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

Sponsor
University of Southern Denmark (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05737420
Collaborator
(none)
40
1
2
4.9
8.1

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Video call
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Video-call Assisted Assessment of Acute Stroke in Addition to Stroke Severity Scales in a Prehospital Setting: A Cluster Randomised Pilot Trial
Anticipated Study Start Date :
Feb 1, 2023
Anticipated Primary Completion Date :
Apr 1, 2023
Anticipated Study Completion Date :
Jul 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Interventional video call

All patients suspected of stroke in a prehospital setting are examined according to a prehospital stroke score. The emergency services personnel then contact the on-call neurologist and a live video stream is initiated. The on-call neurologist then examines the patient via the video-call.

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

No Intervention: Control with standard care

All patients suspected of stroke in a prehospital setting are examined according to a prehospital stroke score. The emergency services personnel then contact the on-call neurologist by telephone. .

Outcome Measures

Primary Outcome Measures

  1. Recruitment Rate [Through study completion, approximately 2 months]

    Rate of patients included in the trial amongst all patients screened

  2. Exclusion rate [Through study completion, approximately 2 months]

    rate of patients excluded from participation amongst all patients screened

  3. Attrition rate [Through study completion, approximately 5 months]

    rate of patients and data lost

  4. Adherence to protocol by the Emergency Medical Services [Baseline (Prehospital examination of patient conducted by Emergency Medical Services)]

    Evaluation of missing data in the clinical examination prehospital in Pre-hospital patient journal

  5. Adherence to protocol by the neurologist prehospital [Baseline (Prehospital examination of patient conducted on video by neurologists)]

    Evaluation of missing data in the clinical examination conducted with video

  6. Adherence to protocol by the neurologist intrahospital [At admission]

    Evaluation of missing data in the National Institute of Health Stroke Scale conducted intrahospital by neurologist

  7. Stakeholder Feedback Survey [immediately after the intervention]

    Mixed open-ended and closed (Likert type response) questions to assess trial and intervention acceptability

  8. Patient Feedback Survey [Between the day after admission and 5 days after admission]

    Semistructured interview with open-ended and closed (Likert type response) questions to assess intervention acceptability

Secondary Outcome Measures

  1. Acute ischemic stroke with Large Vessel Occlusion on neuroimaging [At admission]

    Acute 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.

  2. Other large vessel Acute ischemic stroke [at admission]

    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

  3. Other Acute ischemic stroke [at admission]

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

  4. Haemorrhagic stroke [at admission]

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

  5. Duration of examination on video-call [up to 60 minutes (prior to admission, prehospital phase)]

    Duration of examination on video-call measured in minutes

  6. Mimic mistaken for stroke [Through study completion, approximately 2 months]

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

  7. Prehospital time on scene [up to 60 minutes (at prehospital contact)]

    Time on scene from arrival of Emergency Medical Services to departure of Emergency Medical Services measured in minutes

  8. 90 days modified Rankin Scale [90 days post admission date]

    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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts 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)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sygehus Soenderjylland Aabenraa Denmark 6200

Sponsors and Collaborators

  • University of Southern Denmark

Investigators

  • Study Director: Christian Backer Mogensen, Hospital of Southern Denmark - Aabenraa

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of Southern Denmark
ClinicalTrials.gov Identifier:
NCT05737420
Other Study ID Numbers:
  • SHS-Neuro-1-2023
First Posted:
Feb 21, 2023
Last Update Posted:
Feb 21, 2023
Last Verified:
Feb 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 21, 2023