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Somatosensation Device Trial

Testing of the Somatosensation Device (SD) for Device Effectiveness While Enhancing Feedback in Lower Extremities

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06168396
Enrollment
12
Registered
2023-12-13
Start date
2024-03-01
Completion date
2024-05-01
Last updated
2024-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Amputation, Neuropathy

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.

Interventions

DEVICESomatosensation Device

The somatosensation device will be worn on the lower limb (either the residual limb for an amputee, or limb with decreased sensation for a participant with diabetic neuropathy) while performing outcome measures.

OTHERBaseline

Participants will perform outcome measures without wearing the somatosensation device.

Sponsors

Shirley Ryan AbilityLab
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 89 Years
Healthy volunteers
No

Inclusion criteria

* 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.

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
Functional Gait Assessment (FGA)Baseline, during the interventionThe 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

MeasureTime frameDescription
10 Meter Walk TestBaseline, during the interventionThe 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.
Mini-BESTestBaseline, during the interventionA multi-task balance assessment that identifies postural control problems across a wide variety of situations.
Activities Specific Balance Confidence Scale (ABC)Baseline, during the interventionA 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.
Vestibular Disorders Activities of Daily Living Scale (VADL)Baseline, during the interventionA 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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026