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Clinical Trial Summary

The proposed study will develop and pilot a fourteen-day assessment tailored for the high-demand schedule of residents through a smart phone intervention, EmoTrak.EmoTrak uses ecological measurement assessment (EMA), which solicits real-time user feedback at various time points across a series of days or weeks.


Clinical Trial Description

The investigators will perform a randomized controlled trial that compares residents, using EmoTrak with a wait list control group. After two weeks, the active control group becomes the treatment group. All participants will be evaluated four times from at baseline to two months. The measures to explore for any pre and post change are stress reduction on the emotional exhaustion scale of the Maslach Burnout Inventory (MBI) and improved resilience on the Perceived Stress Scale (PSS). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02947477
Study type Interventional
Source University of California, San Francisco
Contact
Status Completed
Phase N/A
Start date October 2016
Completion date December 17, 2017

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