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A clinical randomised controlled study of auricular vagus nerve electrical stimulation to improve upper limb motor-cognitive function and its central mechanisms in stroke patients

A clinical randomised controlled study of auricular vagus nerve electrical stimulation to improve upper limb motor-cognitive function and its central mechanisms in stroke patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105513
Enrollment
Unknown
Registered
2025-07-04
Start date
2025-07-04
Completion date
Unknown
Last updated
2025-07-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diagnosis of ischaemic or haemorrhagic stroke accompanied by motor dysfunction of the upper limbs according to the diagnostic criteria for cerebrovascular disease

Interventions

Control group (sham stimulation group):sham stimulation
Experimental group (auricular vagus nerve electrical stimulation group):auricular vagus nerve electrical stimulation

Sponsors

The Seventh Affiliated Hospital Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosis of ischaemic or haemorrhagic stroke according to the diagnostic criteria for cerebrovascular disease, after 48 hours of stabilisation, duration of disease = 40 years, <= 79 years; 3.Left or right upper limb dysfunction; 4.right-handed; 5.Ability to remain seated for more than 30 minutes; 6.Ability to communicate, understand and co-operate with instructions and tasks in the research process;

Exclusion criteria

Exclusion criteria: 1.Ongoing use of drugs or interventions that may interfere with the action of the auricular vagus nerve on the neurotransmitter system; 2.Severe or more severe depression, and mental instability; 3.speech impediment; 4.Severe spasticity of the upper limbs (Modified Ashworth Scale score >2); 5.Have progressive hypertension, tumours, recent head injury;

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment for Upper Extremity;Montreal Cognitive Assessment;Action Research Arm Test Assessment;

Secondary

MeasureTime frame
Electroencephalography;functional Near-Infrared Spectroscopy;

Countries

China

Contacts

Public ContactMao Yurong

The Seventh Affiliated Hospital Sun Yat-sen University

maoyr@mail.sysu.edu.cn+86 755 81206511

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026