- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04992364
Clinical Impacts of Burnout Syndrome Among Anesthesiology Residents
July 29, 2021 updated by: Aida Rosita Tantri, Indonesia University
Relationship Between Burnout Score and Clinical Performance on Anesthesiology and Intensive Therapy Residents
This study aimed to determine the relationship between burnout levels and clinical performances of anesthesiology residents.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Fifty-five second until fourth year anesthesiology residents, who were not on any mental medication treatment, were recruited consecutively and asked to fill out questionnaires which are; the Maslach Burnout Inventory (MBI) questionnaire to assess burnout levels, Best Practice Anesthesiologist questionnaire to assess positive clinical performance, Anesthesiology Residents' Self-Reported Errors and Quality of Care questionnaire to assess negative clinical performance.
Study Type
Observational
Enrollment (Actual)
55
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
-
-
DKI Jakarta
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Jakarta, DKI Jakarta, Indonesia, 10430
- Cipto Mangunkusumo Cental National Hospital
-
-
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
25 years to 35 years (Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Anesthesiology residents who were on second until fourth year of residency
Description
Inclusion Criteria:
- second until fourth year anesthesiology residents
- not on any mental medication treatment
- willing to participate
Exclusion Criteria:
- on paid leave
- rejected to become the sample
- had their shift in 24 hours prior to this study
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Positive Clinical Performances
Subjects show positive clinical performances regarding burnout syndrome
|
Subjects were given questionnaires to assess burnout score and clinical performances
|
|
Negative Clinical Performances
Subjects show negative clinical performances regarding burnout syndrome
|
Subjects were given questionnaires to assess burnout score and clinical performances
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Positive clinical performance
Time Frame: 1 month through study completion
|
Subjects show positive clinical performance
|
1 month through study completion
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Negative clinical performance
Time Frame: 1 month through study completion
|
Subjects show negative clinical performance
|
1 month through study completion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
January 10, 2019
Primary Completion (Actual)
February 27, 2019
Study Completion (Actual)
December 30, 2019
Study Registration Dates
First Submitted
July 13, 2021
First Submitted That Met QC Criteria
July 29, 2021
First Posted (Actual)
August 5, 2021
Study Record Updates
Last Update Posted (Actual)
August 5, 2021
Last Update Submitted That Met QC Criteria
July 29, 2021
Last Verified
July 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IndonesiaUAnes107
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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