600 Participants NeededMy employer runs this trial

Text Messaging for Childhood Obesity

(MW-PRCCRP Trial)

ML
Overseen ByMadeleine L French, MS
Age: Any Age
Sex: Any
Trial Phase: Academic
Sponsor: Paul Estabrooks
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

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.

Who Is on the Research Team?

PA

Paul A Estabrooks, PhD

Principal Investigator

University of Utah

Are You a Good Fit for This Trial?

Inclusion Criteria

My family includes a parent or legal caregiver and a child aged 5 to 12.
Caregiver has not opted out of receiving text communication from the clinic
Meet all criteria listed above
See 7 more

Exclusion Criteria

My family does not want to receive any study-related information.
Child has a medical condition or contraindication that precludes participation in moderate physical activity
Child or family is currently participating in another structured weight management or obesity treatment program
See 1 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Recruitment and Enrollment

Eligible families are identified through EHR data and contacted via text messaging for enrollment in the Building Healthy Families program.

Up to 3 months
Ongoing outreach via text and phone

Treatment

Families participate in weekly two-hour group sessions focusing on healthy eating, physical activity, and lifestyle behavior strategies.

12 weeks
Weekly sessions

Follow-up

Participants are monitored for changes in BMI, weight, and program engagement.

12 months
Assessments at 3, 6, and 12 months

Community Implementation and Maintenance

Community Implementation Teams continue to deliver the BHF program and assess fidelity and adaptations.

Up to 24 months

What Are the Treatments Tested in This Trial?

Interventions

  • Active outreach follow-up
  • Text Message-based recruitment

How Is the Trial Designed?

4

Treatment groups

Experimental Treatment

Group I: TM-Single-AOExperimental Treatment2 Interventions
Group II: TM-SingleExperimental Treatment1 Intervention
Group III: TM-Repeat-AOExperimental Treatment2 Interventions
Group IV: TM-RepeatExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Paul Estabrooks

Lead Sponsor