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NCT05191121

Improving Upper Extremity Function and Trunk Stability After Cervical Spinal Cord Injury (SCI)

Enrolling by Invitation
NAAges 18+InterventionalTreatment
Craig Hospital
~99 participants
Updated 2026-03-30 on ClinicalTrials.gov
What's tested:FTP AloneFTP+Con-FESFTP+WPHF-FES

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Capabilities of Upper Extremity Test (CUE-T)
Measured over Week 0 to Week 12

Conditions

Cervical Spinal Cord Injury

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Cervical spinal cord injury

NCT05191121

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Craig Hospital

    Englewood, Coloradono site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Want this trial checked against your situation?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

History of traumatic SCI
Less than 5months post SCI
SCI injury level C1-C8
SCI categorized as AIS B-D
Currently receiving inpatient rehabilitation at Craig Hospital
Passive range of motion (ROM) within functional limits at wrists, shoulders, and elbows
Demonstrate motor response to electrical stimulation in majority of UE muscle groups below level of injury (tested during screening)
No complicating physical or cognitive conditions (as determined by their physician) that would preclude safe use of electrical stimulation
Able to complete study as an outpatient if discharged from inpatient rehabilitation before completing 40 sessions of training

Exclusion

Unstable chronic cardiac or respiratory complaints
Current or history of UE contracture or skin pressure injuries that might interfere with intervention
Received Botox injections within the last 3 months
Pregnant
Implanted devices including: pacemaker, spinal cord stimulator, ventriculoperitoneal shunt, deep brain stimulator, or intra-thecal pump.

What this trial measures

  • Capabilities of Upper Extremity Test (CUE-T)Week 0 to Week 12

    32 item test, each item scored on a 0-4 point scale with total scores ranging from 0-128.