Home › Cardiovascular Disease › NCT06397729
Evaluation of a Novel Technology to Support Tailored Health Behavior Counseling in Rural Primary Care Clinics
Who can join
Ages 18 to 64 · All sexes
Full eligibility criteria
Patient Inclusion Criteria: * Aged 18-64 years at baseline * At risk for poor CVH (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) Provider Inclusion Criteria: • All providers and clinic staff (physicians, nurses, community health workers, clinic staff, clinic research associates) in the Missouri Highlands Healthcare Clinics are eligible to participate.
About the study
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.
What is being tested
- Wait-List Control (behavioral)
- PREVENT Tool (behavioral)
Sponsor: Washington University School of Medicine · Participants: 100 · Started: Nov 1, 2024
Contact the study team
- Maura Kepper, PhD · Phone: 314-935-0142
Official record on ClinicalTrials.gov — NCT06397729
Locations in the U.S.
| Missouri | Washington University in St. Louis, St Louis |
Conditions
From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.