Dispatcher-Assisted CPR: Low-Dose, High-Frequency Simulation-Based Training
NCT ID: NCT04085692
Last Updated: 2020-01-23
Study Results
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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COMPLETED
NA
52 participants
INTERVENTIONAL
2019-09-12
2019-12-25
Brief Summary
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The study is a randomised controlled trial comparing LDHF simulation-based training to standard quality improvement of the EMD in a single centre. The study protocol is structured according to the SPIRIT 2013 statement, and the study will be reported in compliance with the CONSORT 2010 Statement. The investigators chose EMDs receiving standard quality improvement as the comparator group, to reflect a representative cohort of the EMDs not exposed to the LDHF simulation-based training program.
The aims of this study are:
1. To measure the effect of LDHF simulation-based training on the quality of DA-CPR in a simulation setting.
2. To measure the effect of LDHF simulation-based training on the quality of DA-CPR in real OHCA calls.
The investigators hypothesise that LDHF simulation-based training will increase the quality of DA-CPR in the intervention group in a simulation setting and that this improvement is transferred to real OHCA calls - although the effect in real OHCA calls might be smaller due to the complexity of some calls. The investigators hypothesise that this improvement can be detected as a decrease in time to first bystander compression (TTFC), an increase in clarification of consciousness and breathing without asking additional questions, a decrease in time to recognition of cardiac arrest, and an increase in calls where the EMD provide DA-CPR instructions on patients in cardiac arrest.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
The EMDs will be randomly assigned to intervention or comparison group in a 1:1 ratio.
Randomisation will be stratified by the EMDs' medical backgrounds (paramedic, approximately 30% of the EMDs, or registered nurse, approximately 70% of the EMDs), to balance the number of EMDs with different medical backgrounds randomly assigned to each arm.
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
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Intervention
The intervention group begins LDHF dispatcher training with one introduction week followed by twelve weeks of LDHF training.
During the study period, all regular quality improvement (QI) activities, such as self-audits, case reviews, mentor groups, and status meetings will continue for all EMDs.
Low-Dose, High-Frequency Simulation-Based Training
Twelve weeks of LDHF training
The simulation-based training sessions take place at the EMDC, at extra workstations set-up as ordinary EMD workstations in an out-of-the-way area. Before each session, the EMD is informed about the simulation call and receives instructions concerning technical differences from a regular call. The instructor acts as a "standardised caller", guided by a computer program. This program, the Danish version of Resuscitation Quality Improvement for Telecommunicators (Laerdal Medical AS, Stavanger, Norway), is a training program for DA-CPR based on the simulation platform Laerdal Learning Application. This modified version of the RQI-T program has, one test scenario, one data collection scenario and six different cardiac arrests scenarios as well as a feedback checklist based on the Danish dispatcher protocol Danish Index for Emergency Care.
Each simulation session takes approximately 20 minutes, including introduction and feedback
Comparison
During the study period, all regular quality improvement (QI) activities, such as self-audits, case reviews, mentor groups, and status meetings will continue for all EMDs.
No interventions assigned to this group
Interventions
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Low-Dose, High-Frequency Simulation-Based Training
Twelve weeks of LDHF training
The simulation-based training sessions take place at the EMDC, at extra workstations set-up as ordinary EMD workstations in an out-of-the-way area. Before each session, the EMD is informed about the simulation call and receives instructions concerning technical differences from a regular call. The instructor acts as a "standardised caller", guided by a computer program. This program, the Danish version of Resuscitation Quality Improvement for Telecommunicators (Laerdal Medical AS, Stavanger, Norway), is a training program for DA-CPR based on the simulation platform Laerdal Learning Application. This modified version of the RQI-T program has, one test scenario, one data collection scenario and six different cardiac arrests scenarios as well as a feedback checklist based on the Danish dispatcher protocol Danish Index for Emergency Care.
Each simulation session takes approximately 20 minutes, including introduction and feedback
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Planned employment cessation at the Copenhagen EMS during the data collection period.
* Planned leave from work longer than four weeks during the data collection period.
* Starting employment at the Copenhagen EMS during the study period.
ALL
Yes
Sponsors
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TrygFonden, Denmark
INDUSTRY
Emergency Medical Services, Capital Region, Denmark
OTHER_GOV
Responsible Party
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Principal Investigators
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Freddy Lippert, MD
Role: PRINCIPAL_INVESTIGATOR
Emergency Medical Services, Capital Region, Denmark
Oscar Rosenkrantz
Role: STUDY_DIRECTOR
Emergency Medical Services, Capital Region, Denmark
Locations
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Copenhagen Emergency Medical Services
Copenhagen, , Denmark
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan: Full protocol
Document Type: Informed Consent Form
Document Type: Study Protocol: Supplementary assessment points for table 1
Other Identifiers
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DTP
Identifier Type: -
Identifier Source: org_study_id
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