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Seated Ankle Robot for Foot Drop in Aging and Disabled Populations: A Demonstration Project

Seated Ankle Robot for Foot Drop in Aging and Disabled Populations: A Demonstration Project

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03530592
Enrollment
100
Registered
2018-05-21
Start date
2018-06-01
Completion date
2028-12-31
Last updated
2018-05-21

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

Conditions

Foot Drop, Gait Disorders, Neurologic, Mobility Limitation, Peripheral Nervous System Diseases

Brief summary

The purpose of this research study is to test the utility of an ankle robot in people with ankle weakness and foot drop from a peripheral nervous system injury due to neuromuscular or orthopedic injury.

Detailed description

Many individuals with central nervous system (CNS) injuries (e.g., a stroke) or peripheral nervous system (PNS) injuries (e.g., peroneal nerve injury, neuropathy, radiculopathy, and/or musculoskeletal injury) that affect their ankle movement have residual impairments that affect their walking and balance. These impairments include the disability foot drop, which increases the risk for falling. This study will focus on PNS injuries that cause foot drop. Current therapy to address foot drop is limited primarily to the use of ankle foot orthoses (braces) that help keep the foot from hitting the ground to prevent falling. Also, some individuals with foot drop use functional electrical stimulation to the leg nerve to lift the foot. Regardless, none of these, or other existing, methods to address foot drop cures or even improves significantly the underlying neurological deficit behind this disability. Braces improve walking safety only while they are worn, and functional electrical stimulation does not work when it is turned off, or when the nerve has been severely damaged. Thus, the increased fall risk due to foot drop is generally considered life-long and incurable. The investigators have developed a shoe-interfaced ankle robot with an adaptive control system, to assist an individual with ankle movement only as needed. Data from the investigators' previous studies on foot drop due to stroke show great promise for this ankle robot as a new rehabilitation tool for invididuals with foot drop. The investigators would like to utilize our findings from these stroke studies in learning how they can be used for PNS-related foot drop.

Interventions

DEVICESeated Ankle Robot Training

This intervention employs the use of an adaptive ankle robot control system over a 6-week intervention period.

Sponsors

Baltimore VA Medical Center
Lead SponsorFED

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Seated Ankle Robot Taining

Eligibility

Sex/Gender
ALL
Age
18 Years to 88 Years
Healthy volunteers
No

Inclusion criteria

1. Men and women, aged 18 to 88 years 2. Chronic foot drop and ankle weakness in one leg from a peripheral nervous system injury due to a neuromuscular or orthopedic injury 3. Ability to walk 10 meters and arise from a chair with no human assistance (but usage of usual assistive device\[s\] is permitted)

Exclusion criteria

1. Medical history that would preclude participation in low-intensity seated robotic-assisted rehabilitation 2. Current participation in orthopedic or rehabilitation medical programs 3. Active deep venous thrombosis 4. Distal paretic leg skin lesions, infections, or soft tissue inflammation

Design outcomes

Primary

MeasureTime frameDescription
Ankle dorsiflexion-plantarflexion range of motionChange from baseline to: post-6 weeks of training, and 6 weeks after completion of trainingdegrees
Ankle inversion-eversion range of motionChange from baseline to: post-6 weeks of training, and 6 weeks after completion of trainingdegrees
Gait velocity during self-selected overground walkingChange from baseline to: post-6 weeks of training, and 6 weeks after completion of trainingcm/sec
Postural sway areas during quiet standingChange from baseline to: post-6 weeks of training, and 6 weeks after completion of trainingcm\^2; extent of postural deviations to assess static postural control
Ratio of asymmetric loading in quiet standingChange from baseline to: post-6 weeks of training, and 6 weeks after completion of trainingratio of Newtons of force per leg while standing quietly
Push-off forces during gait initiationChange from baseline to: post-6 weeks of training, and 6 weeks after completion of trainingNewtons; magnitude of forward ground reaction forces.

Countries

United States

Contacts

Primary ContactKate C. Flores
kate.flores@va.gov(410) 637-3242

Outcome results

None listed

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