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Completed

NCT Number: NCT03724110

Telestroke for Comprehensive Transient Ischemic Attack Care in Acute Stroke Ready Hospitals

TELECAST-TIA is a prospective single-center study evaluating guideline-based transient ischemic attack (TIA) treatment at an Acute Stroke Ready Hospital (ASRH) pre- and post-initiation of a specialist telestroke inpatient rounding service. TELECAST-TIA will study the following clinical endpoints: diagnostic stroke evaluation, secondary stroke prevention, health screening and evaluation, stroke education, inpatient complications, and stroke recurrence rates. Additional relevant non-clinical data will include patient and provider satisfaction scores, transfer patterns, and a cost analysis.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Fairview Ridges Hospital, Burnsville, Minnesota, United States

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About this study

Telestroke is a validated intervention that improves the triage and emergent treatment of acute stroke, specifically related to the use of intravenous thrombolysis. Effective urgent stroke evaluation and secondary stroke prevention is also essential to decrease the risk of recurrent stroke, however, there have been no studies to date examining the use of telestroke to improve delivery of non-emergent inpatient stroke care per American Heart Association (AHA) guidelines.

Currently, access to stroke specialist expertise is limited resulting in significant disparities in stroke care. Previous publications have identified that patients in rural areas may receive sub-optimal stroke care that does not follow accepted guideline recommendations. Telestroke is a cost-effective mechanism to deliver specialist stroke care to hospitals that do not have in-person stroke consultation available. The aim of TELECAST-TIA is to determine whether specialist telestroke inpatient rounding improves guideline-based TIA treatment when compared to non-specialist transient ischemic attack treatment.

The primary outcome of TELECAST-TIA is a composite score of 3 categories: diagnostic stroke evaluation, secondary stroke prevention, and stroke education. Individual components of the primary outcome were principally derived from AHA stroke guidelines. Additional outcome measures include individual analyses of the components of the primary outcome as well as the complication rate, stroke recurrence rate, transfer rate, patient and provider satisfaction levels, and a cost-analysis. All outcomes will be assessed at 1 year post-implementation, with data accruement starting after a 3-month lead in phase.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 and above
  • Patients with the primary diagnosis of transient ischemic attack evaluated at the Fairview Ridges Hospital emergency room
  • Clinical diagnosis of transient ischemic attack by the treating stroke neurology service

Exclusion criteria

  • Patients less than 18 years old
  • Patients who leave the hospital against medical advice
  • Patients who are felt to have an alternative diagnosis

Treatment and study plan

Telestroke

Other

Telestroke is an audiovisual communication network that allows for coordination of stroke care from a distant 'hub' site (the telestroke provider location) to an originating 'spoke' site (patient location) in a HIPAA compliant fashion. In TELECAST-TIA, inpatient telestroke rounding will be used to oversee the urgent diagnostic TIA evaluation, secondary stroke prevention, and stroke education in patients admitted with TIA.

Other names: Telemedicine

Primary outcomes

  1. Composite score of TIA treatment (%)

    Time frame: 1 year after implementation of the inpatient telestroke service

    A 19-item global assessment of fundamental TIA treatment primarily informed by AHA guidelines/GWTG criteria, represented in 3 categories:

    • Diagnostic evaluation (10 items): neurologist evaluation, LDL, HgA1c, head CT, brain MRI, intracranial vascular imaging, cervical vascular imaging, EKG, telemetry, and outpatient prolonged cardiac monitoring.
    • Secondary prevention (6 items): antiplatelet, anticoagulation, statin, antihypertensives, diabetes management, and carotid revascularization.
    • Stroke education (3 items): tobacco cessation counseling, exercise/lifestyle counseling, and signs of stroke.

    An item is not scored when not indicated clinically (for example tobacco cessation in a non-smoker), therefore the composite scores will be reported and analyzed as percentages.

Secondary outcomes

  1. Diagnostic TIA Evaluation

    Time frame: 1 year after implementation of the inpatient telestroke service

    A 10-item global assessment of diagnostic TIA evaluation as well as individual analysis of each item.

    Diagnostic evaluation (10 items): neurologist evaluation, LDL, HgA1c, head CT, brain MRI, intracranial vascular imaging, cervical vascular imaging, EKG, telemetry, and outpatient prolonged cardiac monitoring.

