search
Back to results

taVNS Paired With Motor Training for Upper-extremity Rehabilitation in Stroke Patients

Primary Purpose

Upper Extremity Dysfunction, Stroke

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
paired taVNS
Unpaired taVNS
Sham taVNS
Sponsored by
Qiuyou Xie
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Upper Extremity Dysfunction focused on measuring Upper Extremity Dysfunction, Ischemic Stroke, Transcutaneous auricular vagus nerve stimulation, Electromyography

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients diagnosed with ischemic stroke according to a clinically qualified physician with reference to the Chinese Stroke Prevention and Control Guideline (2021). Patients in the acute/recovery phase (after 2 weeks of onset) with stable signs; No previous neuropsychiatric-related diseases; No significant impairment of cognitive function and able to cooperate in completing the corresponding rehabilitation training; With unilateral upper limb dysfunction; Patients who have not received various neuromodulation rehabilitation treatments; No contraindications to taVNS; Patients voluntarily cooperated with the study and signed an informed consent form. Exclusion Criteria: Patients have other mental health disorders (dementia, Parkinson's disease, depression, schizophrenia, bipolar disorder, etc.) Patients have uncontrolled epilepsy, i.e., having had a seizure within 4 weeks prior to enrollment Patients have cardiac arrhythmias or other abnormalities Patients have a history of respiratory disease or disorder, including dyspnea and asthma; The presence of gastrointestinal disorders such as diarrhea and vomiting that make it difficult for the patient to cooperate Patients have a history of vasovagal syncope Patients are under treatment with other neurostimulation/modulation The presence of severe spasticity, other serious injuries to the upper extremities, or other medical conditions Patients have difficulty in communication and understanding and inability to cooperate in completing the test; Women who are pregnant or breastfeeding.

Sites / Locations

  • Zhujiang Hospital of Southern Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Sham Comparator

Arm Label

Paired taVNS

Unpaired taVNS

Sham taVNS

Arm Description

Upper extremity motor rehabilitation training will be paired with taVNS.

Unpaired transcutaneous vagus nerve stimulation for upper limb motor rehabilitation will be administered.

Upper limb motor rehabilitation training will be paired with sham-stimulation.

Outcomes

Primary Outcome Measures

Changes from Baseline Fugl-Meyer Assessment of Upper Extremity (FMA-UE) Scores
The Fugl-Meyer Assessment - Upper Extremity (FMA-UE) is a stroke-specific assessment that measures performance at the body function/impairment domain. It uses an ordinal scale for scoring 33 items for the upper limb function with a total possible score of 66. The FMA-UE is one of the most widely used quantitative measures of motor impairment after stroke. Studies have shown excellent inter-rater, and intra-rater reliability, and construct validity of FMA-UE. In addition, empirical evidence suggests that the FMA-UE is responsive to the change in rehabilitation. Higher scores are indicative of better outcomes. The primary outcome measures are as follows: Difference in the changes from baseline FMA-UE scores between paired taVNS and shame taVNS groups. Difference in the changes from baseline FMA-UE scores between unpaired taVNS and shame taVNS groups. Difference in the changes from baseline FMA-UE scores between paired taVNS and unpaired taVNS groups.

