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Recruiting Not applicable

Video Call Assisted Assessment of Acute Stroke

NCT06570681 · tracked via the Priya Life Science Denmark tracker
Phase
Not applicable
Started
2024-05-27
Last updated
2026-09-30

Condition(s) studied

StrokeCerebrovascular DisordersBrain DiseasesNervous System DiseasesVascular DiseasesCentral Nervous System Diseases

Investigational drug(s) / intervention(s)

Video call assisted assessment of acute stroke

Video call assisted assessment of acute stroke: If the patient is eligible for study inclusion, eight symptoms from the study protocol are evaluated and registered in the Prehospital Patient Journal (PPJ) on the amPHITM Prehospital Health Care Record (Amphi Systems, Hasserisvej 125, 9000 Aalborg, Denmark), on a tablet mounted in each EMT vehicle. Afterwards, the EMS personnel will contact the on-call neurologist and if the vehicle is in the intervention arm a live video stream is initiated. The on-call neurologist then examines the patient via via the video-call and triages the patient.

Study summary

This study aims to investigate whether a live stream video between the on-call neurologist and the emergency medical technicians can increase feasibility and performance of symptom-based prehospital stroke scales.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Suspected stroke within 24 hours from onset (confirmed with Prehospital Stroke 1 decision tool) * Age \>18 years Exclusion Criteria: * Suspected stroke more than 24 hours ago * In-hospital stroke or private transport to hospital * Unconsciousness defined as Glasgow Coma Score (GCS) ≤ 8 (as they cannot be rated)

Primary outcome measure(s)

  • Acute ischemic stroke (AIS) or transient ischemic attack (TIA) diagnosis at discharge — At discharge, assessed within one week from symptom onset
    AIS or TIA as diagnosis. (binary outcome)

Trial sites (1)

FacilityCityRegionStatus
Department of Neurology Aabenraa Region Syddanmark Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06570681 on ClinicalTrials.gov ↗ ← All trials in Denmark