Skip to content

Potential Optimization Training in Simulation.

High Fidelity Simulation Performance After a Potential Optimization Training for Anesthesiologist Resident: a Randomized Controlled Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02926599
Acronym
TOP
Enrollment
118
Registered
2016-10-06
Start date
2016-09-30
Completion date
2017-10-31
Last updated
2018-08-21

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

Conditions

Healthy

Keywords

High Fidelity Simulation

Brief summary

Simulated environment allowed safe learning of critical events and knowledge of appropriate response and treatment. Anesthesiology resident education curriculum in Lyon plans several high fidelity simulation session with a large panel of critical events. Anticipation of critical events before they may occur and planification of team resources and priority in the treatment strategy may help to improve team performance during the scenario. The investigators' goal is to compare individual and team performances with or without an optimization personal potential training.

Detailed description

The investigators aim to compare the individual and team performances for resident who were taught personal optimization skills (positive reinforcement, personalized psycho-physiological relaxation, mental rehearsal) and those who didn't. The investigators are going to compare groups of anesthesiology residents going through same scenarios of simulated critical events in high fidelity simulation session. Scenarios will be recorded to be analyzed by 2 reviewers independently. A specific checklist of appropriate treatment and a non technical skill checklist will be use to cote team performance (OTTAWA and TEAM scales). Stress of the participants will be assessed by visual analogic scale of participants anxiety and stress. The two groups will be compare to see if improvement in team performance is associated with the intervention.

Interventions

BEHAVIORALPersonal Optimization Training

Sponsors

Claude Bernard University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Anesthesiology and Intensive care resident in the simulation education curriculum

Exclusion criteria

* Refusal to participate (written approval required)

Design outcomes

Primary

MeasureTime frameDescription
Performance during simulationday 1Performance will be assessed by the sum of 3 assessment: Ottawa non technical skill scale, team scanle and specific technical skill scale Total will be a number from 0 to 100.

Secondary

MeasureTime frameDescription
visual analogic scale of anxietyday 1Visual analogic scales of anxiety
Visual analogic scales of confidenceday 1Visual analogic scales of confidence

Other

MeasureTime frameDescription
psychometric POMS scalesday 1psychometric POMS scales
psychometric STAI scalesday 1psychometric STAI scales

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026