Develop site specific recruitment processes Develop site specific protocol for the randomized controlled trial Get IRB approval for the randomized controlled trial Identify eligible clinicians and engage them in participating in the study Recruit 200 participants over 18 months Use centralized randomization and data collection processes The Site PI will participate in regular project research meetings The Site RA will participate in regular project staff meetings All study data will be transferred to the University of Utah for analyses. Video and/or audio data will also be transferred to Mayo Clinic for analysis. 11. Data will be stored for the purposes of secondary research and publication.
|Effective start/end date||7/1/19 → 6/30/22|
- University of Utah (NO. 10048928-02//18SFRN34110489)
- American Heart Association (NO. 10048928-02//18SFRN34110489)
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