Simulation Training and Teamwork Concerning Intubation on the Icu

NCT ID: NCT04564105

Last Updated: 2023-03-15

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

104 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-09-04

Study Completion Date

2022-11-07

Brief Summary

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To assess effects of the simulation education on the group intubating patients in the iCU, in this prospective study investigators will video-record real-life intubations and simulations. From videos will be assessed correlation of technical and non-technical skills before and after the education and performance in real-life vs simulation intubation.

Detailed Description

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The aim of this trial is to study the effects of simulation education on the action of the group managing patient's airway in the intensive care unit (ICU). Before simulations investigators will video-record 20 real-world intubations. Consequently will be run simulations to whole staff of the ICU. After the education further 20 real-world intubations will be recorded. Also simulations are recorded. From the videos investigators assess technical and non-technical skills of the group before and after simulation education, correlations between groups and influence of the education on action of the group. On the first part of the study, hypothesis is that group's good non-technical skills improve also technical skills. On the second part of the study hypothesis is that performing well in simulation correlates with performing well in real-world situation and teams with less experience the correlation is stronger.

Conditions

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Airway Management

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Staff of the ICU

The whole staff (nurses and doctors) of the ICU will be recruited to this trial. When they give their informed consent, video-recording of the intubations will be started. After 20 videos, simulations will be run. Also simulations will be recorded. Thereafter 20 further real-life intubations will be recorded. Staff intubating patients before and after won't be same but they will be adjusted for experience related to intubations.

Group Type OTHER

simulation education

Intervention Type BEHAVIORAL

Intubation protocol will be trained by simulation exercise.

Interventions

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simulation education

Intubation protocol will be trained by simulation exercise.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

-intubations in the icu operated by staff who have given informed consent to this study

Exclusion Criteria

* intubations in the icu operated by anybody who have rejected video-recording
* intubations in the icu, when patient or patient being unable, close relative has denied permission to use video in this study
* intubated patient is a child, a prisoner, under military service, under forensic psychiatric evaluation, or patient can't give informed consent for example because of the cognitive impairment
* patient is isolated
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Turku

OTHER

Sponsor Role collaborator

Joint Authority for Päijät-Häme Social and Health Care

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Miretta Tommila

Role: PRINCIPAL_INVESTIGATOR

University of Turku

Locations

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PaijatHame Central Hospital

Lahti, , Finland

Site Status

Countries

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Finland

Other Identifiers

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0151/2020

Identifier Type: -

Identifier Source: org_study_id

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