Reliability and Validity of the Vicorder Device When Measuring Pulse Wave Velocity Within Chronic Stroke Patients

RecruitingOBSERVATIONAL
Enrollment

20

Participants

Timeline

Start Date

March 1, 2020

Primary Completion Date

June 30, 2024

Study Completion Date

June 30, 2024

Conditions
Stroke
Interventions
DEVICE

Blood pressure and ultrasound assessment

No intervention. Participants will undertake an overnight fast prior to each assessment (only water is allowed to be consumed prior to the assessment). Participants will be asked to visit the lab on four separate occasions; the first two sessions will involve triplicated measures of carotid-femoral PWV (cfPWV), brachial-femoral PWV (bfPWV), brachial-ankle PWV (baPWV), femoral-ankle PWV (faPWV) and TT by the Vicorder in both seated and supine position. The SphygmoCor will also be used to assess cfPWV in both seated and supine. During the third and fourth sessions individuals will be randomised into either a supine or seated position. A 3 lead ECG will be attached and ultrasound video clips will be taken at the carotid, brachial, femoral and posterior tibial artery on both the symptomatic and asymptomatic sides to look at stiffness and blood velocity. Following this, the Vicorder will be used to look at cfPWV, bfPWV, baPWV, faPWV and TT on both sides.

Trial Locations (1)

Unknown

RECRUITING

Physiology Laboratory, Winchester

All Listed Sponsors
lead

University of Winchester

OTHER