Secondary Outcome Measures

Changes from Baseline Wolf motor function test (WMFT)
The Wolf motor function test (WMFT) is a widely used measure for upper extremity motor abilities. It uses a 6-point ordinal scale for scoring 17 items with a total core of 85. Higher scores are indicative of better outcomes. We will compare the differences in the changes from baseline WMFT scores between paired taVNS and shame taVNS groups, between unpaired taVNS and shame taVNS groups, and between paired taVNS and unpaired taVNS groups.
Changes from Baseline Brunnstrom recovery stages (BRS)
The Brunnstrom recovery stages (BRS) is a measure for assessing motor function. The BRS contains 3 items rated on a 6-level Likert-type scale. Higher scores are indicative of better outcomes. We will compare the differences in the changes from baseline BRS scores between paired taVNS and shame taVNS groups, between unpaired taVNS and shame taVNS groups, and between paired taVNS and unpaired taVNS groups.
Changes from Baseline Barthel Index (BI)
The Barthel Index (BI) is a measure of independence in the activities of daily living (ADLs). The BI includes the 10 ADLs with a total score of 100. Higher scores are indicative of better outcomes. We will compare the differences in the changes from baseline BI scores between paired taVNS and shame taVNS groups, between unpaired taVNS and shame taVNS groups, and between paired taVNS and unpaired taVNS groups.
Changes from Baseline Hong Kong version of the Functional Test for the Hemiplegic Upper Extremity (FTHUE-HK)
The Hong Kong version of the Functional Test for the Hemiplegic Upper Extremity (FTHUE-HK) is another measure for ADL. It uses a 7-point ordinal scale for scoring 12 items with a total score of 84. Higher scores are indicative of better outcomes. We will compare the differences in the changes from baseline FTHUE-HK scores between paired taVNS and shame taVNS groups, between unpaired taVNS and shame taVNS groups, and between paired taVNS and unpaired taVNS groups.
Changes from Baseline EMG features
EMG will be acquired from 2 channels on the upper limb. When participants perform motor training, the peak amplitudes and the zero crossing rate of EMG signals at the time domain and the relative spectral power (RSP) of EMG signals at 20 to 200 Hz will be calculated on-line. Difference in the changes from baseline EMG features between paired taVNS and shame taVNS groups. Difference in the changes from baseline EMG features scores between unpaired taVNS and shame taVNS groups. Difference in the changes from baseline EMG features scores between paired taVNS and unpaired taVNS groups.
Changes from Baseline EEG features
EEG will be acquired from 66 channels following the international 10-20 System for 10 mins. The relative spectral power (RSP) of participants will be calculated by the selected artifact-free EEG epochs at five frequency bands: δ (1-4 Hz), θ (4-8 Hz), α (8-13 Hz), β (13-30 Hz), and γ (30-45 Hz). The investigators will perform off-line analysis to calculate RSP. Difference in the changes from baseline EEG features between paired taVNS and shame taVNS groups. Difference in the changes from baseline EEG features scores between unpaired taVNS and shame taVNS groups. Difference in the changes from baseline EEG features scores between paired taVNS and unpaired taVNS groups.

Full Information

First Posted
June 25, 2023
Last Updated
July 4, 2023
Sponsor
Qiuyou Xie
Collaborators
BrainClos Co., LTD.
search

1. Study Identification

Unique Protocol Identification Number
NCT05943431
Brief Title
taVNS Paired With Motor Training for Upper-extremity Rehabilitation in Stroke Patients
Official Title
A Single-center Randomized, Double-blind Controlled Trial Investigating the Efficacy of Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) in Improving Upper Extremity Motor Function in Stroke Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 1, 2023 (Actual)
Primary Completion Date
July 1, 2025 (Anticipated)
Study Completion Date
December 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Qiuyou Xie
Collaborators
BrainClos Co., LTD.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: Recently, there has been increasing attention on the application of transcutaneous auricular vagus nerve stimulation (taVNS) in ischemic stroke. This innovative technique involves non-invasive electrical stimulation of the vagus nerve. A controlled study by Dawson et al. (2021), conducted using a randomized, double-blind approach, has demonstrated that vagus nerve stimulation (VNS) when paired with motor function training, can effectively promote the improvement of motor dysfunction in stroke patients. In the same year, the Food and Drug Administration approved the use of VNS, alongside motor rehabilitation training, for upper extremity dysfunction caused by stroke. However, it is worth noting that VNS requires surgical procedures with contraindications. Consequently, researchers are exploring taVNS as a potential alternative intervention. Compared to VNS, taVNS offers a low-risk and user-friendly intervention that eliminates the need for surgery and the associated postoperative complications. A recent meta-analysis has shown that the efficacy of taVNS in upper extremity rehabilitation for stroke patients can be comparable to that of VNS. Therefore, pairing taVNS with motor training holds promise as a valuable clinical tool for post-stroke rehabilitation. Methods and Design: This study presents a protocol for a single-center randomized, double-blind controlled trial. A total of 150 participants will be enrolled and randomly assigned to one of three groups (Group 1, Group 2, or Group 3) in a 1:1:1 ratio. Each patient will undergo a total of 14 treatment sessions. In Group 1, patients will receive motor training paired with taVNS. In Group 2, patients will receive motor training and taVNS interventions, seperately. In Group 3, patients will receive motor training paired with sham taVNS. Primary and secondary outcome measures will be assessed at baseline and after taVNS treatment. The primary outcome will be determined by evaluating the behavioral response to treatment, using the Fugl-Meyer Assessment of Upper Extremity (FMA-UE). Discussion: This study aims to elucidate the role of paired taVNS in the rehabilitation of upper extremity dysfunction in stroke patients. The researchers propose a novel approach by pairing taVNS with individualized training actions, utilizing electromyography (EMG) during motor training to precisely trigger taVNS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Upper Extremity Dysfunction, Stroke
Keywords
Upper Extremity Dysfunction, Ischemic Stroke, Transcutaneous auricular vagus nerve stimulation, Electromyography

