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PubMed
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Stroke Interventions in Clinical Trials
Printable Version
STRokE DOC-LTO
Stroke Team Remote Evaluation Using a Digital Observation Camera- Long Term Outcomes



Principal Investigator
Brett C. Meyer, MD

PI Address
UCSD
San Diego, California,
United States, 92103
Phone: 619-543-7760

Contact Email
bcmeyer@ucsd.edu

Sponsor



Study Size Planned:234
Max Time from onset:12 Months
Min Age:18
Follow-up Duration:12 Months
ISRCTN#NCT00936455
Status:
This study is currently recruiting participants.

Purpose:
To evaluate the long term outcomes of patients previously enrolled in the STRokE DOC telemedicine clinical trial.

Location(s):
California


Design:
Observational, Cohort, Retrospective

Inclusion Criteria
Prior enrollment into the STRokE DOC clinical research trial.

Exclusion Criteria
Patients not previously enrolled into the STRokE DOC clinical research trial.

Patient Involvement:
Patients will participate in data collection assessing long term patient outcomes of patients previously enrolled in a telemedicine vs. telephone clinical trial (STRokE DOC Trial; now completed).

Primary Outcome:
Functional Outcome (mRS) at 6 months after index event;
Functional Outcome (mRS) at 12 months after index event; Functional Outcome (mRS) at current time of contact.

Secondary Outcome:
Recurrent stroke at 6 months after index event; Recurrent stroke at 12 months after index event; recurrent stroke by time of contact; ICH by 6 months; ICH by 12 months; ICH by time of contact.

Comments:
Scientific Name: An Observational Study to Evaluate the Long Term Outcomes of Patients Previously Enrolled in the STRokE DOC Telemedicine Clinical Trial.

Source of Information:
ClinicalTrials.gov

Web Links and Publications:
Efficacy of site-independent telemedicine in the STRokE DOC trial: a randomised, blinded, prospective study.
Lancet Neurol 2008 Sep;7(9):787-95

STRokE DOC
Stroke Trials Registry

STRokE DOC-LTO
ClinicalTrials.gov

This information last updated on: 6/23/2010

Reviewed on: 06/23/2010.

UID: 1093

   

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