- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02947477
Emotion Tracking Study for Residents (ETSR)
January 14, 2020 updated by: University of California, San Francisco
EmoTrak, Ecological Momentary Assessment of Emotion, Stress and Satisfaction Among Residents
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.
Study Overview
Detailed 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 Type
Interventional
Enrollment (Actual)
100
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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California
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San Francisco, California, United States, 94114
- University of California
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
17 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Currently in Residency or Fellowship at UCSF
Exclusion Criteria:
- Not having an Iphone
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Treatment
The EMA intervention uses twice-a-day interactive questions for emotion tracking including type of emotion, intensity of emotion, trigger to emotion and response to emotion through an Iphone app designed for the study.
The study users receive individualized feedback about their daily reporting of emotions, sleep and stress.The study tracking is for 14 days.
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Ecological Momentary Assessment of Emotion through Iphone App
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No Intervention: Control
The control arm does nothing for 14 days and then receives the 14 day emotion tracking listed above.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Retention of Participants Iphone App for Residents
Time Frame: 14 days
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Quantify amount of drop out through out the 14 day study and how many reports are responded two daily
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14 days
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Acceptability of Iphone App for Residents Online Evaluation and Mini Interviews
Time Frame: 30 days
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Evaluate online questions and qualitative mini interviews about the usability of the app
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30 days
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Real Time Assessment Comparison to Standardized Measures
Time Frame: 35 days
|
Compare Pre, Post and Midway Assessments of Stress, Burnout and Emotion Awareness with daily, longitudinal measures to explore relationships between these sources of data.
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35 days
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Ecological Assessment of Emotions Compared to Standardized Emotion Awareness Measures, PANAS
Time Frame: 14 days
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Comparing the daily reports of emotions in comparison to the PANAS scale of last week of experienced emotions
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14 days
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Ecological Assessment of Stress Compared to Standardized Perceived Stress and Emotional Exhaustion from the Maslach Burnout Inventory
Time Frame: 14 days
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Comparing the daily reports of stress s in comparison to the week of stress as measured by PSS and MBI.
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14 days
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Exploratory Analysis of Reduction in Pre and Post Reported Emotional Exhaustion on the MBI
Time Frame: 30 days
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Exploratory analysis of pre and post reduction of participants using EmoTrak versus wait list control on Emotional Exhaustion subscale of Burnout.
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30 days
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Exploratory Analysis of Reduction in Pre and Post Reported Stress on PSS and MBI
Time Frame: 30 days
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Exploratory analysis of pre and post improvements of participants using EmoTrak versus wait list control on Perceived Stress.
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30 days
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Exploratory Analysis of Increase in Pre and Post Reported Resilience on the CDRisc
Time Frame: 30 days
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Exploratory analysis of pre and post improvements of participants using EmoTrak versus wait list control on a measure of resilience to dealing with stress.
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30 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Eve Ekman, PhD, University of California, San Francisco
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2016
Primary Completion (Actual)
December 17, 2017
Study Completion (Actual)
December 17, 2017
Study Registration Dates
First Submitted
October 24, 2016
First Submitted That Met QC Criteria
October 25, 2016
First Posted (Estimate)
October 28, 2016
Study Record Updates
Last Update Posted (Actual)
January 18, 2020
Last Update Submitted That Met QC Criteria
January 14, 2020
Last Verified
January 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- RAPFUNDEKMAN
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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