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

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

Study Contact Backup

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.

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

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.

Clinical Trials on Cross Sectional Hospital Based Study

Clinical Trials on Survey

3
Subscribe