About this trial
The study will explore the use of a haptic device for sensory substitution in individuals with a movement disorder that has caused loss of plantar sensation. The haptic device consists of two components. The first element is a flexible insole with embedded pressure-sensing elements that transmit the spatial patterns of applied foot pressure over time. The second element is a haptic receiver with embedded actuators that vibrate or heat up in proportion to the transmitted pressure patterns, thus substituting the patient's lost plantar sensation.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Able to ambulate 10 meters with or without assistance
Able and willing to give written consent and comply with study procedures
Disqualifiers
Unable to give written consent or comply with study procedures
Unable to perceive unsafe levels of heat in relevant areas
Has a motor complete spinal cord injury
Have transfemoral (above knee) amputation
Trial design
Single group
Treatments tested in this trial
Haptic Device
DeviceProvides sensory substitution by mapping pressure from the insole sensor onto a corresponding vibrating and heating patch to be worn where more sensation is present.
Treatment groups
Trial outcomes
Primary outcomes
Pressure data from the insoles
The primary outcome is to use the pressure-sensitive insole to ensure that we can accurately record spatial and temporal pressure data from a wide variety of healthy and non-healthy individuals.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Shirley Ryan AbilityLab
Lead sponsor
Querrey Simpson Institute for Bioelectronics
Collaborator
Northwestern University
Collaborator