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

NCT02678819 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2016-07-26

No results posted yet for this study

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.

Conditions

  • Cognitive Aids

Interventions

DEVICE

Digital cognitive aid

Digital cognitive aid during anesthesia and intensive care crises.

Sponsors & Collaborators

  • CEJKA Jean-Christophe

    lead OTHER

Principal Investigators

  • Jean-Christophe CEJKA, MD PhD mEng · Centre Lyonnais d'Enseignement par la Simulation en Santé, LYON

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-07-31
Primary Completion
2016-03-31
Completion
2016-04-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02678819 on ClinicalTrials.gov