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.
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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

Candy Tefertiller, PT, DPT, PhD, NCS

303-789-8000

ctefertiller@craighospital.org

CONTACT

Bria Mellick, MS

303-789-8757

bmellick@craighospital.org

CONTACT