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RecruitingNCT06570681Updated Sep 30, 2026

Video Call Assisted Assessment of Acute Stroke

An interventional study of Video call assisted assessment of acute stroke in Stroke, Cerebrovascular Disorders and Brain Diseases, sponsored by University of Southern Denmark. Recruiting at 1 site in Denmark. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-30.

Sponsored by University of Southern Denmark · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
512
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

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.

Read the detailed description

Treatment of stroke with either thrombolysis or thrombectomy is highly time-dependent (administration within 4.5 hours and 24 hours from symptom onset, respectively), and morbidity and mortality increase with time from symptom onset to treatment. Hence, prehospital evaluation and transport must be as accurate and rapid as possible in order to minimise time to treatment.

Different triage and transport paradigms for patients with suspected stroke are being investigated and multiple stroke scales have been coined in order to examine patients suspected of stroke in a prehospital setting. However, performance and feasibility vary greatly in different validation studies suggesting that those outcomes are greatly dependent on other factors i.e. acceptance amongst stakeholders, implementation process, patient segment etc. Some recent studies have shown promising results using video solutions between emergency medical services (EMS) personnel and on-call neurologist in examining patients suspected of stroke in the prehospital phase. The investigators will perform this trial to examine whether a video call assisted assessment of patients suspected of stroke in a prehospital setting can increase feasibility and performance of symptom-based prehospital stroke scales.

02

Conditions studied

  • Stroke
  • Cerebrovascular Disorders
  • Brain Diseases
  • Nervous System Diseases
  • Vascular Diseases
  • Central Nervous System Diseases
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Suspected stroke within 24 hours from onset (confirmed with Prehospital Stroke 1 decision tool)
  • Age >18 years

Exclusion criteria

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)
04

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
512 participants (estimated)

Study arms

  • No intervention
    Standard Care

    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. If the vehicle is in the control arm the patient is triaged by the on-call neurologist based on a standard telephone call

  • Active comparator
    Video call assisted assessment of acute stroke

    If the patient is eligible for study inclusion, the last 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 the video-call and triage the patient.

    Diagnostic Test: Video call assisted assessment of acute stroke

Interventions

  • Diagnostic testVideo 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.

05

What researchers measure

Primary outcomes

  1. Acute ischemic stroke (AIS) or transient ischemic attack (TIA) diagnosis at discharge

    AIS or TIA as diagnosis. (binary outcome)

    Time frame: At discharge, assessed within one week from symptom onset

Secondary outcomes

  1. Number of patients with acute ischemic stroke (AIS) with LVO on neuroimaging

    AIS with LVO on neuroimaging (computer tomography (CT), CT angiography, magnetic resonance imaging (MRi), MR angiography or catheter-based angiography). LVO is defined as a occlusion or sub-occlusion of the intracranial internal carotid artery, middle cerebral artery M1 or M2, basilar artery. Sign of dense cerebral artery on CT is also considered LVO positive. (binary outcome).

    Time frame: Within 48 hours of admission

  2. Number of patients with Other large vessel AIS

    Neuroimaging (computer tomography (CT), CT angiography, magnetic resonance imaging (MRi), MR angiography or catheter-based angiography) with AIS with occlusion or sub-occlusion of either anterior cerebral artery A1 or A2, posterior cortical artery P1 or intracranial vertebral artery (binary outcome).

    Time frame: at admission

  3. Number of patients with verified acute ischemic stroke (AIS) on neuroimaging

    Neuroimaging (computer tomography (CT), CT angiography, magnetic resonance imaging (MRi), MR angiography or catheter-based angiography) with AIS

    Time frame: Within 48 hours of admission

  4. Number of patients with Haemorrhagic stroke

    Neuroimaging (computer tomography (CT), CT angiography, magnetic resonance imaging (MRi), MR angiography or catheter-based angiography) with intra cranial haemorrhage (ICH) (binary outcome)

    Time frame: at admission

Other outcomes

  1. Duration of examination on video-call

    Duration of examination on video-call measured in minutes (continuous outcome)

    Time frame: up to 120 minutes prior to admission (prehospital phase)

  2. Number of patients which have mimic mistaken for stroke

    Mimic mistaken for stroke evaluated as discrepancy between stroke as tentative diagnoses at primary contact from EMS and final diagnosis at discharge

    Time frame: Through study completion, approximately 2 months

  3. Prehospital time on scene

    Time on scene from arrival EMS to departure EMS measured in minutes (continuous outcome)

    Time frame: up to 120 minutes prior to admission (prehospital phase)

  4. Type of department patient is admitted to after consultation with the neurologist

    Where was the patient sent after telephone/video consultation with the on-call neurologist.

    Time frame: At admission

  5. Door-in-door-out (DIDO) time

    DIDO times for patients subsequently sent to comprehensive stroke unit for thrombectomy treatment.

    Time frame: at admission

  6. Door-to-needle (DNT) time

    DNT times for patients receiving thrombolysis

    Time frame: at admission

  7. Door-to-Groin-Puncture (DTGP) time

    DTGP times for patients receiving treatment with thrombectomy

    Time frame: within 24 hours of admission

  8. Onset-to-Groin-Puncture (OTP) time

    OTP for patients receiving treatment with thrombectomy

    Time frame: within 24 hours of admission

  9. 90 days modified Ranking Scale (mRS)

    Modified Rankin Scale score in stroke patients as evaluated through a structured telephone-based interview performed by a central assessor who is blinded to group assignment

    Time frame: 90 days post admission date

06

Study locations

1 of 1 sites recruiting
  • Department of Neurology
    Aabenraa, Region Syddanmark 6200, Denmark
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06570681
Lead sponsor
University of Southern Denmark
Responsible party
Sponsor
First posted
Aug 26, 2024
Start date
May 27, 2024
Primary completion
Dec 1, 2026 (estimated)
Completion
Dec 3, 2026 (estimated)
Last update
Sep 30, 2026

Study contacts

Trine Nielsen
Contact
Trine.Nielsen2@rsyd.dk
+45 79 97 00 00
Christian Backer Mogensen
Contact
CBM1@rsyd.dk
+45 79 97 00 00

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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