Hand and Arm Motor Recovery Via Non-invasive Electrical Spinal Cord Stimulation After Stroke

Stroke, Ischemic Clinical Trial

— HARNESS  

Official title:

Hand and Arm Motor Recovery Via Non-invasive Electrical Spinal Cord Stimulation After Stroke

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05591196
• Other study ID #: STUDY00015990
• Status: Recruiting
• Phase: N/A
• Start date: October 1, 2022
• Est. completion date: December 31, 2024

Study information

• Verified date: December 2023
• Source: University of Washington
• Contact: Fatma Inanici
• Phone: 206-787-2692
• Email: finanici[@]uw.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The recovery from a stroke is often incomplete. It is the leading cause of acquired permanent disability in the adult population. Persistent functional loss of the hand and arm contributes significantly to disability. However, the current standard of care to treat hand and arm movements are inadequate. There is an urgent need for innovative and effective therapies for recovery of the upper limb after stroke. Growing evidence shows that electrical spinal cord stimulation, combined with activity-dependent rehabilitation, enables voluntary movement of paralyzed muscles in some neurologic disorders, such as spinal cord injury. The investigators hypothesize that spinal networks that lost control after stroke can be activated by non-invasive electrical stimulation of the spinal cord to improve functional recovery. The aims of the study are: 1. to determine the improvements in hand and arm function that result from the combined application of non-invasive spinal stimulation and activity-based rehabilitation. Surface electrodes placed over the skin of the neck will be used for non-invasive electrical stimulation of the spinal cord. Functional task practice will be used for activity-dependent rehabilitation, 2. to evaluate long-lasting benefits to hand and arm function that persist beyond the period of spinal stimulation.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 6
• Est. completion date: December 31, 2024
• Est. primary completion date: September 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years to 80 Years

Eligibility

Inclusion Criteria:

• Radiologically documented single ischemic stroke resulted in hemiplegia/hemiparesis
• At least six months post-stroke
• Upper Extremity Fugl-Meyer Assessment score "moderate" or "moderate-mild" (29-53 inclusive out of 66) at the screening visit
• Medically and neurologically stable, as determined by medical history and documented physical examination
• For women of childbearing potential, a negative over-the-counter pregnancy test at study entry and willingness to practice adequate contraception during the study
• Ability to attend sessions three times per week
• Adequate social support to participate in all intervention and baseline, follow-up assessment sessions throughout eight months.
• Ability to read, comprehend and speak English

Exclusion Criteria:

• Hemorrhagic stroke
• History of multiple strokes
• Active implanted stimulator (e.g., pacemaker, vagus nerve stimulator, cochlear implant, etc.) or baclofen pump
• Aphasia or any other deficit in communication that interferes with reasonable study participation
• Moderate to severe cognitive impairment
• Presence of neglect (inability to perceive or awareness of, or loss of attention to the weaker half of the body)
• Severe spasticity in the upper limb
• Taking baclofen more than 30 mg/day
• Change in baclofen dose within four weeks before enrollment
• Receiving benzodiazepines, dantrolene, tizanidine, anticoagulant, or antiepileptic medication
• Botulinum toxin injection to the upper limb muscles within six months before enrollment
• Severe joint contractures in the affected hand and arm
• History of spontaneous seizure that had occurred one month or longer after the stroke

Related Conditions & MeSH terms

• Chronic Stroke
• Ischemic Stroke
• Stroke
• Stroke, Ischemic

Intervention

Device:
• Non-invasive Electrical Spinal Cord Stimulation
Electrical stimulation of the spinal cord using surface electrodes

Other:
• Activity Based Rehabilitation
Exercise therapy targeting paralyzed hand and arm

Locations

Country	Name	City	State
United States	University of Washington	Seattle	Washington

Sponsors (1)

Lead Sponsor	Collaborator
University of Washington

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change from baseline - Fugl-Meyer assessment of the upper limb	The clinician-administered a stroke-specific, performance-based impairment scale. It assesses movement function, sensation, joint range of motion, and pain. The score ranges from 0 to 66. Higher scores indicate better outcomes.	"Measurements at baseline and repeated measurements once every two weeks throughout the study, an average of 8 months."
Primary	Change from baseline - Pinch and grip force	Measurement of hand strengths using a dynamometry.	"Measurements at baseline and repeated measurements once every two weeks throughout the study, an average of 8 months."
Primary	Change from baseline - Modified Ashworth Scale	Clinician-administered test for resistance of a joint to passive movement. This scale grades muscle tone/spasticity. The score ranges from 0 to 4. Higher scores indicate worse outcomes.	"Measurements at baseline and repeated measurements once every two weeks throughout the study, an average of 8 months."
Primary	Change from baseline - Wolf Motor Function Test	Quantifies upper limb motor ability through timed and functional tasks. The score range is 0-75; higher scores denote better function.	"Measurements at baseline and repeated measurements once every two weeks throughout the study, an average of 8 months."
Secondary	Change from baseline - Action Research Arm Test	Clinician-administered observational measure to assess upper extremity performance, such as coordination, dexterity, and functioning, in stroke recovery.	"Measurements at baseline and repeated measurements once every two weeks throughout the study, an average of 8 months."
Secondary	Change from baseline - Box and Blocks Test	Participants move, one by one, the maximum number of blocks from one compartment of a box to another of equal size within 60 seconds. Measures gross manual dexterity.	"Measurements at baseline and repeated measurements once every two weeks throughout the study, an average of 8 months."
Secondary	Change from baseline - Revised Nottingham Sensory Assessment	A standardized scale for assessing sensory impairment in stroke patients. Tactile sensation, proprioception, stereognosis, and two-point discrimination are evaluated.	"Repeated measurements once at baseline, once at the end of each treatment arm and through study completion, an average of 8 months."
Secondary	Change from baseline - Stroke Impact Scale	A self-report questionnaire that evaluates disability and health-related quality of life after stroke. The questionnaire consists of 8 domains: strength, memory and thinking, emotion, communication, activities of daily living, mobility, hand function, and participation/role function. The score ranges from 0 to 100. Higher scores indicate better outcomes.	"Repeated measurements once at baseline, once at the end of each treatment arm and through study completion, an average of 8 months."
Secondary	Change from baseline - Short Form-36	A self-report health survey questionnaire. The score range from 0 to 100. The higher the score, the better the outcome.	"Repeated measurements once at baseline, once at the end of each treatment arm and through study completion, an average of 8 months."
Secondary	Change from baseline - Patients Global Impression of Change	A self-report measure that reflects the participant's belief about the efficacy of treatment: the participant chooses the level of improvement and their functional status between much worse, worse, no change, improved and much improved, compared to the baseline.	"Repeated measurements once at baseline, once at the end of each treatment arm and through study completion, an average of 8 months."
Secondary	Change from baseline - H-reflex test	Electrophysiologic evaluation of the reflex response triggered on the motor nerves when sensory fibers in the peripheral nerve are stimulated.	"Repeated measurements once at baseline, once at the end of each treatment arm and through study completion, an average of 8 months."
Secondary	Change from baseline - Somatosensory evoked potentials test	Electrophysiologic evaluation of sensory pathways between the brain and the limb.	"Repeated measurements once at baseline, once at the end of each treatment arm and through study completion, an average of 8 months."
Secondary	Change from baseline - Spinally evoked motor potentials test	Electrophysiologic evaluation of motor pathways between the central nervous system and the muscles.	"Repeated measurements once at baseline, once at the end of each treatment arm and through study completion, an average of 8 months."