RECRUITING

Evaluation of a Novel Technology to Support Tailored Health Behavior Counseling in Rural Primary Care Clinics

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Evaluation of a Novel Technology to Support Tailored Health Behavior Counseling in Rural Primary Care Clinics

Quick Facts

Study Start:2024-11-01
Study Completion:2026-07-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06397729

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 64 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Aged 18-64 years at baseline
  2. * Low income (household income \<200% FPL)
  3. * At risk for poor CVH (body mass index greater than or equal to 30)
  4. * Receiving care from the Missouri Highlands Healthcare
  5. * Ability to understand and willingness to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable)
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Maura Kepper, PhD
CONTACT
314-935-0142
kepperm@wustl.edu

Principal Investigator

Maura Kepper, PhD
PRINCIPAL_INVESTIGATOR
Washington University School of Medicine

Study Locations (Sites)

Washington University in St. Louis
St. Louis, Missouri, 63130
United States

Collaborators and Investigators

Sponsor: Washington University School of Medicine

  • Maura Kepper, PhD, PRINCIPAL_INVESTIGATOR, Washington University School of Medicine

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-11-01
Study Completion Date2026-07-30

Study Record Updates

Study Start Date2024-11-01
Study Completion Date2026-07-30

Terms related to this study

Keywords Provided by Researchers

  • Digital health
  • Behavior Change
  • Physical Activity
  • Diet
  • Cardiovascular Disease
  • Obesity
  • Rural health

Additional Relevant MeSH Terms

  • Cardiovascular Diseases
  • Obesity