Rural Alliance for Diabetes Prevention (RAD)

University of Kansas

Status: Enrolling

Conditions: PreDiabetes

Treatments: Behavioral: Zoom Group Video (GV); Behavioral: Self Directed (SD)

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT06252038

STUDY00150103

R01DK132362 (U.S. NIH Grant/Contract)

Details and patient eligibility

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.

Full description

This 12 mo. Type II hybrid effectiveness-implementation trial will compare effectiveness (weight loss, physical activity, HbA1c) of Cooperative Extension delivering the Diabetes Prevention Program (DPP) by group video using Zoom® (GV) vs. a self-directed (SD) control. Active vs. passive participant recruitment strategies will be compared on recruitment outcomes including time to full enrollment, participant yield, and retention rates. Ten Cooperative Extension local units/districts serving rural Kansas counties will be allocated to either active or passive recruitment. Each of the sites will recruit adults with prediabetes living in the county served by Kansas State Research and Extension site and will be randomized to one of the 2 intervention arms. A centralized team of Cooperative Extension Agents who complete NDPP lifestyle coach training will serve as interventionists for both the GV and SD arms. Primary (weight) and secondary outcomes (HbA1c, the proportion of participants meeting weight loss (≥ 5%) and physical activity goals (≥150 min./wk.) will be assessed at baseline, 6 and 12 mos. Findings will inform best practices in the delivery of the DPP through Cooperative Extension in rural communities that could reach this high risk population.

Enrollment: 160 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age 18 years or older
• BMI ≥25 kg/m2, ≥23 kg/m2 if Asian
• Blood test results in the pre diabetic range within the last year (HbA1C = 5.7%-6.4% or fasting plasma glucose= 100-125 mg/dl or 2-hr. plasma glucose following a 75-gm glucose load = 140-199 mg/dL) or have previous diagnosis of gestational diabetes or a positive screening for pre diabetes based on CDC pre diabetes risk test
• Willing to travel to KSRE site for orientation and outcome testing
• Available to attend pre-specified meeting time of GV for their respective KSRE location
• Medically stable as deemed by primary care provider consent
• English speaking

Exclusion criteria

• Previous diagnosis of Type I or II diabetes
• Taking FDA-approved weight loss medications
• Primary care provider stating that patient should not participate
• Self-report as currently pregnant or within 6 weeks of having given birth (or planning to become pregnant in the next 12 months)
• Unable to engage in physical activity

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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160 participants in 2 patient groups

Group Video Diabetes Prevention Program

Experimental group

Description:

Participants randomized to the group video DPP for 12-months.

Treatment:

Behavioral: Zoom Group Video (GV)

Self Directed Diabetes Prevention Program

Active Comparator group

Description:

Participants randomized to the self directed DPP for 12-months.

Treatment:

Behavioral: Self Directed (SD)