Burn-out Among Chinese Anaesthesiologist After COVID-19 Pandemic Peak and Its Protective Factor: a National Survey

June 15, 2022 updated by: Huang YuGuang

Burn-out Among Chinese Anaesthesiologist After COVID-19 Pandemic Peak and Its Protective Factor: a National Survey

The investigators proposed a national representative survey to collect data of socio-demographic characteristics, level of exposure to COVID-19, depression,anxiety, ptsd, burnout and resilience of working anaesthesiologists across mainland China for the following purpose

  1. Explore the current burn-out rate of Chinese anaesthesiologists and compared it with data acquired in 2015;
  2. Explore the perceived covid-19 exposure of COVID-19 among Chinese anaesthesiologist.
  3. Explore rate of burnout, anxiety, depression, PTSD symptoms experienced by the participants
  4. Explore the protective psychosocial characteristics of burnout. (resilience)
  5. See whether covid-19 exposure contribute to higher burn out rate.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

6631

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

      • Peking, China
        • Peking Union Medical College 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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

working anaesthesiologist in mainland China

Description

Inclusion Criteria:

working anaesthesiologist in mainland China

Exclusion Criteria:

-

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

  • Observational Models: Other
  • Time Perspectives: Cross-Sectional

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Burnout
Time Frame: data will be retrieved and recored 1 week after survey distribution
Burnout level will be measured by Maslach Burnout Inventory-Human Service Survey
data will be retrieved and recored 1 week after survey distribution

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Post-Traumatic Stress Disorder
Time Frame: data will be retrieved and recored 1 week after survey distribution
The Impact of Events Scale-Revised (IES-R) is a self-reporting tool widely used in the field of psychological impact and has been proven to be suitable for the Chinese population
data will be retrieved and recored 1 week after survey distribution
Resilience
Time Frame: data will be retrieved and recored 1 week after survey distribution
10-item Connor-Davidson Resilience Scale (CD-RISC-10) was used to assess resilience.
data will be retrieved and recored 1 week after survey distribution
Depressive symptoms
Time Frame: data will be retrieved and recored 1 week after survey distribution
The Patient Health Questionnaire-9 (PHQ-9) was included to assess depressive symptoms.
data will be retrieved and recored 1 week after survey distribution
Anxiety
Time Frame: data will be retrieved and recored 1 week after survey distribution
Anxiety level will be evaluated by GAD-7 Anxiety Scale
data will be retrieved and recored 1 week after survey distribution

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)

August 1, 2021

Primary Completion (Actual)

March 1, 2022

Study Completion (Actual)

March 24, 2022

Study Registration Dates

First Submitted

July 2, 2021

First Submitted That Met QC Criteria

July 16, 2021

First Posted (Actual)

July 20, 2021

Study Record Updates

Last Update Posted (Actual)

June 21, 2022

Last Update Submitted That Met QC Criteria

June 15, 2022

Last Verified

June 1, 2022

More Information

Terms related to this study

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.

Clinical Trials on Burnout

Clinical Trials on resilience and institutional support

3
Subscribe