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Use of a Wearable Digital Cognitive Aid in Simulated Anesthesia and Intensive Care Crises.

Use of a Wearable Digital Cognitive Aid in Simulated Anesthesia and Intensive Care Crises.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02678819
Acronym
SIMMAX
Enrollment
52
Registered
2016-02-10
Start date
2015-07-31
Completion date
2016-04-30
Last updated
2016-07-26

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

Conditions

Cognitive Aids

Brief summary

The purpose of this study is to determine whether a wearable digital cognitive aid has an effect in the management of simulated crises in anesthesia or intensive care.

Detailed description

Errare humanum est , to err is human. This Latin saying attributed to Seneca shows that since the dawn of time, human beings are aware that managing complex situations will always be an inexhaustible source of mistakes. This is particularly true in anesthesia and intensive care in which situations are often complex and stressful, thus leading to mistakes or inadequate management. Improvement might arise from the use of cognitive aids. The investigators designed a smartphone application including 5 scenarios of anesthesia and intensive care crises (malignant hyperthermia, anaphylactic shock, acute toxicity of local anesthetics, severe and symptomatic hyperkaliemia, ventricular fibrillation), easy to use with a manual validation of every simple step. Investigators seek to compare the technical and non technical management of these crises with and without this wearable cognitive aid.

Interventions

DEVICEDigital cognitive aid

Digital cognitive aid during anesthesia and intensive care crises.

Sponsors

CEJKA Jean-Christophe
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Resident Physicians training in Anesthesia/Intensive care (same specialization in France), year 2 to 5 (out of 5)

Exclusion criteria

* All other residents, including Resident Physicians training in Anesthesia/Intensive care, year 1 (out of 5)

Design outcomes

Primary

MeasureTime frameDescription
Technical Performance as compared to a Reference Task ListTime 0-30 minNumber of tasks successfully performed, rated on remote video review

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026