NCT06543277NARecruiting
Safety and Feasibility of Paired Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) With Upper Limb Rehabilitation in Incomplete Spinal Cord Injury
The University of Texas Health Science Center, Houston
Start Date
8/15/2025
Completion Date
12/30/2027
Summary
The purpose of this study is to evaluate the safety and feasibility of transcutaneous auricular Vagus Nerve Stimulation (taVNS) paired with upper-limb rehabilitation in adults with tetraplegia caused by cervical spinal cord injury.
Eligibility Criteria
Age Range: 18 years to No maximum
Inclusion Criteria:
* diagnosis of traumatic incomplete (AIS B-D) cervical spinal cord injury (C8 and above)
* at least 12 months post-traumatic SCI but less than 10 years post-SCI
* demonstrate some residual movement in the upper limb (e.g., able to perform pinch movement with thumb and index finger sufficient to grip small objects such as marble)
Exclusion Criteria:
* non-traumatic SCI
* recent ear trauma and skin lesions at the site of stimulation, such as sunburn, cuts, and open sores,
* facial or ear pain,
* allergic reaction to adhesives and electrodes,
* any current or past history of cardiovascular disorders,
* intracranial metal implants, pacemakers,
* concomitant clinically significant brain injury,
* receiving medication that may significantly interfere with the actions of VNS on neurotransmitter systems at study entry
* If there is a plan for alteration in upper-extremity therapy or medication for muscle tone during the course of the study;
* medical or mental instability;
* pregnancy or plans to become pregnant during the study period
Interventions
DEVICE
Transcutaneous Auricular Vagus Nerve Stimulation (taVNS)
Conditions
Chronic Incomplete Cervical Spinal Cord Injury (SCI)
Locations
Neurorecovery Research Center, TIRR MHH
Houston, Texas 77030
United States
The University of Texas Health Science Center at Houston
Houston, Texas 77030
United States