    An item is not scored when not indicated clinically (for example prolonged cardiac monitoring in a patient with known Afib or an MRI in a patient with an MRI incompatible pacemaker), therefore the composite scores will be reported and analyzed as percentages.

  2. Secondary Stroke Prevention

    Time frame: 1 year after implementation of the inpatient telestroke service

    A 6-item global assessment of secondary stroke prevention as well as individual analysis of each item.

    Secondary stroke prevention (6 items): antiplatelet, anticoagulation, statin, antihypertensives, diabetes management, and carotid revascularization.

    An item is not scored when not indicated clinically (for example deferring antiplatelet agents if a patient requires anticoagulation), therefore the composite scores will be reported and analyzed as percentages.

  3. Stroke Education

    Time frame: 1 year after implementation of the inpatient telestroke service

    A 3-item global assessment of stroke education as well as individual analysis of each item.

    Stroke education (3 items): tobacco cessation counseling, exercise/lifestyle counseling, and signs of stroke.

    An item is not scored when not indicated clinically (for example tobacco cessation in a non-smoker), therefore the composite scores will be reported and analyzed as percentages.

  4. Composite Stroke Recurrence

    Time frame: Measured at 3 months and at 1 year after discharge

    The composite rate of recurrent TIA, ischemic, or hemorrhagic stroke at 3 months and one year post-stroke admission.

Other outcomes

  1. Admission rate

    Time frame: 1 year after implementation of the inpatient telestroke service

    Rate of admission versus discharge from the ED.

  2. Patient demographics

    Time frame: 1 year after implementation of the inpatient telestroke service

    Patient demographics of the TIA service will be assessed.

  3. Cost analysis

    Time frame: 1 year after implementation of the inpatient telestroke service

    A cost analysis incorporating the referring 'spoke' hospital and the central 'hub' hospital will be performed. Data collected will include hospital cost of admission, hospital admission reimbursement, transfer costs, and operational costs.

  4. Hospital length of stay

    Time frame: 1 year after implementation of the inpatient telestroke service

    The number of days of hospitalization for patients admitted with a primary diagnosis of TIA.

  5. Inpatient Telestroke Feasibility: Physician and Provider patient care time

    Time frame: 1 year after implementation of the inpatient telestroke service

    Total screen telestroke screen time will be assessed. This will be defined by the time that the telestroke patient visitation connection was made until it was terminated and also by the amount of time billed by the physician.

  6. Inpatient Telestroke Feasibility: Time from admission to consultation

    Time frame: 1 year after implementation of the inpatient telestroke service

    Time from both admission and consult order placement until consultation

  7. Composite score of fundamental TIA treatment at non-telestroke ASRHs (%)

    Time frame: 1 year after implementation of the inpatient telestroke service

    A 19-item assessment of fundamental TIA treatment (see primary outcome) at ASRHs within the same stroke network that do not have an inpatient telestroke service. These scores will serve as temporal controls for the primary outcome.

    An item is not scored if it is not indicated clinically (for example tobacco cessation in a non-smoker), therefore the composite scores will be reported and analyzed as percentages.

  8. Composite score of fundamental TIA treatment at the CSC hub site (%)

    Time frame: 1 year after implementation of the inpatient telestroke service

    A 19-item assessment of fundamental TIA treatment (see primary outcome) at the CSC hub site. This data will serve to compare the delivery of TIA treatment via telestroke vs. TIA treatment delivered in person at the hub site.

    An item is not scored if it is not indicated clinically (for example tobacco cessation in a non-smoker), therefore the composite scores will be reported and analyzed as percentages.

  9. Physician, Patient, Nursing satisfaction with Telestroke Rounding

    Time frame: 1 year

    Surveys will assess local physician, nursing, and patient satisfaction with the virtual telestroke service. Assessed items will include perceptions of convenience/inconvenience, quality of care provided, and satisfaction with the service relative to an in-person consulting service and/or transfer to a comprehensive stroke center for in-person consultation.

Sponsors and collaborators

Lead sponsor

University of Minnesota

Other

Registry information

Acronym: TELECAST-TIA

Important dates

Study start
2018
Primary completion
2019
Study completion
2022
First posted
Oct 30, 2018
Registry last updated
Oct 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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