Actively Recruiting
Mountain West Prevention Research Center Core Research Project
Led by Paul Estabrooks · Updated on 2026-03-18
600
Participants Needed
1
Research Sites
260 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This hybrid type 3 effectiveness-implementation sequential multiple assignment randomized trial will assess the impact of integrating population health management (PHM) strategies-text messaging and enrollment in Building Healthy Families (BHF)-for lower-income families with a child with obesity identified through electronic health record (EHR) data. BHF promotes family healthy eating, physical activity, and lifestyle behavior strategies to manage weight. The research team will partner with clinical sites (community health clinics, pediatric clinics, rural hospitals) and Community-Based Organizations (CBOs). Clinical partners will execute data-sharing agreements enabling the research team to identify eligible children and caregivers and conduct outreach via text messaging. CBO partners will deliver BHF and provide de-identified data for program evaluation. Community Implementation Teams (CITs) will complete training, surveys, interviews, learning collaborative activities, fidelity assessments, and time tracking as part of quality improvement. The BHF Action Learning Collaborative will use quarterly sessions and Plan-Do-Study-Act cycles to address recruitment, implementation, sustainability, social determinants of health, and team coordination. The research team will record sessions, conduct direct observations of BHF delivery, and take field notes to assess fidelity and adaptations. Families will be identified through EHR records and mailed a consent and authorization cover letter, postcard, QR code, and intervention information with opt-out options. Those who do not opt out will be randomized to bidirectional text messaging with one-touch response and enrollment opportunities, with or without active outreach (telephone or text) from the local CIT. Enrolled families will complete orientation, baseline assessment, and weekly group sessions with ongoing follow-up. Attendance, body weight, goals, and self-monitoring will be recorded in a CIT data portal. Families will be randomized to receive either simple text reminders or reminders with motivational and skill-building prompts matched to session topics. CITs will also connect families to food assistance programs and local resources. Each CIT will complete two cohorts over two years. The primary outcome is reach; secondary outcomes include session attendance, changes in child BMI-z scores, changes in parent or caregiver weight, and changes in adoption, implementation, and maintenance at the community level.
CONDITIONS
Official Title
Mountain West Prevention Research Center Core Research Project
Who Can Participate
Eligibility Criteria
You may qualify if you...
Families
Parent or legal caregiver and at least one child aged 5 to 12 years
Child identified through electronic health record data from a participating clinical organization
Child has had at least one clinical encounter at the participating site within the past 12 months
Child has body mass index (BMI) at or above the 85th percentile for age and sex
Caregiver has not opted out of receiving text communication from the clinic
Valid mailing address and telephone number listed in the electronic health record
Parents and/or Caregivers
Parent or legal caregiver of an eligible child
Responsible for the child's care and able to provide consent for program participation
Children
Aged 5 to 12 years at time of identification
Meet all criteria listed above
You will not qualify if you...
Child has a medical condition or contraindication that precludes participation in moderate physical activity
Child has severe cognitive or physical impairment that would prevent participation in the intervention
Child or family is currently participating in another structured weight management or obesity treatment program
Family opts out of receiving study-related communications
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The University of Utah
Salt Lake City, Utah, United States, 84112
Actively Recruiting
Research Team
M
Madeleine L French, MS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
4
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here