N/A
Completed N=137
Learn, Engage, Act, Process (LEAP) for MOVE!
Source: ClinicalTrials.gov NCT02825680 ↗Enrolled (actual)
137
Serious AEs
—
Results posted
Oct 2020
Primary outcomePrimary: Rate of MOVE! Visits Per 1000 Candidate Veterans — 4.504; 4.853; 4.824; 5.061 Rate of MOVE! Visits per 1000 Candidate — p=.011
Summary
The overall goal of this project is to test whether the Learn. Engage. Act. Process (LEAP) intervention helps teams within the Veterans Health Administration's (VHA) local MOVE! group weight management programs be more in line with guidance. Forty-eight sites will be randomized to the LEAP intervention, which is a virtually delivered program that relies on the Institute for Healthcare Improvement (IHI) Model for Improvement, an online learning platform for clinician teams to share ideas and progress, an audit and feedback process, and a barrier buster tool. The LEAP intervention will be compared to active support that is provided to all VA MOVE! programs by the National Center for Health Promotion and Disease Prevention (NCP). The investigators will compare whether participation in LEAP results in engaging more Veterans in the MOVE! weight management program compared to facilities not participating in LEAP. The investigators will also collect information to understand what components of LEAP worked best and how to scale up so more teams can participate in LEAP.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Rate of MOVE! Visits Per 1000 Candidate Veterans |
4.504; 4.853; 4.824; 5.061 | .011 sig |
Eligibility Criteria
Inclusion Criteria
- Unit of randomization is facility.
- MOVE! group program in a VA Medical Center.
- MOVE! coordinators at medical centers who express interest in participating in the trial prior to the first cohort randomization.
Exclusion Criteria
- Unit of randomization is facility.
- Facilities that are not a medical center e.g., community-based outpatient clinic, Veteran service center
Data sourced from ClinicalTrials.gov (NCT02825680). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.