NCT06322004

Brief 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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
7mo left

Started Feb 2023

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress83%
Feb 2023Dec 2026

Study Start

First participant enrolled

February 6, 2023

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

October 25, 2023

Completed
5 months until next milestone

First Posted

Study publicly available on registry

March 20, 2024

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

April 20, 2026

Status Verified

October 1, 2025

Enrollment Period

3.9 years

First QC Date

October 25, 2023

Last Update Submit

April 15, 2026

Conditions

Keywords

Communication barriersPrehospital emergency medicineEmergency medicineEmergency physician

Outcome Measures

Primary Outcomes (3)

  • Technical Feasibility

    The technical feasibility endpoint evaluates the possibility of video-interpreting. The occurrence of technical problems will be reported.

    Immediately after use of video-interpreting

  • 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.

    Immediately after use of video-interpreting

  • Impact on emergency physician's decisions

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

    Immediately after use of video-interpreting

Secondary Outcomes (1)

  • Demographic parameters

    Immediately after use of video-interpreting

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
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.

You may qualify if:

  • 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)

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Medical University of Vienna

Vienna, 1090, Austria

RECRUITING

Central Study Contacts

Maike Fink, Dr.med.univ.

CONTACT

Christina Hafner

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

October 25, 2023

First Posted

March 20, 2024

Study Start

February 6, 2023

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

April 20, 2026

Record last verified: 2025-10

Data Sharing

IPD Sharing
Will not share

Locations