- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03398460
Burnout and Approach to Bereavement Initiatives in a Medical Intensive Care Unit (ICU)
June 4, 2020 updated by: NYU Langone Health
Given the stress, exhaustion and close interface with death that Intensive Care Unit (ICU) health care providers face, this study will evaluate burnout rates in intensive care unit (icu) physicians, nurses and ancillary staff.
Investigators will also study the effect on a bereavement card on these burnout rates
Study Overview
Detailed Description
This study will evaluate:
- Burnout rates among nurses and ancillary staff with the Abbreviated Maslach burnout inventory. This is a well validated tool that is used to evaluate symptoms of burnout such as denationalization, emotional exhaustion and lack of personal accomplishment.
- Burnout rates at the beginning of and at the end of the house staff's ICU rotation to gauge the effect of an ICU rotation on burnout rates amon medical trainees.
- Determine whether the introduction of a bereavement card will improve symptoms of burnout as gauged by the abbreviated maslach burnout inventory
- Staff perceptions and response to the introduction of a bereavement
Study Type
Interventional
Enrollment (Actual)
50
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
-
-
New York
-
New York, New York, United States, 10016
- New York University School of Medicine
-
-
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
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Health care providers who work in the Bellevue Hospital Medical ICU
Exclusion Criteria:
- NA
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: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Health Care Providers
Bellevue hospital Medical Intensive Care Unit; 30 Nurses and 50 physcians
|
Burnout rates before and after the introduction of a bereavement card Burnout rates before and after an ICU rotation for physicians
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Burnout rate before introduction of bereavement card
Time Frame: 1 Year
|
Measured by "Staff Response Questionnaire"
|
1 Year
|
Burnout rate after introduction after introduction of bereavement card
Time Frame: 1 Year
|
Measured by "Staff Response Questionnaire"
|
1 Year
|
Burnout rates before ICU rotation for physicians
Time Frame: 1 Year
|
Measured by "Staff Response Questionnaire"
|
1 Year
|
Burnout rates after an ICU rotation for physicians
Time Frame: 1 Year
|
Measured by "Staff Response Questionnaire"
|
1 Year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Vikramjit Mukherjee, NYU Langone Health
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 (Actual)
March 1, 2018
Primary Completion (Actual)
August 20, 2018
Study Completion (Actual)
August 20, 2018
Study Registration Dates
First Submitted
January 8, 2018
First Submitted That Met QC Criteria
January 8, 2018
First Posted (Actual)
January 12, 2018
Study Record Updates
Last Update Posted (Actual)
June 5, 2020
Last Update Submitted That Met QC Criteria
June 4, 2020
Last Verified
June 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 17-01695
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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