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taVNS for Upper Limb Rehabilitation

Medical University of South Carolina (MUSC) logo

Medical University of South Carolina (MUSC)

Status and phase

Completed
Early Phase 1

Conditions

Stroke

Treatments

Device: Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) + Task Specifc Training

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04129242
5P20GM109040 (U.S. NIH Grant/Contract)
00086291

Details and patient eligibility

About

This study explores the use of a new form of neuromodulation known as transcutaneous auricular vagus nerve stimulation (taVNS) which stimulates the ear. This stimulation will be delivered concurrently with upper limb motor rehabilitation training (3 days/week for 4 weeks) in chronic stroke patients. Patients will undergo a series of baseline assessments (including a brain scan), a 4-week course of motor rehabilitation, and post-assessments (including a second brain scan)

Full description

This study aims to refine and develop closed loop taVNS, establish activity with key biomarkers, and show initial feasibility in a small clinical trial. For paired taVNS to succeed as a clinical treatment, it is critical to develop and refine a closed-loop taVNS platform that delivers stimulation concurrently during specific movements of the motor rehabilitation training.

Aim 1 develops this novel motion-gated closed-loop system that delivers taVNS in synchrony with specific upper limb motor activation (n=5) Aim 2 will combine the development of the closed-loop system with the investigator's mechanistic understanding to explore an open-label pilot trial (n=20) using closed-loop taVNS paired with task-specific training to determine the feasibility, safety, and potential effect size of this novel combination therapy.

Enrollment

20 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-80 years old
  • Ischemic or hemorrhagic stroke that occurred at least 6 months prior
  • Completed conventional rehabilitation therapy at least one month prior
  • Unilateral limb weakness with Fugl Meyer-Upper Extremity Scale score less than or equal to 58 (out of 66)

Exclusion criteria

  • Primary intracerebral hematoma, or subarachnoid hemorrhage
  • Bilateral upper extremity weakness
  • Other concomitant neurological disorders affecting upper extremity motor function
  • Documented history of dementia before or after stroke
  • Documented history of uncontrolled depression or psychiatric disorder either before or after stroke which could affect their ability to participate in the experiment
  • Uncontrolled hypertension despite treatment, specifically SBP (Systolic Blood Pressure) / DBP (Diastolic Blood Pressure) >=180/100mmHg at baseline
  • Contraindicated for MRI scanning.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

20 participants in 2 patient groups

"paired" taVNS + Task Specific Training
Active Comparator group
Treatment:
Device: Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) + Task Specifc Training
"unpaired" taVNS + Task Specific Training
Active Comparator group
Treatment:
Device: Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) + Task Specifc Training

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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