- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03811990
Does a Phone-based Meditation Application Improve Mental Wellness in Emergency Medicine Personnel?
Emergency medicine is notorious for its high rate of burnout and mental health issues. The emergency department (ED) is a high paced work environment dealing with life and death issues. Employees in the ED work shift times that are not conducive to a natural circadian rhythm. All of these factors lead to high rates of burnout and overall dissatisfaction with their career choice. These are known downsides of a career in emergency medicine, but little effort is put into addressing this issue in everyday EDs.
Cell phones offer an easy and convenient means to participate in meditation. There are multiple evidence-based meditation apps available to cell phone users free of charge. Meditation has been shown to decrease burnout, rates of depression, and rates of anxiety. We hypothesize that weekly use of a meditation-based cell phone application will improve the mental health of emergency department employees as measured on various wellness inventories.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Keith Lambert, MD
- Phone Number: 7206294136
- Email: KLambert@asecnsion.org
Study Locations
-
-
Texas
-
Austin, Texas, United States, 78701
- Recruiting
- University of Texas Austin
-
Contact:
- Keith Lambert, MD
- Phone Number: 7206294136 720-629-4136
- Email: KLambert@asecnsion.org
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Employment in the Emergency Department (with at least 8 shifts a month at Dell Seton Medical Center or Seton Medical Center) as either an attending physician, resident physician, or nurse
- Age greater than/equal to 18 years old and younger than 75 years old
- Must own a mobile phone operating on the iOS system
Exclusion Criteria:
- Already use a phone-based meditation app on a weekly basis
- Currently undergoing psychological treatment in the form of weekly therapy or psychotropic medications
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control
|
|
Active Comparator: Intervention
|
Phone-based meditation application
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in depression score
Time Frame: 90 and 180 days
|
Beck Depression Inventory, numeric score of 0-63 with a score of 63 being the most depressed
|
90 and 180 days
|
Change in anxiety score
Time Frame: 90 and 180 days
|
Beck Anxiety Inventory, numeric score of 0-63 with a score of 63 being the most anxious
|
90 and 180 days
|
Change in stress levels
Time Frame: 90 and 180 days
|
Perceived Stress Scale, numeric score of 0-40 with a score of 40 being the most stressed
|
90 and 180 days
|
Change in burnout level
Time Frame: 90 and 180 days, numeric scale between 0 and 6 with 6 being the highest score
|
Maslach Burnout Inventory, measures level of stress on a numeric scale
|
90 and 180 days, numeric scale between 0 and 6 with 6 being the highest score
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Keith Lambert, MD, University of Texas at Austin
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2018-04-0089
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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