- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04967820
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
- Explore the current burn-out rate of Chinese anaesthesiologists and compared it with data acquired in 2015;
- Explore the perceived covid-19 exposure of COVID-19 among Chinese anaesthesiologist.
- Explore rate of burnout, anxiety, depression, PTSD symptoms experienced by the participants
- Explore the protective psychosocial characteristics of burnout. (resilience)
- See whether covid-19 exposure contribute to higher burn out rate.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
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
-
-
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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.
Sponsor
Collaborators
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- CSAnationalsurveyburnout
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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