Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06252038

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

University of Kansas Medical Center

Kansas City, Kansas, United States, 66160

Actively Recruiting

Loading map...

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here