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Effects of Stress on Observers and Their Subsequent Performance During High Fidelity Simulation-based Training.

Effects of Stress on Observers and Their Subsequent Performance During High Fidelity Simulation-based Training: A Randomized Controlled Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02211378
Enrollment
33
Registered
2014-08-07
Start date
2012-09-30
Completion date
2014-02-28
Last updated
2014-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress

Keywords

stress, performance, cortisol

Brief summary

This randomized controlled trial aims to determine if the stress response and performance of trainees who are observers in simulation training is similar to trainees who are actively participating in simulation training in the 'hotseat' during 3 consecutive simulation sessions. We hypothesize that trainees experience less stress when they are observers in the first 2 simulation sessions. However, when they are placed in the 'hotseat' during the third session, their stress response, as well as their performance, will be similar to trainees who spend all 3 simulation sessions in the 'hotseat'.

Detailed description

Background: High fidelity simulation-based training (SBT) using sophisticated manikins instead of real patients for medical teaching is now commonly practiced worldwide. We previously showed that SBT causes significant stress in the trainees, as evidenced by a rise in their heart rate and salivary cortisol(; and that repeated exposure to SBT was associated with the same level of stress, despite performance improving. From our studies, participants in the 'hot-seat' actively managing the clinical crisis experience the highest levels of stress but benefit the most from the learning experience. However, the stress experienced by observers (who are in the same room but not actively managing the crisis) and their learning outcomes have not been studied. Objectives: We aim to determine: 1) If observers of SBT experience less stress when compared to the trainees in the 'hot-seat' and; 2) if trainees who were observers in prior SBT sessions perform as well as trainees who were in the 'hot-seat' during subsequent SBT sessions. Methodology: Thirty-six trainee anaesthetists are randomized into 2 groups to undergo three SBT scenarios. 18 Trainees randomized to the Observer group will first undergo two SBT scenarios as observers followed by a third session in the 'hot-seat'. 18 Trainees in the Control group will undergo all 3 sessions in the 'hot seat'. For each session, stress response is measured by salivary cortisol and amylase while performance is measured using the Anaesthetists Non Technical Skills (ANTS) score. Clinical Significance: If we find that trainees who are observers of the first 2 SBT scenarios experience less stress than the 'hot-seat' trainees but yet achieve similar level of performance during the third SBT session, we can potentially make SBT less stressful and reduce the total number of simulation required, thus improving the efficiency of simulation training.

Interventions

Trainees are in the role of observers (not actively participating in simulation scenario) during first 2 simulation sessions, then placed in the role in the 'hotseat' actively participating during the third simulation session.

OTHERHotseat

Trainees in the hotseat group are placed in the 'hotseat' to actively participate and manage the simulated medical crises in the simulation scenarios.

Sponsors

Singhealth Foundation
CollaboratorOTHER_GOV
KK Women's and Children's Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
24 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Anaesthesia residents in their 2nd or 3rd year of training

Exclusion criteria

* Hypertension * Cardiac disease * Endocrine disorder * Use of beta-blockers * Recent stressful or traumatic life events * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Change in Salivary Cortisol from baselineFrom baseline to end of the simulation session, typically after 15 minutes.Salivary cortisol measurement. Saliva collected using Salimetric oral swabs and salivary cortisol measured using ELISA technique.

Secondary

MeasureTime frameDescription
Salivary amylaseFrom baseline to end of the simulation session, typically after 15 minutes.Saliva collected using Salimetric oral swabs and analyzed using ELISA technique
Anaesthetist's non-technical skills scoreDuring simulation, typically lasting 15 minutes.Anaesthetist's non-technical skills score: a validated and reliable marking system measuring non-technical skills comprising 4 elements including task management, teamwork, situation awareness and decision making.
DASS questionnaireAt the end of simulation sessionSubject's self assessment of stress using the Depression, Anxiety and Stress questionnaire

Countries

Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026