Non-technical Skills Training and Checklists Versus Standard Training With Checklists for Prevention of Medical Error

NCT ID: NCT04621682

Last Updated: 2022-03-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

86 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-03-20

Study Completion Date

2021-08-01

Brief Summary

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The purpose of this study is to reduce medical error by omitting management steps in medical crises. The Interventions will be: training in non-technical skills and checklists versus Control: standard training with checklists

Detailed Description

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56 participants will be searched for simulation training, randomly assigned in assignment 1 to 1, the follow-up will be 10 days, the primary outcome will be Proportion of omissions of treatment steps per group, and secondary outcomes will be sought. Crisis resolution time, detection time. and discrimination from the crisis Global score of non-technical skills, Discriminated score between dimensions of non-technical skills, Student satisfaction and Incidence of inadequate crisis management.

Conditions

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Medical Emergencies

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

TECRISIS is a study designed as a controlled clinical trial of superiority with parallel groups, random allocation and blinding of investigators who measure outcome.
Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Non technical skills and check list

10 hours of training in non-technical skills and checklists in high Fidelity simulation

Group Type ACTIVE_COMPARATOR

Non technical skills and checklist training in simulation

Intervention Type OTHER

using structured debrifing, in three random medical simulation crises, training in non-technical skills will be carried out

check list

Control: 10 hours of standard training with checklists in high Fidelity simulation

Group Type ACTIVE_COMPARATOR

Checklist training simulation

Intervention Type OTHER

using structured debrifing, in three random medical simulation crises, training in checklist will be carried out

Interventions

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Non technical skills and checklist training in simulation

using structured debrifing, in three random medical simulation crises, training in non-technical skills will be carried out

Intervention Type OTHER

Checklist training simulation

using structured debrifing, in three random medical simulation crises, training in checklist will be carried out

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* over 18 years old.
* Final semester student of medicine at the University of Antioquia.
* Have passed the theoretical knowledge exam for handling crisis events with a score of 100%.
* On-site availability on training days

Exclusion Criteria

* Having received training in a specific crisis resource management course.
* Refusing to participate
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Universidad de Antioquia

OTHER

Sponsor Role lead

Responsible Party

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Mario Zamudio

Clinical Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Mario Andres Zamudio

MedellĂ­n, Antioquia, Colombia

Site Status

Countries

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Colombia

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

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F070

Identifier Type: -

Identifier Source: org_study_id

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