National Institute on Disability, Independent Living, and Rehabilitation Research
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
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 sessions and ongoing training at home
Have a caregiver who, in the judgment of the research team, is qualified to assist the participant in the safe use of TSS
Able to complete in-person training sessions and return to Craig Hospital for assessments
Experience no complicating physical or cognitive conditions as determined by their physician that would preclude the safe use of electrical stimulation
If using prescribed anti-spasticity medications, must be at a stable dose for at least four weeks prior to starting study procedures
Agrees to comply with investigational devices instructions for use, protocol visits, and return of the device
Able to provide informed consent
You may not be if
Experience unstable chronic cardiac or respiratory complaints
Have a recent history of fracture, contractures, or skin pressure injuries that might interfere with the intervention
Received Botox injections to the UEs, neck, or hands within the last three months
Pregnant, planning to become pregnant, or currently breastfeeding
Have breakdown in skin area that will come into contact with electrodes
Prior nerve or tendon transfer procedure for the UEs
Concurrently are participating in another drug or device trial that may interfere with this study
Have an implanted pacemaker, spinal cord stimulator, ventriculoperitoneal shunt, deep brain stimulator, or intrathecal pump
In the opinion of the investigators, the study is not safe or appropriate for the participant
Clareo Health | Spinal Stimulation for Upper Extremity Recovery in the Home
