Simulation to Assess Cognitive Workload and Task Load IndeX (TLX) Performance
NCT ID: NCT03175484
Last Updated: 2018-07-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
84 participants
OBSERVATIONAL
2017-06-01
2017-12-22
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The complexity of instructional design may produce cognitive overload, high stress level and anxiety. This may increase fatigue, facilitate errors, and is associated with inferior task performance which may impede memorization of learned skills resulting in inefficient learning/simulation failure. Subjectively reported scales can accurately identify the level of perceived workload and mental demand in individuals during simulation tasks. One example is the National Aeronautics and Space Administration (NASA)-TLX - the most accepted subjective measure of human workload in various industries including medicine.
Surgical specialty (including anesthesia) and nurses training curriculum in Lyon, France, includes several HFS scenarios with a large panel of critical events. The investigators aim to evaluate the effect of burden of workload and stress perceived by surgical specialty (including anesthesia) residents and nurses during HFS on the learning performance, and to grade different learning scenarios by their difficulty.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Performance and Team Pre-critical Staff Before Critical Event in High Fidelity Simulation for Anesthesiology Residents
NCT02599584
Potential Optimization Training in Simulation.
NCT02926599
Evaluation of a Simulation Based Workshop in an Anesthesia Residency Program
NCT03545984
Simulation-based Learning for Neurosurgical Instruments in Perioperative Nurses
NCT03894644
Effectiveness of Simulation With Nursing Students in the Care of Patients With Sepsis
NCT04512183
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Two investigators will independently evaluate the performance of HFS by direct observation and video record if necessary. NASA TLX questionnaire will be administrated immediately after HFS scenario and before the debriefing. Anxiety scale and pupillometry will be administrated before the beginning of HFS scenario and upon its completion.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Observation TLX
surgical specialty ( including anesthesia) residents and nurses undergoing High Fidelity Simulation scenarios.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Enrolled in surgical specialty (including anesthesia) simulation training program
or
* Lyon Anesthesia Nurses School student status on the day of the study
* Enrolled in surgical specialty (including anesthesia) simulation training program
* voluntary
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Claude Bernard University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Lilot Marc
MD
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Marc Lilot, MD
Role: PRINCIPAL_INVESTIGATOR
CLESS
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
CLESS
Lyon, Auvergne-Rhône-Alpes, France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
HFS-TLX-Lyon
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.