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Effects of Transcutaneous Auricular Vagus Nerve Stimulation on Upper Limb Motor Function in Patients with Cerebral Hemorrhage

Effects of Transcutaneous Auricular Vagus Nerve Stimulation on Upper Limb Motor Function in Patients with Cerebral Hemorrhage

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121762
Enrollment
Unknown
Registered
2026-04-02
Start date
2026-03-08
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Upper limb motor dysfunction after intracerebral hemorrhage

Interventions

taVNS Group:A portable transcutaneous nerve stimulation device was adopted, with electrodes placed in the left auricular concha area. The stimulation parameters were set as follows: frequency at 25 Hz
Sham Stimulation Group:An identical device with the same appearance and operation mode as that used in the intervention group was applied, with electrodes placed on the earlobes and the current intens

Sponsors

Deqing County People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 75 years old; 2. First-ever intracerebral hemorrhage confirmed by cranial computed tomography (CT) or magnetic resonance imaging (MRI); 3. Unilateral hemiplegia complicated with upper limb motor dysfunction, with a Fugl-Meyer Assessment of Upper Extremity (FMA-UE) score ranging from 20 to 50; 4. Signed informed consent obtained from the patient or their legal representative.

Exclusion criteria

Exclusion criteria: 1. Comorbid with other neurological disorders that may impair motor function; 2. Severe cognitive impairment or aphasia, rendering the subject unable to cooperate with assessments and treatment; 3. Contraindications to transcutaneous auricular vagus nerve stimulation (taVNS), including local ear diseases or injuries, severe cardiovascular diseases, or implanted medical devices; 4. Pregnant or lactating women; 5. High risk of bleeding or abnormal coagulation function.

Design outcomes

Primary

MeasureTime frame
Changes in Fugl-Meyer Assessment of Upper Extremity (FMA-UE) score;

Secondary

MeasureTime frame
Brunnstrom Recovery Stages (BRS);Modified Barthel Index (MBI);Incidence of adverse events;

Countries

China

Contacts

Public ContactWang Yunhui

Neurosurgery Department, Deqing County People's Hospital

13567260703@163.com+86 135 6726 0703

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026