Transformation of Paralysis to Stepping

Spinal Cord Injuries Clinical Trial

Official title:

Transformation of Paraplegic Paralysis to Overground Stepping in Humans

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04105114
• Other study ID #: 19.0434
• Secondary ID: 1R01NS102920-01A
• Status: Recruiting
• Phase: Early Phase 1
• Start date: September 30, 2019
• Est. completion date: December 31, 2027

Study information

• Verified date: February 2024
• Source: University of Louisville
• Contact: Andrea Willhite, MS
• Phone: 502-582-8675
• Email: andrea.willhite[@]louisville.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The main goal of the project is to develop multiple noninvasive neuromodulatory strategies to facilitate full weight bearing stepping overground in people with paralysis. We will determine the effectiveness of combining noninvasive spinal cord stimulation and the administration of buspirone (a monoaminergic agonist) in facilitating locomotor activity in a gravity-neutral apparatus, during body weight supported stepping on a treadmill, when stepping overground in an assistive robotic exoskeleton, or during full weight bearing stepping overground in a rolling walker. Our objective is to identify the experimental variables that define the efficacy of these novel neuromodulatory techniques over a 5 year period in 15 participants with severe spinal cord injury who are at least one year post-injury.

Description:

Aim 1: Define the relative effectiveness of transcutaneous electrical stimulation at multiple stimulation spinal sites and oral Buspirone in facilitating nonweight-bearing (gravity neutral device, GND) and weight-bearing (treadmill) stepping in individuals with chronic motor complete paralysis. Aim 1.1: Define the relative effectiveness of transcutaneous electrical stimulation at multiple spinal sites to facilitate non-weight-bearing (GND) and weight-bearing (treadmill) stepping in spinal cord injury subjects. Aim 1.2: Define the relative effectiveness of transcutaneous electrical stimulation at multiple spinal sites plus oral Buspirone to facilitate nonweight-bearing (gravity neutral device, GND) and weight-bearing (treadmill) stepping in spinal cord injury subjects. Aim 2: Determine the relative effectiveness of Ekso-technology combined with transcutaneous electrical stimulation and/or oral Buspirone in lowering the robotic assistance and enhancing the ability to step self-assisted in a rolling walker during over-ground stepping in individuals with a chronic, severe (AIS A/B) spinal injury. Aim 3: Determine the relative effectiveness of Ekso-technology combined with transcutaneous electrical stimulation and/or oral Buspirone in lowering the robotic assistance and enhancing the ability to step self-assisted in a rolling walker during over-ground stepping in individuals with motor incomplete (AIS C) paralysis.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 15
• Est. completion date: December 31, 2027
• Est. primary completion date: August 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Ages 18-65 years old;

2. Stable medical condition;

3. More than 12 month's post injury;

4. Non-progressive spinal cord injury, AIS grade of A, B or C;

5. Neurological level of injury below T1 and above T8;

6. Not taking anti-spasticity medications;

7. Presence of active spinally evoked responses over the lumbo-sacral spinal cord using spinal stimulation;

8. Discontinuation of monoamine oxidase inhibitor (if applicable) for at least 2 weeks prior to initiation of treatment with buspirone.

Exclusion Criteria:

1. Active pressure sores;

2. Unhealed bone fractures;

3. Untreated active urinary tract infections;

4. Peripheral neuropathies;

5. Seizure disorders;

6. Cardiopulmonary disease unrelated to spinal cord injury;

7. Anemia;

8. Painful musculoskeletal dysfunction;

9. Contractures in the lower extremities;

10. Lower extremity hardware implantation;

11. Lower extremity lower motor neuron injury;

12. Previous unhealed lower extremity musculoskeletal injuries or disorders, prior to or in conjunction with spinal cord injury;

13. Ventilator dependency;

14. Pregnancy or nursing;

15. Healing wounds/surgical sites along the spine, levels T9-L5;

16. Anti-spasticity implantable pumps;

17. Clinically significant depression, psychiatric disorders, or ongoing drug abuse;

18. Implantable suprapubic catheters;

19. Individuals who are unable to support themselves and/or have difficulty standing;

20. Individuals with abnormal blood panel results related to hepatic function. Up to 10 ml of venous blood will be obtained for the testing;

21. Individuals with increased Creatinine Clearance (Clcr) levels above the normal range;

22. Individuals who are taking drug(s) that interact(s) with Buspirone (BuSpar): Monoamine oxidase inhibitors (MAOIs) - Selegiline (Emsam), Isocarboxazid (Marplan), Phenelzine (Nardil), and Tranylcypromine (Parnate) /these medications must discontinue for at least 2 weeks prior to initiating treatment with Buspirone/; Selective serotonin reuptake inhibitors (SSRIs) - Nefazodone (Serzone) and Trazodone (Oleptro); the blood thinner - Warfarin (Coumadin); Unti-seizure drugs: Phenytoin (Dilantin) and Carbamazepine (Tegretol); Benzodiazepines - Diazepam (Valium) and Triazolam (Halcion); Muscle relaxant - Cyclobenzaprine (Flexeril); Anti-fungal drugs - Itraconazole (Sporanox, Onmel), Itraconazole (Sporanox), and Ketoconazole (Nizoral); Antibiotics - Erythromycin (E.E.S., E-Mycin, Erythrocin) and Rifampin (Rifadin, Rimactane); Steroids (Prednisone and others); Anti-HIV drug - Ritonavir (Norvir); Anti-hypertensive drugs - Diltiazem (Cardizem) and Verapamil (Calan, Verelan, Covera-HS); Anti-psychotic drug - Haloperidol (Haldol);

23. Uncontrolled autonomic dysreflexia;

24. Osteoporosis.

Related Conditions & MeSH terms

• Paralysis
• Spinal Cord Injuries

Intervention

Drug:
• Buspirone
Oral Buspirone 7.5mg - 10mg daily during the treatment phase.

