Spinal Stimulation for Upper Extremity Recovery in the Home
Recruiting
N/A
Interventional Study
Cervical Spinal Cord Injury
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 46 (estimated)
- Sponsor
- Craig Hospital · Other
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About This Trial
The purpose of this research is to evaluate the safety, feasibility, and tolerability of non-invasive spinal stimulation used in the home and/or community in combination with a functional home exercise program for the upper extremities (arm/hand function) as well as their combined impacts on changes in upper extremity function. The expected duration of participation in this study is about 31-33 ho…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age 18 or older
* History of traumatic SCI
* Less than 12 months post SCI
* SCI injury level C1-C8
* SCI categorized as AIS B-D
* Have passive range of motion (ROM) within functional limits at wrists, shoulders, and elbows
* Have caregiver support to attend three in-person ses…
Contacts