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

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
      • 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.

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

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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