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Improving Ambulatory Community Access After Paralysis

Improving Ambulatory Community Access After Paralysis

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01570816
Enrollment
6
Registered
2012-04-04
Start date
2012-04-30
Completion date
2021-07-31
Last updated
2018-03-14

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

Conditions

Partial Paralysis, Quadriplegia, Spinal Cord Injury, Stroke, Tetraplegia

Keywords

stroke, partial paralysis, gait correction, functional electrical stimulation, paraplegia, tetraplegia, spinal cord injury

Brief summary

The purpose of this research study is to evaluate the effectiveness of functional electrical stimulation (FES) provided by an implanted pulse generator (IPG) in correcting hip, knee and ankle function to improve walking in people with partial paralysis.

Detailed description

In a surgical procedure electrodes are inserted into muscles of the lower extremities to correct hip, knee and ankle function. The electrode leads are connected to an implanted pulse generator located in the abdomen. After a typical post-operative period of two to five days, the recipient will be discharged home for two to six weeks of moderate activity. Following a 6 week period of laboratory exercise and training, functional use of the neuroprosthesis will begin at home and in the community with follow-up evaluations at 1, 3, 6 and 12 months. Laboratory assessments include walking speed and distance, physiologic cost, muscle strength, measure of spasticity, and gait analysis with and without stimulation. A number of self-reporting instruments are administered to capture individual's participation, quality of life and various aspects of perceived community ambulation.

Interventions

DEVICEIRS-8 (8 channel implanted receiver stimulator)

Surgical implantation of an 8 channel pulse generator to stimulate paralyzed muscles of the lower extremities

Sponsors

Louis Stokes VA Medical Center
Lead SponsorFED

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* problems walking because of paralysis for more than 6 months * weak hip flexors and extensors or excessive tone * weak ankle dorsiflexors (muscles bringing the foot up) * weak plantar flexors (ankle muscles for push-off) * foot drop that is causing dragging or catching toes during walking * swinging the leg sideways or hiking the hip to clear affected leg during stepping * endurance to walk at least 10 ft with minimal assistance * hip extension range to neutral * hip flexion range greater or equal to 90 degrees * ankle range to neutral * sufficient upper extremity function to use a walking aid * muscles respond to electrical stimulation

Exclusion criteria

* cardiac arrythmias * demand pacemaker * pregnancy * Parkinson's disease * traumatic brain injury * autoimmune deficiency * uncontrolled diabetes * significant edema of the affected limb * active pressure ulcers or open wounds * sepsis or an active infection * severe osteoporosis * uncontrolled seizures * moderate depression

Design outcomes

Primary

MeasureTime frameDescription
The effect of functional electrical stimulation of the hip, knee and ankle muscles to improve walking in people with partial paralysisup to 36 monthsExperiments involving analyses of individual's speed, distance and quality of walking will be performed both with and without stimulation to determine if individuals are able to improve community ambulatory access with use of neuroprosthesis.

Secondary

MeasureTime frameDescription
Feasibility of initiating a step with a trigger from an accelerometer incorporated in the external control unit to adjust to environmental circumstances and situations encountered in community ambulationup to 36 monthsExperiments involving analyses of individual's speed, distance and quality of walking will be performed both with and without accelerometer triggered stepping to determine if individuals are able to adjust to environmental circumstances and situations encountered in community ambulation.

Countries

United States

Contacts

Primary ContactLisa M Lombardo, MPT
llombardo@fescenter.org216-791-3800

Outcome results

None listed

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