AzTrials
AzTrials

Communication BarriersNCT06322004

Video-Interpreting in Prehospital Emergency Medicine - Feasibility Study

An observational study of Communication Barriers, run by Medical University of Vienna at 1 site in Austria.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

50 responsive patients with language barriers will be included in this study. The prehospital emergency physician will start video-interpreting via a tablet. Feasibility, quality of communication, usability as well as changes in diagnosis and treatment will be gathered and analysed. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Communication Barriers
How many people
50 participants
Where
1 siteAustria
Study dates
6 Feb 2023to 31 Dec 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Adult, Older adult

Study population: 50 responsive patients treated by prehospital emergency doctors of the Department of Anaesthesia, Intensive Care and Pain Management (Medical University of Vienna/ General Hospital of Vienna) with language barrier (14 languages Albanian, Dari, Romanian, Turkish, Modern Standard Arabic, Arabic, Farsi, Russian, Hungarian, Bosnian-Croatian-Serbian, Kurdish (Kurmanci), Slovakian, Bulgarian, Polish, and Czech) will be included regarding inclusion and exclusion criteria mentioned above.

Who may be able to join

  • adult patients, at least 18 years old
  • awake, responsive patients
  • language barrier (Albanian, Dari, Romanian, Turkish, Modern Standard Arabic, Arabic, Farsi, Russian, Hungarian, Bosnian-Croatian-Serbian, Kurdish (Kurmanci), Slovakian, Bulgarian, Polish, and Czech)

Who cannot join

  • unconscious patients
  • out-of-hospital cardiac arrest patients
  • delay of treatment or transportation due to e-interpreting
  • refusal of video-interpreting by the patient

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Maike Fink, Dr.med.univ. contact

01/40400 41000

maike.fink@meduniwien.ac.at

Christina Hafner contact

christina.hafner@meduniwien.ac.at

Austria1 site, 1 recruiting
  • Medical University of Vienna

    Vienna, 1090

    Christina Hafner, DDr., christina.hafner@meduniwien.ac.at

    Maike Fink, Dr.med.univ.

    Recruiting

Other trials in Austria

About this study

50 responsive patients with language barriers will be included in this study. The prehospital emergency physician will start video-interpreting via a tablet. Feasibility, quality of communication, usability as well as changes in diagnosis and treatment will be gathered and analysed.

Keywords
Communication barriers, Prehospital emergency medicine, Emergency medicine, Emergency physician

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Technical Feasibility

    The technical feasibility endpoint evaluates the possibility of video-interpreting.

    The occurrence of technical problems will be reported.

    Measured: Immediately after use of video-interpreting

  2. Usability of video-interpreting

    The usability will be evaluated after the rescue mission by the prehospital emergency doctor using a questionnaire including following items on a 7-point Likert scale (strongly disagree to strongly agree):

    • Video-translation was easy to use.
    • I feel comfortable to use video-translation during the situation.
    • The amount of time involved to use video-translation has been fitting for me.
    • I would use video-translation again.
    • Video-translation was useful for my healthcare practice in this situation.

    Measured: Immediately after use of video-interpreting

  3. Impact on emergency physician's decisions

    The impact of video-translation will be evaluated regarding alteration of medical history, treatment or target hospital.

    Measured: Immediately after use of video-interpreting

Secondary outcomes (1)
  1. Demographic parameters

    Following characteristics of the patients will be recorded:

    Age, Gender, primary diagnosis of the prehospital emergency physician

    Measured: Immediately after use of video-interpreting

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Mar 2024
  2. Study start6 Feb 2023
  3. Primary completion31 Dec 2026 (estimated)
  4. Study completion31 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Prospective
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06322004
Sponsor's protocol ID
1718/2022
Status last verified
Oct 2025
First submitted
25 Oct 2023
Last updated
20 Apr 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Communication Barriers, run by Medical University of Vienna at 1 site in Austria.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 20 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Austria. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Maike Fink, Dr.med.univ. (01/40400 41000, maike.fink@meduniwien.ac.at), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Technical Feasibility (time frame: Immediately after use of video-interpreting). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Apr 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in