- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04861272
Risk Perception Associated With Covid-19 Among Anesthetists
April 25, 2021 updated by: SALAH EL-TALLAWY, King Saud University
RISK PERCEPTION ASSOCIATED WITH COVID-19 PANDEMIC AMONG ANESTHETISTS: A Cross-Sectional Study
Since the outbreak of the COVID-19 pandemic, the anesthesiologists are involved in the riskiest interventions e.g.
airway management, endotracheal intubation, and resuscitation.
So, they are subjected to a higher risk of infection compared to many other medical specialties.
As a result, they are more subjected to psychological stresses.
This study aimed to assess the level of stress associated with the COVID-19 pandemic among anesthesiologists.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
This is a cross-sectional, hospital-based survey conducted using an online questionnaire after getting IRB approval.
The primary outcomes are to evaluate the prevalence of anxiety, depression, and post-traumatic stress disorder (PTSD) among anesthesiologists working in Saudi Arabia.
The secondary outcomes include the association of the socio-demographic and occupational characteristics with mental health in the study sample.
The survey sent to the target participants using a web-based software platform (https://www.surveymonkey.com/r/ZJ98BTJ)
though the Saudi Society of Anesthesia.
The study sample included anesthetists and their allied health care providers (nurses and technicians) involved in the management of COVID-19 patients.
Data were analyzed using SPSS version 21.
Descriptive analyses were conducted, and the ranked data for each level for symptoms of depression, anxiety, and PTSD were presented as numbers and percentages.
Multi-variable logistic regression analysis was used to explore potential influence factors on the outcomes.
P-values of less than 0.05 were considered statistically significant.
Study Type
Observational
Enrollment (Anticipated)
1000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: SALAH N. EL-TALLAWY, MD
- Phone Number: +966557931195
- Email: salaheltallawy@yahoo.com
Study Contact Backup
- Name: Maher A Titi, MSc
- Phone Number: +966568310277
- Email: mahertiti1980@gmail.com
Study Locations
-
-
-
Riyadh, Saudi Arabia, 7805
- Recruiting
- Salah N. El-Tallawy
-
Contact:
- SALAH N. EL-TALLAWY
- Phone Number: 0114692191
-
-
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
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
- Participants' demographic variables such as gender, age, years of experience, educational degree, position at the hospital, unit of work and hospital type.
- Outcome variables: The prevalence of Anxiety, Depression and Posttraumatic Stress Disorder (PTSD)
Description
Inclusion Criteria:
- The survey included anesthesia physicians, anesthesia technicians and nurses, and those involved in the management of COVID-19 infected patients in the OR, ICU, or ER.
Exclusion Criteria:
- The exclusion criteria include age < 18 or > 60 years, incomplete data, or those who were outside Saudi Arabia during the time of the COVID-19 pandemic.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
- The prevalence of Anxiety, Depression, and Posttraumatic Stress Disorder (PTSD) among anesthesiologists during COVID-19 pandemic.
Time Frame: 2 weeks
|
Online survey
|
2 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
- Comparison of the prevalence of anxiety, depression, and level of stress among different groups e.g. males # females, different occupations, single # married, young, middle-aged # geriatrics
Time Frame: 2 weeks
|
Online survey
|
2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: SALAH N. EL-TALLAWY, MD, KING SAUD UNIVERSITY, Riyadh, Saudi Arabia
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)
April 15, 2021
Primary Completion (Anticipated)
May 5, 2021
Study Completion (Anticipated)
May 15, 2021
Study Registration Dates
First Submitted
April 25, 2021
First Submitted That Met QC Criteria
April 25, 2021
First Posted (Actual)
April 27, 2021
Study Record Updates
Last Update Posted (Actual)
April 27, 2021
Last Update Submitted That Met QC Criteria
April 25, 2021
Last Verified
April 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB approval No. E-20-4975
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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