Actively Recruiting
Evaluation of a Novel Technology to Support Tailored Health Behavior Counseling in Rural Primary Care Clinics
Led by Washington University School of Medicine · Updated on 2025-06-13
100
Participants Needed
1
Research Sites
90 weeks
Total Duration
On this page
Sponsors
W
Washington University School of Medicine
Lead Sponsor
M
Missouri Highlands Health Care
Collaborating Sponsor
AI-Summary
What this Trial Is About
This project will conduct a pilot hybrid study that examines the implementation (Aims 1 \& 2) and preliminary effectiveness (Aim 3) of PREVENT, a digital health intervention, among patients with overweight/obesity (N=100) using a clinic-randomized design. The central hypothesis of the study is that PREVENT will be feasible and show improvements in health behavior counseling and the patient experience that will improve patients' motivation to change, and their CVH health behaviors and outcomes.
CONDITIONS
Official Title
Evaluation of a Novel Technology to Support Tailored Health Behavior Counseling in Rural Primary Care Clinics
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18-64 years at baseline
- Low income (household income <200% FPL)
- At risk for poor cardiovascular health (body mass index greater than or equal to 30)
- Receiving care from the Missouri Highlands Healthcare
- Ability to understand and willingness to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable)
- All providers and clinic staff in the Missouri Highlands Healthcare Clinics are eligible to participate
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Washington University in St. Louis
St Louis, Missouri, United States, 63130
Actively Recruiting
Research Team
M
Maura Kepper, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
3
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