The purpose of this study is to investigate the accuracy of a Smart Foot Mat for signals associated with diabetic foot ulcers in high-risk patients.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
132
Phoenix VA Health Care System
Phoenix, Arizona, United States
University of Arizona
Tucson, Arizona, United States
Center for Clinical Research Castro Valley
Castro Valley, California, United States
Limb Preservation Platform
Fresno, California, United States
Occurrence of Plantar Diabetic Foot Ulcer
Time frame: Through study completion or subject withdrawal (34 weeks per-protocol)
Subject Adherence in Daily Use of the Study Device
Time frame: Through study completion or subject withdrawal (34 weeks per-protocol)
Device-related Trips/Falls
Time frame: Through study completion or subject withdrawal (34 weeks per-protocol)
Device-related Injuries
Time frame: Through study completion or subject withdrawal (34 weeks per-protocol)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
VA Long Beach Health System
Long Beach, California, United States
Miami VA Healthcare System
Miami, Florida, United States
MetroWest Medical Center
Framingham, Massachusetts, United States
Greenville Health System
Greenville, South Carolina, United States