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Paired taVNS
Arm Type
Experimental
Arm Description
Upper extremity motor rehabilitation training will be paired with taVNS.
Arm Title
Unpaired taVNS
Arm Type
Active Comparator
Arm Description
Unpaired transcutaneous vagus nerve stimulation for upper limb motor rehabilitation will be administered.
Arm Title
Sham taVNS
Arm Type
Sham Comparator
Arm Description
Upper limb motor rehabilitation training will be paired with sham-stimulation.
Intervention Type
Device
Intervention Name(s)
paired taVNS
Intervention Description
The stimulator will be placed on the left ear of the patient. While the patient performs the action training, the EMG signal feature evoked by the action will trigger an electrical stimulation of the transcutaneous auricular vagus nerve. The amplitude of the electrical stimulation will be adjusted under the patient's pain threshold. The intervention will be performed daily for 14 days.
Intervention Type
Device
Intervention Name(s)
Unpaired taVNS
Intervention Description
The stimulator will be placed on the patient's left ear. Patients will receive taVNS with pulses every 5-7 seconds. Following the stimulation, motor training will be performed. The motor training will be identical to that of the paired group. The amplitude of the electrical stimulation will be adjusted under the patient's pain threshold. The intervention will be performed daily for 14 days.
Intervention Type
Device
Intervention Name(s)
Sham taVNS
Intervention Description
The stimulator will be placed on the patient's left ear. The amplitude of the electrical stimulation will be adjusted at 0 mA. The intervention will be performed daily for 14 days.
Primary Outcome Measure Information:
Title
Changes from Baseline Fugl-Meyer Assessment of Upper Extremity (FMA-UE) Scores
Description
The Fugl-Meyer Assessment - Upper Extremity (FMA-UE) is a stroke-specific assessment that measures performance at the body function/impairment domain. It uses an ordinal scale for scoring 33 items for the upper limb function with a total possible score of 66. The FMA-UE is one of the most widely used quantitative measures of motor impairment after stroke. Studies have shown excellent inter-rater, and intra-rater reliability, and construct validity of FMA-UE. In addition, empirical evidence suggests that the FMA-UE is responsive to the change in rehabilitation. Higher scores are indicative of better outcomes. The primary outcome measures are as follows: Difference in the changes from baseline FMA-UE scores between paired taVNS and shame taVNS groups. Difference in the changes from baseline FMA-UE scores between unpaired taVNS and shame taVNS groups. Difference in the changes from baseline FMA-UE scores between paired taVNS and unpaired taVNS groups.
Time Frame
Immediately after 14 days' sessions
Secondary Outcome Measure Information:
Title
Changes from Baseline Wolf motor function test (WMFT)
Description
The Wolf motor function test (WMFT) is a widely used measure for upper extremity motor abilities. It uses a 6-point ordinal scale for scoring 17 items with a total core of 85. Higher scores are indicative of better outcomes. We will compare the differences in the changes from baseline WMFT scores between paired taVNS and shame taVNS groups, between unpaired taVNS and shame taVNS groups, and between paired taVNS and unpaired taVNS groups.
