Study Summary
This trial looks at whether the MyoPro device can help improve upper extremity function in people with incomplete spinal cord injury.
Eligible Conditions
- Spinal Cord Injury
Treatment Effectiveness
Effectiveness Progress
Study Objectives
6 Primary · 0 Secondary · Reporting Duration: Approximately 10 weeks
Approximately 10 weeks
Brain signals measurement
CUE-Q
GRASSP
Muscle strength measurement
Range of motion of hands and arms
Spasticity measurement
Trial Safety
Safety Progress
Trial Design
3 Treatment Groups
Myo-SB
1 of 3
Control
1 of 3
MyoPro
1 of 3
Active Control
Experimental Treatment
24 Total Participants · 3 Treatment Groups
Primary Treatment: MyoMo · No Placebo Group · N/A
MyoPro
Device
Experimental Group · 1 Intervention: MyoMo · Intervention Types: DeviceMyo-SB
Other
ActiveComparator Group · 1 Intervention: Myo-SB · Intervention Types: OtherControl
Other
ActiveComparator Group · 1 Intervention: Control · Intervention Types: OtherTrial Logistics
Trial Timeline
Screening: ~3 weeks
Treatment: Varies
Reporting: approximately 10 weeks
Who is running the clinical trial?
United States Department of DefenseFED
779 Previous Clinical Trials
202,395 Total Patients Enrolled
Kessler FoundationLead Sponsor
155 Previous Clinical Trials
10,291 Total Patients Enrolled
Eligibility Criteria
Age 18 - 80 · All Participants · 9 Total Inclusion Criteria
Mark “Yes” if the following statements are true for you:You are able to tolerate functional tasks for 60min with intermittent rests without excessive fatigue.
You are between ages 18-80.
You are medically stable.
You are able to communicate in English with the study staff.
You are taking all prescribed medication as prescribed.
You have some visible muscle contraction (with or without range of motion) on their upper extremity as determined by study staff.
You have full passive range of motion for elbow flexion and extension.
Who else is applying?
What state do they live in?
| New York | 100.0% |
How old are they?
| < 18 | 100.0% |
What site did they apply to?
| Kessler Foundation | 100.0% |
What portion of applicants met pre-screening criteria?
| Met criteria | 100.0% |
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Back to top
Conditions
Cancer Related
Treatments