Stroke, Acute Clinical Trial
Official title:
Stroke Team Remote Evaluation Using a Digital Observation Camera Arizona - The Initial Mayo Clinic Experience
Noninvasive prospective multi-center study of an interactive 2-way, wireless or
site-independent, audiovisual telemedicine system designed for real-time remote examination
of acute stroke symptoms and deficits as a basis for treatment consultation and
recommendation.
Study aims (1) to determine the impact of a site-independent, remote, telemedicine
consultation system on decision making in the Emergency Department, regarding the decision
to treat or not to treat with thrombolytics; (2) to assess the numbers of patients who
receive thrombolytics and the time to treatment in patients evaluated by telemedicine versus
telephone only; (3) to assess the appropriateness of thrombolytic treatment decisions in
telemedicine versus telephone-only consultations; and (4) to assess the completeness of the
data collection in telemedicine versus telephone-only consultations.
60 patients in Arizona with acute presentation of stroke symptoms, per bedside practitioner
discretion (onset generally less than 12 hours and likely less than 3 hours)
Two arms: Video Camera/Telemedicine (Intervention n = 30) and No Video Camera/Telephone only
(Control n = 30)
Design
Noninvasive prospective multi-center study of an interactive 2-way, wireless or
site-independent, audiovisual telemedicine system designed for real-time remote examination
of acute stroke symptoms and deficits as a basis for treatment consultation and
recommendation.
Study aims (1) to determine the impact of a site-independent, remote, telemedicine
consultation system on decision making in the Emergency Department, regarding the decision
to treat or not to treat with thrombolytics; (2) to assess the numbers of patients who
receive thrombolytics and the time to treatment in patients evaluated by telemedicine versus
telephone only; (3) to assess the appropriateness of thrombolytic treatment decisions in
telemedicine versus telephone-only consultations; and (4) to assess the completeness of the
data collection in telemedicine versus telephone-only consultations.
60 patients in Arizona with acute presentation of stroke symptoms, per bedside practitioner
discretion (onset generally less than 12 hours and likely less than 3 hours)
Two arms: Video Camera/Telemedicine (Intervention n = 30) and No Video Camera/Telephone only
(Control n = 30)
Assessments
All cases will undergo the following assessments:
Patient-Level Visits
Baseline: Pre-stroke Modified Rankin Scale (demographics), pre-treatment Modified Rankin
Scale, medications during prior 3 days, physical exam and vital signs, NIHSS, Modified
NIHSS, EKG, screening labs, and head CT scan
Treatment: Treatment times, thrombolytic safety outcome, and recanalization treatment
Day 90: Modified Rankin Scale, Barthel Index, and mortality
End of Study: End of study/Termination
Meta-Level Reviews
Adjudication: Post case completion, review and evaluation of each remote consultation on
whether the recommendation for or against thrombolytic therapy was appropriate, given the
information presented at each of 3 levels of adjudication.
Central Read: Post case completion, review and evaluation of each Baseline head CT scan
interpretation on whether there was a CT contraindication to thrombolytic therapy.
Trial Groups
There will be two trial groups in this study. The investigators hypothesized (based upon
sample size calculations) that the correct treatment will be recommended at rates of 80%
(telephone) and 90% (full telemedicine).
Target Population
60 AZ patients will be randomized to either telephone-only or video telemedicine
consultation. Appropriateness of therapeutic decision-making, numbers treated, time to
treatment, and completeness of data collection will be evaluated and compared for each
group.
If the protocol or grant application is investigator-initiated, a 200-word (or less)
abstract of the proposed protocol or grant application must be included (an abstract
included in an NIH or other submission is acceptable). If the protocol is sponsor initiated,
a summary written by the Mayo investigator must be included. Summary should include: 1)
Hypothesis, 2) Basic study plan, 3) Statistical method/rationale, 4) Scientific basis or
justification, 5) Inclusion/exclusion criteria, and 6) Monetary consideration. You may type
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Objectives
1. to determine the impact of a site-independent, remote, telemedicine consultation system
on decision making in the Emergency Department, regarding the decision to treat or not
to treat with thrombolytics;
2. to assess the numbers of patients who receive thrombolytics and the time to treatment
in patients evaluated by telemedicine versus telephone only;
3. to assess the appropriateness of thrombolytic treatment decisions in telemedicine
versus telephone-only consultations; and
4. to assess the completeness of the data collection in telemedicine versus telephone-only
consultations.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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