Device:
• Non-invasive Spinal Cord Stimulation
A non-invasive transcutaneous electrical spinal cord stimulator, which can be used a multiple spinal locations.
• Ekso Bionics Exoskeleton
This robotic exoskeleton is designed to assist people with neurological injuries for balance, standing, and stepping overground.
• Gravity Neutral Device
This device is used to train and assess non-weight bearing stepping movements. When using the device, participants will be lying on their side with their legs suspended off the end of a table supported by small slings that are anchored securely to the apparatus.
• Body Weight Supported Treadmill Training
Participants will be supported by a special harness while they are stepping on a treadmill. Trained technicians or therapists will be assist the trunk and legs during stepping as needed.
• Rolling Walker
A standard rolling walker will be used for balance support and stability during stepping overground.

Locations

Country	Name	City	State
United States	Frazier Rehabilitation and Neuroscience Institute	Louisville	Kentucky

Sponsors (2)

Lead Sponsor	Collaborator
University of Louisville	National Institute of Neurological Disorders and Stroke (NINDS)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Lower Extremity Electromyography, change over time	Assessment of muscle activity, measured by electromyography, while the leg is suspended in a gravity neutral position.	Before and after each study phase, 1 year per group.
Primary	Lower Extremity Kinematics, change over time	Assessment of low extremity 3D position, measured by motion analysis system, while the leg is suspended in a gravity neutral position.	Before and after each study phase, 1 year per group.
Primary	Treadmill Electromyography Assessment, change over time	Muscle activity, measured by electromyography, will be recorded during weight supported stepping on a treadmill.	Before and after each study phase, 1 year per group.
Primary	Spinal Pathway Electrophysiology, change over time	Evoked potentials in the lower extremities will recorded in response to nerve or spinal stimulation.	Before and after each study phase, 1 year per group.
Primary	Voluntary Lower Extremity Angles, change over time	Assessments of knee, ankle, and toe movements will be performed by measuring angles produced during flexion and extension. The same units of measure will be used for each part of the leg.	Before and after each study phase, 1 year per group.
Primary	Voluntary Lower Extremity Forces, change over time	Assessments of knee, ankle, and toe forces during movements will be performed by measuring forces produced during flexion and extension. The same units of measure will be used for each part of the leg.	Before and after each study phase, 1 year per group.
Primary	Body Temperature, change over time	We will measure body temperature using standard methods to assess values at rest and during exercise.	Before and after each study phase, 1 year per group.
Primary	Blood Pressure, change over time	We will measure blood pressure (systolic and diastolic) using standard methods to assess values at rest and during exercise.	Before and after each study phase, 1 year per group.
Primary	Heart Rate, change over time	We will measure the heart rate using standard electrocardiography to assess values at rest and during exercise.	Before and after each study phase, 1 year per group.
Primary	Respiration Rate, change over time	We will measure respiratory rate using standard methods to assess values at rest and during exercise.	Before and after each study phase, 1 year per group.
Primary	Dual-energy X-ray absorptiometry, change over time	We will use dual-energy X-ray absorptiometry to measure bone and soft tissue density.	Before and after each study phase, 1 year per group.
Primary	Acoustic Gastro-Intestinal Surveillance, change over time	We will use non-invasive sensors placed on the abdomen to detect signals related to the digestive state.	Before and after each study phase, 1 year per group.
Primary	Bladder capacity, change over time	We will use a standard technique to measure bladder volume change during voiding.	Before and after each study phase, 1 year per group.
Primary	Urodynamics, change over time	We will use a standard technique to measure the abdominal pressure change during voiding.	Before and after each study phase, 1 year per group.
Primary	Cognitive interference, change over time	A cognitive assessment using Stroop test will be administered to assess cognitive function during stress.	Before and after each study phase, 1 year per group.
Primary	Assessment of verbal fluency, change over time	Controlled Oral Word Association Test (COWAT) will be administered to assess verbal fluency that measures ability of spontaneous production of words.	Before and after each study phase, 1 year per group.
Secondary	International Standards of Neurological Classification of Spinal Cord Injury, change over time	This standard clinical assessment assess the level and severity of a spinal cord injury.; The neurological level of injury is rated from A-E. "A" is a motor and sensory complete injury. "E" is completely normal at each spinal segment.; Sensory function is rated as 0-2, or Not Testable. Motor function is rated as 0-5 or Not Testable.	Before and after each study phase, 1 year per group.
Secondary	Spinal Cord Injury Functional Ambulation Inventory, change over time	This 3-part scale measures gait parameters, use of assistive devices, and distances traveled during walking. The gait parameters are scored on a 20-point scale, the assistive device use on a 14-point scale, and the walking distance on a 5-point scale.	Before and after each study phase, 1 year per group.
Secondary	Spinal Cord Independence Measure III, change over time	This 3-part scale is scored out of 100 points possible. The first part (self-care) is scored out of 20. The second part (respiration and sphincter management) is scored out of 40. And the last part (mobility) is scored out of 40.	Before and after each study phase, 1 year per group.
Secondary	Walking Index for Spinal Cord Injury-II, change over time	This is a 20-point scale used to assess the amount of physical assistance needed during walking.	Before and after each study phase, 1 year per group.
Secondary	Ashworth Scale, change over time	This is a 6-part scale to measure and quantify the amount of muscle tone experienced when a joint is moved through a full range of motion.	Before and after each study phase, 1 year per group.