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Video-call Assisted Assessment of Acute Stroke in Addition to Stroke Severity Scales in a Prehospital Setting

Video-call Assisted Assessment of Acute Stroke in Addition to Stroke Severity Scales in a Prehospital Setting: A Cluster Randomised Pilot Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05737420
Enrollment
33
Registered
2023-02-21
Start date
2023-07-06
Completion date
2024-01-30
Last updated
2024-05-31

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

Conditions

Brain Diseases, Central Nervous System Diseases, Cerebrovascular Disorders, Nervous System Diseases, Stroke, Vascular Diseases

Brief summary

This study aims to investigate whether a live stream video between the on-call neurologist and the emergency medical services is feasible.

Detailed description

Multiple stroke severity scales have been coined in order to examine patients suspected of stroke in a prehospital setting in order to identify and transfer patients eligible for thrombectomy directly to a comprehensive stroke centre (CSC). 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 telemedicine i.e. 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 cluster randomised trial with video call assisted assessment of patients suspected of stroke in a prehospital setting is an appropriate trial design and feasible with regard to recruitment and retention, acceptability among stakeholders (EMS and neurologists) as well as patients and lastly with regard to stakeholders' adherence to protocol.

Interventions

DIAGNOSTIC_TESTVideo call

The on-call neurologist can see and communicate with the patient via live stream video-call.

Sponsors

University of Southern Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Suspected stroke within 24 hours from onset (confirmed with Pre-hospital stroke score 1 ≥1) * Catchment area of Hospital Sønderjylland * Deferred informed consent obtained from patient or patient surrogate

Exclusion criteria

* In-hospital stroke or private transport to hospital * Unconsciousness defined as Glascow Coma Score (GCS) ≤ 8 (as they cannot be rated)

Design outcomes

Primary

MeasureTime frameDescription
Patient Feedback SurveyBetween the day after admission and 5 days after admissionSemistructured interview with open-ended and closed (Likert type response) questions to assess intervention acceptability
Recruitment RateThrough study completion, approximately 2 monthsRate of patients included in the trial amongst all patients screened
Exclusion rateThrough study completion, approximately 2 monthsrate of patients excluded from participation amongst all patients screened
Attrition rateThrough study completion, approximately 5 monthsrate of patients and data lost
Adherence to protocol by the Emergency Medical ServicesBaseline (Prehospital examination of patient conducted by Emergency Medical Services)Evaluation of missing data in the clinical examination prehospital in Pre-hospital patient journal
Adherence to protocol by the neurologist prehospitalBaseline (Prehospital examination of patient conducted on video by neurologists)Evaluation of missing data in the clinical examination conducted with video
Adherence to protocol by the neurologist intrahospitalAt admissionEvaluation of missing data in the National Institute of Health Stroke Scale conducted intrahospital by neurologist
Stakeholder Feedback Surveyimmediately after the interventionMixed open-ended and closed (Likert type response) questions to assess trial and intervention acceptability

Secondary

MeasureTime frameDescription
Acute ischemic stroke with Large Vessel Occlusion on neuroimagingAt admissionAcute ischemic stroke with Large Vessel Occlusion (LVO) on neuroimaging (computer tomography (CT), CT angiography, magnetic resonance imaging (MRi), MR angiography or catheter-based angiography). LVO is defined as an occlusion or sub-occlusion of the intracranial internal carotid artery, middle cerebral artery M1 or M2, basilar artery. Sign of a dense cerebral artery on CT is also considered LVO positive.
Other large vessel Acute ischemic strokeat admissionNeuroimaging (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
Other Acute ischemic strokeat admissionNeuroimaging (computer tomography (CT), CT angiography, magnetic resonance imaging (MRi), MR angiography or catheter-based angiography) with Acute ischemic stroke
Haemorrhagic strokeat admissionNeuroimaging (computer tomography (CT), CT angiography, magnetic resonance imaging (MRi), MR angiography or catheter-based angiography) with intra cranial haemorrhage (ICH)
Duration of examination on video-callup to 60 minutes (prior to admission, prehospital phase)Duration of examination on video-call measured in minutes
Mimic mistaken for strokeThrough study completion, approximately 2 monthsMimic mistaken for stroke evaluated as discrepancy between stroke as tentative diagnoses at primary contact from EMS and final diagnosis at discharge
Prehospital time on sceneup to 60 minutes (at prehospital contact)Time on scene from arrival of Emergency Medical Services to departure of Emergency Medical Services measured in minutes
90 days modified Rankin Scale90 days post admission dateModified 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

Countries

Denmark

Outcome results

None listed

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