The Impact of Gender Stereotypes on Fiberoptic Intubation Performance

March 18, 2024 updated by: Murat Tümer, MD, V.K.V. American Hospital, Istanbul

The Impact of Gender Stereotypes on Fiberoptic Intubation Performance: A Randomized Controlled Simulation Study

Gender bias and stereotypes have been recognized as pervasive factors influencing various aspects of society, including professional settings. Within the realm of medical practice, understanding the potential impacts of such biases on performance is of paramount importance. Anesthesiology, a field that demands technical precision, teamwork, and rapid decision-making, is not immune to the potential effects of gender stereotypes on performance outcomes. This study aims to explore the potential influence of gender stereotype manipulation and stereotype threat on the fiber-optic intubation (FOE) performance of female anesthesiology residents.

Stereotype threat refers to the apprehension individuals experience when their actions or abilities are evaluated within the context of negative stereotypes associated with their social group. Such threat has been shown to adversely affect cognitive and motor performance in various domains. In medical education, where skills are honed through training, understanding the role of stereotype threat is crucial to fostering equitable learning environments and ensuring patient safety.

Study Overview

Study Type

Interventional

Enrollment (Actual)

51

Phase

  • Not Applicable

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

      • İstanbul, Turkey
        • VKV Amerikan Hastanesi

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

1.Residents in the Department of Anesthesiology and Reanimation at Hacettepe University Faculty of Medicine, who have completed their initial year of residency and have prior experience in FOE.

Exclusion Criteria:

  1. Not meeting the above criteria
  2. Not willing to participate in the study

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

  • Primary Purpose: Diagnostic
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Female anesthesiologists in the experimental group
Stereotype threat manipulation will be performed on the female anesthesiologist in the experimental group just before they are taken into the testing room.
Stereotype threat is the thought that a person will be negatively evaluated and judged regarding a negative stereotype that belongs to the group to which he/ she belongs. Stereotype threat manipulation will be performed on the male and female participants in the experimental group just before they are taken into the testing room. For manipulation, the following sentences will be said to the participants in the experimental group: "We aim to compare fiberoptic intubation performance between male and female anesthesiologists. Additionally, we are investigating whether the high inclination of males towards computer games has any impact on their fiberoptic intubation success." The other participants (Control Group) will not be given any prior information.
No Intervention: Female anesthesiologists in the control group
The female anesthesiologists in the control group will not be given any prior information.
Experimental: Male anesthesiologist in the experimental group
Stereotype threat manipulation will be performed on the male anesthesiologist in the experimental group just before they are taken into the testing room.
Stereotype threat is the thought that a person will be negatively evaluated and judged regarding a negative stereotype that belongs to the group to which he/ she belongs. Stereotype threat manipulation will be performed on the male and female participants in the experimental group just before they are taken into the testing room. For manipulation, the following sentences will be said to the participants in the experimental group: "We aim to compare fiberoptic intubation performance between male and female anesthesiologists. Additionally, we are investigating whether the high inclination of males towards computer games has any impact on their fiberoptic intubation success." The other participants (Control Group) will not be given any prior information.
No Intervention: Male anesthesiologist in the control group
The male anesthesiologists in the control group will not be given any prior information.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Fİberoptic Intubation (FOE) Performance
Time Frame: During FOE simulation
Change in FOE scores in the experimental group compared to the control group. Measurements were conducted on the ORSIM Bronchoscopy simulator using its own measurement parameters, including Task Completion Time (s), Collision Avoidance (%), and Final Score (min 0-100). A decrease in task completion time, an increase in collision avoidance percentage, and a higher final score indicate that the participant performed fiberoptic intubation more effectively.
During FOE simulation

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)

November 15, 2023

Primary Completion (Actual)

November 17, 2023

Study Completion (Actual)

December 15, 2023

Study Registration Dates

First Submitted

November 13, 2023

First Submitted That Met QC Criteria

November 13, 2023

First Posted (Actual)

November 18, 2023

Study Record Updates

Last Update Posted (Actual)

March 19, 2024

Last Update Submitted That Met QC Criteria

March 18, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • GenderAndFob

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Time Frame

at the and of the study

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

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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