Time Frame
Immediately after 14 days' sessions
Title
Changes from Baseline Brunnstrom recovery stages (BRS)
Description
The Brunnstrom recovery stages (BRS) is a measure for assessing motor function. The BRS contains 3 items rated on a 6-level Likert-type scale. Higher scores are indicative of better outcomes. We will compare the differences in the changes from baseline BRS scores between paired taVNS and shame taVNS groups, between unpaired taVNS and shame taVNS groups, and between paired taVNS and unpaired taVNS groups.
Time Frame
Immediately after 14 days' sessions
Title
Changes from Baseline Barthel Index (BI)
Description
The Barthel Index (BI) is a measure of independence in the activities of daily living (ADLs). The BI includes the 10 ADLs with a total score of 100. Higher scores are indicative of better outcomes. We will compare the differences in the changes from baseline BI scores between paired taVNS and shame taVNS groups, between unpaired taVNS and shame taVNS groups, and between paired taVNS and unpaired taVNS groups.
Time Frame
Immediately after 14 days' sessions
Title
Changes from Baseline Hong Kong version of the Functional Test for the Hemiplegic Upper Extremity (FTHUE-HK)
Description
The Hong Kong version of the Functional Test for the Hemiplegic Upper Extremity (FTHUE-HK) is another measure for ADL. It uses a 7-point ordinal scale for scoring 12 items with a total score of 84. Higher scores are indicative of better outcomes. We will compare the differences in the changes from baseline FTHUE-HK scores between paired taVNS and shame taVNS groups, between unpaired taVNS and shame taVNS groups, and between paired taVNS and unpaired taVNS groups.
Time Frame
Immediately after 14 days' sessions
Title
Changes from Baseline EMG features
Description
EMG will be acquired from 2 channels on the upper limb. When participants perform motor training, the peak amplitudes and the zero crossing rate of EMG signals at the time domain and the relative spectral power (RSP) of EMG signals at 20 to 200 Hz will be calculated on-line. Difference in the changes from baseline EMG features between paired taVNS and shame taVNS groups. Difference in the changes from baseline EMG features scores between unpaired taVNS and shame taVNS groups. Difference in the changes from baseline EMG features scores between paired taVNS and unpaired taVNS groups.
Time Frame
Immediately after 14 days' sessions
Title
Changes from Baseline EEG features
Description
EEG will be acquired from 66 channels following the international 10-20 System for 10 mins. The relative spectral power (RSP) of participants will be calculated by the selected artifact-free EEG epochs at five frequency bands: δ (1-4 Hz), θ (4-8 Hz), α (8-13 Hz), β (13-30 Hz), and γ (30-45 Hz). The investigators will perform off-line analysis to calculate RSP. Difference in the changes from baseline EEG features between paired taVNS and shame taVNS groups. Difference in the changes from baseline EEG features scores between unpaired taVNS and shame taVNS groups. Difference in the changes from baseline EEG features scores between paired taVNS and unpaired taVNS groups.
Time Frame
Immediately after 14 days' sessions

