kg/m2 if Asian
- Blood test results in the prediabetic range within the last year (HbA1C 5.7%-6.4%, fasting plasma glucose 100-125 mg/dl, or 2-hour plasma glucose 140-199 mg/dL) or previous diagnosis of gestational diabetes or positive prediabetes screening
- Willing to travel to Kansas State Research and Extension site for orientation and outcome testing
- Available to attend scheduled group video meeting times for their location
- Medically stable as approved by primary care provider
- English speaking
You will not qualify if you...
- Previous diagnosis of Type I or II diabetes
- Taking FDA-approved weight loss medications
- Primary care provider advises against participation
- Currently pregnant, within 6 weeks postpartum, or planning pregnancy within 12 months
- Unable to engage in physical activity
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University of Kansas Medical Center
Kansas City, Kansas, United States, 66160
Actively Recruiting
Research Team
A
Annie Rice, M.S.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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