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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02947477
Other study ID # RAPFUNDEKMAN
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2016
Est. completion date December 17, 2017

Study information

Verified date January 2020
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

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.


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).


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date December 17, 2017
Est. primary completion date December 17, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria:

- Currently in Residency or Fellowship at UCSF

Exclusion Criteria:

- Not having an Iphone

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
EmoTrak
Ecological Momentary Assessment of Emotion through Iphone App

Locations

Country Name City State
United States University of California San Francisco California

Sponsors (1)

Lead Sponsor Collaborator
University of California, San Francisco

Country where clinical trial is conducted

United States, 

References & Publications (1)

Riess H, Kelley JM, Bailey RW, Dunn EJ, Phillips M. Empathy training for resident physicians: a randomized controlled trial of a neuroscience-informed curriculum. J Gen Intern Med. 2012 Oct;27(10):1280-6. Epub 2012 May 2. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Exploratory Analysis of Reduction in Pre and Post Reported Emotional Exhaustion on the MBI Exploratory analysis of pre and post reduction of participants using EmoTrak versus wait list control on Emotional Exhaustion subscale of Burnout. 30 days
Other Exploratory Analysis of Reduction in Pre and Post Reported Stress on PSS and MBI Exploratory analysis of pre and post improvements of participants using EmoTrak versus wait list control on Perceived Stress. 30 days
Other Exploratory Analysis of Increase in Pre and Post Reported Resilience on the CDRisc Exploratory analysis of pre and post improvements of participants using EmoTrak versus wait list control on a measure of resilience to dealing with stress. 30 days
Primary Retention of Participants Iphone App for Residents Quantify amount of drop out through out the 14 day study and how many reports are responded two daily 14 days
Primary Acceptability of Iphone App for Residents Online Evaluation and Mini Interviews Evaluate online questions and qualitative mini interviews about the usability of the app 30 days
Secondary Real Time Assessment Comparison to Standardized Measures Compare Pre, Post and Midway Assessments of Stress, Burnout and Emotion Awareness with daily, longitudinal measures to explore relationships between these sources of data. 35 days
Secondary Ecological Assessment of Emotions Compared to Standardized Emotion Awareness Measures, PANAS Comparing the daily reports of emotions in comparison to the PANAS scale of last week of experienced emotions 14 days
Secondary Ecological Assessment of Stress Compared to Standardized Perceived Stress and Emotional Exhaustion from the Maslach Burnout Inventory Comparing the daily reports of stress s in comparison to the week of stress as measured by PSS and MBI. 14 days
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