RECRUITING

Advancing Biopsychosocial Care Training Initiative

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 compare two training approaches for US Preventive Services Task Force recommended obesity care in Federally Qualified Health Centers (FQHC) across four aims. Aim 1 compares patient-level effectiveness \[i.e., patient relative weight change and the proportion of patients who achieve clinically significant weight loss\]. Aim 2 compares reach (patient treatment utilization). Aim 3 compares primary care provider (PCP) referrals to USPSTF-recommended care at 12 (adoption) and 24 months (maintenance) and short- and long-term changes in provider obesity care competencies . Aim 4 compares implementation and service costs.

Official Title

Increasing Access to USPSTF-Recommended Obesity Care for Youth and Adults Who Are Recipients of Medicaid: Evaluation of a Comprehensive Multidisciplinary Obesity Care Training Program in FQHCs

Quick Facts

Study Start:2025-07-09
Study Completion:2029-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07049861

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:5 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  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

Aubrie Hampp, MSc
CONTACT
314-662-2005
ahampp@wustl.edu
Corinne McMahon, MS, RDN, LD
CONTACT
cnmcmahon@wustl.edu

Principal Investigator

Denise Wilfley, Ph.D.
PRINCIPAL_INVESTIGATOR
Washington University School of Medicine

Study Locations (Sites)

University of Missouri-Columbia
Columbia, Missouri, 65211
United States
Children's Mercy Hospital Kansas City
Kansas City, Missouri, 64108
United States
University of Missouri, Kansas City
Kansas City, Missouri, 64108
United States
Washington University School of Medicine
Saint Louis, Missouri, 63110
United States

Collaborators and Investigators

Sponsor: Washington University School of Medicine

  • Denise Wilfley, Ph.D., 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 Date2025-07-09
Study Completion Date2029-07-31

Study Record Updates

Study Start Date2025-07-09
Study Completion Date2029-07-31

Terms related to this study

Keywords Provided by Researchers

  • Training
  • Implementation
  • Intensive Behavioral Treatment
  • Family-based Behavioral Treatment
  • Obesity
  • Obesity Care

Additional Relevant MeSH Terms

  • Weight Management
  • Obesity Prevention
  • Obesity and Obesity-related Medical Conditions
  • Obesity and Overweight
  • Obesity