NCT Number: NCT04127565
Implementation Strategy and Systemic Effects of Routine Telemedical Care in Prehospital Emergency Medicine
In two research projects a comprehensive prehospital telemedicine system was developed and general feasibility as well as impact on guideline adherence were evaluated. These results allowed stepwise implementation into medical routine care.
All steps and milestones from the research idea to implementation were analyzed and evaluated descriptively in this study. Using a pre-post intervention analysis the systemic effects of the implementation on change in emergency medical resource utilization were analyzed.
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Notify MeKey information
Sex eligibility
All sexes
Study type
Observational
About this study
In two interdisciplinary research projects a comprehensive prehospital telemedicine system was developed and general feasibility as well as impact on guideline adherence were evaluated. Feasibility and general safety were demonstrated. These results allowed stepwise implementation into medical routine care during a one year phase. During implementation positive effects on guideline adherence were found. Despite positive results there are many barriers that prevent implementation of research projects into routine medical care. Therefore, the current study evaluated and interpreted all steps and milestones from the research idea to implementation and evaluated them descriptively. Using a pre-post intervention analysis the systemic effects of the implementation on change in emergency medical resource utilization were analyzed. Resource utilization of physician staffed emergency medical service units was compared between a pre-implementation period (12 months, April 2013 - March 2014) and a post-implementation period (12 months, April 2015 - March 2016). During the pre-implementation period only standard care was available.
Inclusion criteria
All emergency medical service (EMS) missions in both periods.
Data sources: Electronic health records of the EMS missions (data pseudonymity) and database of the regional EMS dispatch center.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
All patients treated by emergency medical service during the pre- and post-implementation period.
Post-implementation period: Patients had to give verbal consent prior to teleconsultation.
Exclusion criteria
Pre-implementation period: none Post-implementation period: Patients who refused teleconsultation.
Treatment and study plan
Primary outcomes
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Change in usage of physician staffed EMS units
Time frame: Comparison between 1 year pre-implementation and 1 year post-implementation period.
Change in usage of physician staffed EMS units (ground based and helicopter based). Comparison between the pre- and post-implementation period.
Secondary outcomes
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Usage of telemedical support in the post-implementation period
Time frame: Through study completion in the post-implementation period (1 year)
Number of ambulance calls using telemedical support
-
Provided medications during teleconsultation
Time frame: Through study completion in the post-implementation period (1 year)
Number of delegated medications including opioids in the post-implementation phase
Sponsors and collaborators
Lead sponsor
RWTH Aachen University
Other
Registry information
Official study title
Implementation Strategy From Research to Routine Care of a Comprehensive Prehospital Telemedicine System and Pre-post Analysis of Systemic Effects
Important dates
- Study start
- 2013
- Primary completion
- 2016
- Study completion
- 2016
- First posted
- Oct 15, 2019
- Registry last updated
- Oct 15, 2019
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.