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients diagnosed with ischemic stroke according to a clinically qualified physician with reference to the Chinese Stroke Prevention and Control Guideline (2021). Patients in the acute/recovery phase (after 2 weeks of onset) with stable signs; No previous neuropsychiatric-related diseases; No significant impairment of cognitive function and able to cooperate in completing the corresponding rehabilitation training; With unilateral upper limb dysfunction; Patients who have not received various neuromodulation rehabilitation treatments; No contraindications to taVNS; Patients voluntarily cooperated with the study and signed an informed consent form. Exclusion Criteria: Patients have other mental health disorders (dementia, Parkinson's disease, depression, schizophrenia, bipolar disorder, etc.) Patients have uncontrolled epilepsy, i.e., having had a seizure within 4 weeks prior to enrollment Patients have cardiac arrhythmias or other abnormalities Patients have a history of respiratory disease or disorder, including dyspnea and asthma; The presence of gastrointestinal disorders such as diarrhea and vomiting that make it difficult for the patient to cooperate Patients have a history of vasovagal syncope Patients are under treatment with other neurostimulation/modulation The presence of severe spasticity, other serious injuries to the upper extremities, or other medical conditions Patients have difficulty in communication and understanding and inability to cooperate in completing the test; Women who are pregnant or breastfeeding.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xue-Zhen XIAO, PhD
Phone
+8613425122570
Email
xuezhenxiao@brainclos.com
First Name & Middle Initial & Last Name or Official Title & Degree
Rongdong Li, BSc
Phone
+86 15626216282
Email
13413627078@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Qiuyou Xie, PhD
Organizational Affiliation
Southern Medical University, China
Official's Role
Principal Investigator
Facility Information:
Facility Name
Zhujiang Hospital of Southern Medical University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510280
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Qiuyou Xie, PhD
Phone
+86 139 0301 9604
Email
764942251@qq.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33894832
Citation
Dawson J, Liu CY, Francisco GE, Cramer SC, Wolf SL, Dixit A, Alexander J, Ali R, Brown BL, Feng W, DeMark L, Hochberg LR, Kautz SA, Majid A, O'Dell MW, Pierce D, Prudente CN, Redgrave J, Turner DL, Engineer ND, Kimberley TJ. Vagus nerve stimulation paired with rehabilitation for upper limb motor function after ischaemic stroke (VNS-REHAB): a randomised, blinded, pivotal, device trial. Lancet. 2021 Apr 24;397(10284):1545-1553. doi: 10.1016/S0140-6736(21)00475-X.
Results Reference
background
PubMed Identifier
35334250
Citation
Liu Y, Zhang L, Zhang X, Ma J, Jia G. Effect of Combined Vagus Nerve Stimulation on Recovery of Upper Extremity Function in Patients with Stroke: A Systematic Review and Meta-Analysis. J Stroke Cerebrovasc Dis. 2022 Jun;31(6):106390. doi: 10.1016/j.jstrokecerebrovasdis.2022.106390. Epub 2022 Mar 22.
Results Reference
background
PubMed Identifier
36683127
Citation
De Smet S, Ottaviani C, Verkuil B, Kappen M, Baeken C, Vanderhasselt MA. Effects of non-invasive vagus nerve stimulation on cognitive and autonomic correlates of perseverative cognition. Psychophysiology. 2023 Jun;60(6):e14250. doi: 10.1111/psyp.14250. Epub 2023 Jan 22.
Results Reference
background
PubMed Identifier
34899170
Citation
Chang JL, Coggins AN, Saul M, Paget-Blanc A, Straka M, Wright J, Datta-Chaudhuri T, Zanos S, Volpe BT. Transcutaneous Auricular Vagus Nerve Stimulation (tAVNS) Delivered During Upper Limb Interactive Robotic Training Demonstrates Novel Antagonist Control for Reaching Movements Following Stroke. Front Neurosci. 2021 Nov 25;15:767302. doi: 10.3389/fnins.2021.767302. eCollection 2021.
Results Reference
background
PubMed Identifier
32289710
Citation
Cook DN, Thompson S, Stomberg-Firestein S, Bikson M, George MS, Jenkins DD, Badran BW. Design and validation of a closed-loop, motor-activated auricular vagus nerve stimulation (MAAVNS) system for neurorehabilitation. Brain Stimul. 2020 May-Jun;13(3):800-803. doi: 10.1016/j.brs.2020.02.028. Epub 2020 Feb 27.
Results Reference
background
PubMed Identifier
25288536
Citation
Monge-Pereira E, Molina-Rueda F, Rivas-Montero FM, Ibanez J, Serrano JI, Alguacil-Diego IM, Miangolarra-Page JC. Electroencephalography as a post-stroke assessment method: An updated review. Neurologia. 2017 Jan-Feb;32(1):40-49. doi: 10.1016/j.nrl.2014.07.002. Epub 2014 Oct 5. English, Spanish.
Results Reference
background
PubMed Identifier
37209010
Citation
Badran BW, Peng X, Baker-Vogel B, Hutchison S, Finetto P, Rishe K, Fortune A, Kitchens E, O'Leary GH, Short A, Finetto C, Woodbury ML, Kautz S. Motor Activated Auricular Vagus Nerve Stimulation as a Potential Neuromodulation Approach for Post-Stroke Motor Rehabilitation: A Pilot Study. Neurorehabil Neural Repair. 2023 Jun;37(6):374-383. doi: 10.1177/15459683231173357. Epub 2023 May 20.
Results Reference
background

Learn more about this trial

taVNS Paired With Motor Training for Upper-extremity Rehabilitation in Stroke Patients

We'll reach out to this number within 24 hrs