Potential Optimization Training in Simulation.

Healthy Clinical Trial

— TOP  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02926599
• Other study ID #: TOPCLESS
• Status: Completed
• Phase: N/A
• Start date: September 2016
• Est. completion date: October 2017

Study information

• Verified date: August 2018
• Source: Claude Bernard University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 118
• Est. completion date: October 2017
• Est. primary completion date: September 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Anesthesiology and Intensive care resident in the simulation education curriculum

Exclusion Criteria:

• Refusal to participate (written approval required)

Related Conditions & MeSH terms

• Healthy

Intervention

Behavioral:
• Personal Optimization Training

Locations

Country	Name	City	State
France	CLESS	Lyon	Rhône-Alpes

Sponsors (1)

Lead Sponsor	Collaborator
Claude Bernard University

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	psychometric POMS scales	psychometric POMS scales	day 1
Other	psychometric STAI scales	psychometric STAI scales	day 1
Primary	Performance during simulation	Performance 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.	day 1
Secondary	visual analogic scale of anxiety	Visual analogic scales of anxiety	day 1
Secondary	Visual analogic scales of confidence	Visual analogic scales of confidence	day 1