Clinical Impacts of Burnout Syndrome Among Anesthesiology Residents

Burnout, Caregiver Clinical Trial

Official title:

Relationship Between Burnout Score and Clinical Performance on Anesthesiology and Intensive Therapy Residents

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04992364
• Other study ID #: IndonesiaUAnes107
• Status: Completed
• Start date: January 10, 2019
• Est. completion date: December 30, 2019

Study information

• Verified date: July 2021
• Source: Indonesia University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

This study aimed to determine the relationship between burnout levels and clinical performances of anesthesiology residents.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 55
• Est. completion date: December 30, 2019
• Est. primary completion date: February 27, 2019
• Gender: All
• Age group: 25 Years to 35 Years

Eligibility

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

Related Conditions & MeSH terms

• Burnout, Caregiver
• Burnout, Psychological

Intervention

Other:
• Burnout and Clinical performances questionnaires
Subjects were given questionnaires to assess burnout score and clinical performances

Locations

Country	Name	City	State
Indonesia	Cipto Mangunkusumo Cental National Hospital	Jakarta	DKI Jakarta

Sponsors (1)

Lead Sponsor	Collaborator
Indonesia University

Country where clinical trial is conducted

Indonesia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Positive clinical performance	Subjects show positive clinical performance	1 month through study completion
Secondary	Negative clinical performance	Subjects show negative clinical performance	1 month through study completion