Restorative Neuromodulation for Lower Extremity Functions
NCT ID: NCT04171375
Last Updated: 2022-01-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
2 participants
INTERVENTIONAL
2019-04-01
2021-11-30
Brief Summary
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Detailed Description
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Traumatic injury to the central nervous system (CNS) such as SCI is devastating events leaving patients with impairment of motor, sensory and autonomic functions. Mainstay for the treatment is still limited to rehabilitation by physical therapy and training. In few patients, however, neuroplasticity and repair mechanisms are considered to contribute to recovery of paresis in the acute stage of the injury and stops in the chronic stage. But, recent groundbreaking studies have shown that the recovery can be further amplified in the chronic stage by the novel treatment of trans-spinal electrical stimulation. However, the rehabilitation related to this recovery is not very significant, and thus it is a challenge to be convinced with the efficacy of this new therapy. A combination therapy of trans-spinal electrical stimulation along with body-weight would promote better recovery and benefit the patients more. The current study will further assist the researchers to design such combinational therapeutic intervention for neurologically impaired patients to stimulate to walk again. Successful translation of this novel technology would facilitate the paraplegic community to become more healthy, independent and happy.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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trans-spinal Electrical Stimulation (tsES)
trans-spinal Electrical Stimulation (tsES)
The trans-spinal pulsed-current stimulation utilizes non-invasive russian stimulation using a research grade stimulator and direct-current stimulation utilizes non-invasive constant stimulation using a medical grade stimulator. Both pulsed- and direct-current stimulation will be achieved with cutaneous cathode electrodes attached to the dorsal aspect of the back overlying at and bellow thoracic vertebrae and anode electrodes placed over the iliac crests or lower abdomen. Spinal motor evoked potentials will be induced by trans-spinal pulsed-current stimulation (parameters, 1 Hz with a 1 millisecond pulse width and monophasic waveform) to determine recruitment profiles of proximal and distal motor pools with increasing stimulation intensity ranging from 10-200 milliampere. Stimulation parameters for the therapeutic stimulation will be ranged from 5-50 Hz and 20-200 milliampere. For direct-current stimulation, the stimulation current will be kept constant at 2-2.5 milliampere.
Interventions
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trans-spinal Electrical Stimulation (tsES)
The trans-spinal pulsed-current stimulation utilizes non-invasive russian stimulation using a research grade stimulator and direct-current stimulation utilizes non-invasive constant stimulation using a medical grade stimulator. Both pulsed- and direct-current stimulation will be achieved with cutaneous cathode electrodes attached to the dorsal aspect of the back overlying at and bellow thoracic vertebrae and anode electrodes placed over the iliac crests or lower abdomen. Spinal motor evoked potentials will be induced by trans-spinal pulsed-current stimulation (parameters, 1 Hz with a 1 millisecond pulse width and monophasic waveform) to determine recruitment profiles of proximal and distal motor pools with increasing stimulation intensity ranging from 10-200 milliampere. Stimulation parameters for the therapeutic stimulation will be ranged from 5-50 Hz and 20-200 milliampere. For direct-current stimulation, the stimulation current will be kept constant at 2-2.5 milliampere.
Eligibility Criteria
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Inclusion Criteria
* Lower-extremity paralyzed and half of key muscles below neurological level having a motor score of less than 2/5
* Female subjects must be on standard contraception method and must not be pregnant throughout the study
* Segmental reflexes are functional below the lesion
* Ability to exercises 1-2 hours per day and commit for 1 year training program
Exclusion Criteria
* Received of Botox injections in the prior 6 months
* Weakened bone, unhealed fracture, contracture, pressure sore, or infection that might interfere with the exercise
* Thoracic or lumbar fusion with any metal which may interfere with electric currents
* Other electronic implants such as cardiac pacemaker, defibrillator, shunt, stent etc.
* Currently receiving treatments for pain management or spasticity or depression.
19 Years
55 Years
ALL
Yes
Sponsors
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University of California, Los Angeles
OTHER
Hospital Authority, Hong Kong
OTHER_GOV
The Hong Kong Polytechnic University
OTHER
Responsible Party
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Dr Monzurul Alam
Research Assistant Professor
Principal Investigators
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Monzurul Alam, PhD
Role: PRINCIPAL_INVESTIGATOR
Research Assistant Professor
Locations
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Department of Biomedical Engineering, The Hong Kong Polytechnic University
Kowloon, , Hong Kong
Countries
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Other Identifiers
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HSEARS20190201002
Identifier Type: -
Identifier Source: org_study_id
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