Peripheral Artery Disease Clinical Trial
Official title:
Project VOICE: Vascular Outcomes Improvement Through Collection of PatiEnt Reported Data
The purpose of this study is to evaluate the feasibility of a digital health platform coupled with walking activity tracking for patients with Peripheral Artery Disease (PAD) and symptoms limited to claudication.
This is a two center, non-blinded, 2 period randomized crossover trial. 50 patient subjects
are planned. Patient participants will be identified and recruited from clinical environments
(including clinics and diagnostic testing departments) at participating sites. Diagnosis and
testing will occur through usual clinical care, and participants will not incur financial
costs related to participation. A crossover design will be utilized, where all participants
will use the VOICE platform with activity tracking for 35 days and usual care for 30 days.
Randomization will determine the order in which participation in the VOICE phase versus the
usual care phase occur. Randomization will occur using a closed envelope system. For patients
in the VOICE platform group, data collection will occur over a total of 35 days, including an
initial 5-day "run in" period during which participants will orient themselves to the system.
Each provider participant will receive a single end-user survey evaluating VOICE from their
perspective.
Screening of patients electronic medical records will be done to determine subject
eligibility. Subjects who meet all inclusion criteria will be approached to participate.
Total duration of subject participation will be 9 weeks during the control and intervention
phases, with a final follow-up survey at 6 months post-enrollment.
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