Somatosensation Device Trial
- Conditions
- NeuropathyAmputation
- Interventions
- Other: BaselineDevice: Somatosensation Device
- Registration Number
- NCT06168396
- Lead Sponsor
- Shirley Ryan AbilityLab
- Brief Summary
This research is being done to test a new device, called the Somatosensation Device, with people who have either a below knee amputation, or neuropathy (i.e. decreased sensation) in their legs. When people have lost sensation in their feet, it may make walking and balance more difficult. The Somatosensation Device is designed to substitute the loss of feeling in a foot by pressing on nerves on the surface of the leg. It presses on the nerves by using a pneumatic balloon to put pressure on your skin. If people receive this extra sensation feedback, it may help improve their walking and balance.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 12
- Have a below-knee amputation (either unilateral or bilateral) or neuropathy in their lower limbs.
- Ability to wear the somatosensation device on their lower limbs
- Ability to wear test equipment and heart rate monitors.
- Ability to follow simple directions.
- History of severe back pain in the last 3 months.
- History of severe knee pain in the last 3 months.
- Unable to walk for 3 minutes with or without an assistive device
- Poor skin integrity (i.e open wounds, skin breakdown) that could be made worse by wearing the somatosensation device.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Baseline (Without Somatosensation Device) Baseline Participants will perform all outcome measures without wearing the somatosensation device. With Somatosensation Device Somatosensation Device Participants will perform all outcome measures while wearing the somatosensation device.
- Primary Outcome Measures
Name Time Method Functional Gait Assessment (FGA) Baseline, during the intervention The Functional Gait Assessment is a test to assess an individual's postural stability and ability to perform multiple motor tasks while walking. Tests include walking at different speeds, walking with head turns, turns, stepping over obstacles, walking tandem, walking with eyes closed, walking backwards, and stair navigation. Scores are on a 0-30 scale, with higher scores showing better balance and mobility.
- Secondary Outcome Measures
Name Time Method Activities Specific Balance Confidence Scale (ABC) Baseline, during the intervention A self-reported questionnaire that measures a participant's confidence in their balance in performing various activities without falling or becoming unsteady. Scores are on a 0-100% confidence scale, with higher scores equaling greater confidence.
Mini-BESTest Baseline, during the intervention A multi-task balance assessment that identifies postural control problems across a wide variety of situations.
Vestibular Disorders Activities of Daily Living Scale (VADL) Baseline, during the intervention A self-reported questionnaire that evaluates the effects of vertigo and balance disorders on independence routine activities of daily living. Scores range from 1-8, with lower scores indicating greater independence with activities.
10 Meter Walk Test Baseline, during the intervention The 10MWT assesses walking speed in meters per second. In the 10MWT, subjects are directed to walk at their self-selected and maximum safe speed with the effects of acceleration and deceleration minimized (by adding 2 meters at the beginning and at the end of the course to isolate the subject's steady state speed). Any assistive device and orthotic should be kept consistent and documented. Participants will complete three trials at their self-selected speed and three trials at their fast but still safe speed. This will be performed over the GAITRite electronic walkway, to measure temporal-spatial gait parameters.
Trial Locations
- Locations (1)
Shirley Ryan AbilityLab
🇺🇸Chicago, Illinois, United States