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PREVENT Digital Health Tool for Cardiovascular Health in Rural Primary Care

This study is testing a new digital health tool called PREVENT. This tool is designed to help people who are overweight or obese make healthier choices about physical activity and food. It gives personalized advice and resources right in the doctor's office. The study wants to see if PREVENT helps patients and doctors feel more satisfied with health counseling. You might be able to join if you are 18-64 years old, have a BMI (Body Mass Index) of 30 or higher, and receive care from Missouri Highlands. The study is currently unclear on its status and plans to enroll about 60 people.

Study design
This study is interventional and plans to enroll 60 participants. Some participants will use the PREVENT tool, while others will receive routine care and then get access to PREVENT later.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Patient satisfaction with PREVENT will be measured at 6 months. Provider satisfaction will be measured up to 12 weeks post-study.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06063564

Adapting and Testing a Novel Digital Health Tool (PREVENT) to Improve Health Behavior Counseling and Cardiovascular Health in Rural Primary Care Clinics

Recruiting
NAAges 18–64InterventionalPrevention
Washington University School of Medicine
~60 participants
Updated 2026-07-16 on ClinicalTrials.gov
What's tested:PREVENTWait-list Control

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Patients' satisfaction of PREVENT tool: survey
Measured over 6-months
+2 more outcomes measured

Conditions

Obesity
Cardiovascular Diseases

Explore related trials

Cardiovascular DisorderObesity

Where it's being run

1 sites across 1 states
Missouri1

Who to contact

Maura M Kepper, PhD
[email protected]
3149350142
Email the study team

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Aged 18-64 years at baseline
a BMI ≥ 30
Receiving care from the Missouri Highlands.
Ability to understand and willingness to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable).

What this trial measures

  • Patients' satisfaction of PREVENT tool: survey6-months

    A survey (6-questions) will assess patient's satisfaction with the PREVENT tool. Questions are asked on a 5-point Likert scale (range: 6-30) with a higher score indicating greater satisfaction.

  • Provider's satisfaction of PREVENT tool: surveyUp to 12 weeks post-study

    A survey (31-questions) will assess provider's acceptability and satisfaction with five aspects of health information technology: content, accuracy, format, ease of use and timeliness. Questions are asked on a 5-point Likert scale (range: 31-155) with a higher score indicating greater satisfaction.

  • Fidelity of PREVENT tool implementation0-6 months

    Fidelity will be measured using direct observation of patient-provider interactions while using the PREVENT tool. A direct observation checklist will be used by the observer to determine the number of interactions with the PREVENT tool that were implemented as intended.