NCT lookup
Pull any trial record directly from ClinicalTrials.gov.
Sponsor: Washington University School of Medicine
Conditions: Cardiovascular Diseases, Obesity
Interventions: Wait-List Control, PREVENT Tool
Countries: United States
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.
Sex: ALL
Age: 18 Years to 64 Years
Healthy volunteers: No
Study type: INTERVENTIONAL
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.
- St Louis, Missouri, United States