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NCT07479498Toboroz

Mountain West Prevention Research Center Core Research Project

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. márc. 18.

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Rövid összefoglaló (regiszter, angolul)

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.

Állapot (regiszter)
Toboroz
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
600 (tervezett)
Első benyújtás
2026. márc. 8.
Kezdés
2024. szept. 30.
Elsődleges befejezés
2029. szept. 29.
Fő szponzor
Paul Estabrooks
Betegségek
Elhízás
NCT-szám
NCT07479498

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó
  • Tervezett résztvevők: 600
  • 2024. szept. 30. és az elsődleges befejezés (2029. szept. 29.) között
  • 1 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

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Korábbi kezelés

  • Family opts out of receiving study-related communications

Más betegség

  • 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

Egyéb

  • Child or family is currently participating in another structured weight management or obesity treatment program

Kiket keres a vizsgálat

  • 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

Nem: nők és férfiak · Egészséges önkénteseket is fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (1)

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HelyszínVárosOrszágHelyszín állapota
The University of UtahSalt Lake CityEgyesült ÁllamokToboroz

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