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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03398460
Other study ID # 17-01695
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2018
Est. completion date August 20, 2018

Study information

Verified date June 2020
Source NYU Langone Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Description:

This study will evaluate:

1. 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.

2. 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.

3. Determine whether the introduction of a bereavement card will improve symptoms of burnout as gauged by the abbreviated maslach burnout inventory

4. Staff perceptions and response to the introduction of a bereavement


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date August 20, 2018
Est. primary completion date August 20, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Health care providers who work in the Bellevue Hospital Medical ICU

Exclusion Criteria:

- NA

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Survey
Burnout rates before and after the introduction of a bereavement card Burnout rates before and after an ICU rotation for physicians

Locations

Country Name City State
United States New York University School of Medicine New York New York

Sponsors (1)

Lead Sponsor Collaborator
NYU Langone Health

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Burnout rate before introduction of bereavement card Measured by "Staff Response Questionnaire" 1 Year
Primary Burnout rate after introduction after introduction of bereavement card Measured by "Staff Response Questionnaire" 1 Year
Primary Burnout rates before ICU rotation for physicians Measured by "Staff Response Questionnaire" 1 Year
Primary Burnout rates after an ICU rotation for physicians Measured by "Staff Response Questionnaire" 1 Year
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