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Videoconferencing Between Ambulances and Physician at the Emergency Medical Dispatch Center, Effects on On-Site Patient Treatment and Patterns of Referral

Telemedical Solutions in Medical Emergencies, Advantages and Disadvantages for Patients, Healthcare Professionals, and Healthcare System. Study 2: Videoconferencing Between Ambulances and Physician at the Emergency Medical Dispatch Center,

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02095067
Enrollment
150
Registered
2014-03-24
Start date
2013-06-30
Completion date
2014-12-31
Last updated
2014-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Illness, Acute Injury

Keywords

Telemedicine, Emergency medical dispatch, Prehospital care, Video conference

Brief summary

The prehospital resources are limited. The emergency medical dispatch center (EMDC) is manned by qualified health care personnel around the clock. The investigators believe that the EMDC is an unexploited resource in the prehospital treatment of patients. By the use of videoconferencing the investigators will activate this resource. Mobile videoconferencing between ambulances and physician at the EMDC enables patient consultation at a distance. Video consultation between patient and the physician at the EMDC can take place when the patient is at home or in the ambulance. The primary aim of this study is to examine the effect of video consultation between physicians at the EMDC and patients receiving treatment by ambulance personnel on the number of patients receiving final treatment on-site in the pre hospital setting.

Interventions

Sponsors

Prehospital Medical Emergency Services, Aarhus, Central Denmark Region, Denmark
CollaboratorUNKNOWN
Central Denmark Region
CollaboratorOTHER
Aarhus University Hospital
CollaboratorOTHER
University of Aarhus
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Less ill/slightly injured patients receiving prehospital care by ambulance personnel

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frame
Number of patients receiving final treatment on-site prehospitallyFinal treatment is registered for the present consultation, assessed up 36 months, presented up to 36 months

Secondary

MeasureTime frameDescription
ReadmissionWithin 3 days of primary contact, assessed up to 36 months, presented up to 36 monthsFor all patients receiving consultation from physician at the dispatch center resulting in final treatment on-site, number of patients admitted to hospital within 3 days will be assessed.
Change in site of referralIf destination for patient is changed during consultataion with physician, assessed up to 36 months, presented up to 36 monthsIf the department to receive the patient is changed during consultation with physician at the dispatch center.
Number of treatments delivered by ambulance personnelThe number of treatments delivered by ambulance personnel during consultation with physician at the dispatch center, assessed up to 36 months, presented up to 36 months
Change of transportation modeIf mode of transportation is changed during consultation with physician, assessed up to 36 months, presented up to 36 monthsIf the mode of transportation is changed during consultation with physician at the dispatch center. Eg. from ambulance to standard patient transportation without monitoring og the possibility of treatment, ether with patient sitting up or lying down.

Other

MeasureTime frameDescription
Ambulance staff evaluation of usability of equipmentAt the time of using the equipment, asessed up to 36 months, presented up to 36 monthsIs investigated by the use of survey
Physicians evaluation of usability of equipmentAt the time of using the equipment, assessed up to 36 months, presented up to 36 monthsIs evaluated by the use of survey

Countries

Denmark

Contacts

Primary ContactNikolaj Raaber, MD
nikoraab@rm.dk23821085
Backup ContactIngunn Riddervold, MSc, PhD
Ingunn.Riddervold@ph.rm.dk78414912

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026