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Study on the Efficacy and Mechanism of Action of Electrical Stimulation for Dysphagic Patients in the Post-Stroke Recovery Period

Study on the therapeutic effects and mechanism of electrical stimulation in dysphagic patients during the post-stroke recovery period.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002642
Enrollment
Unknown
Registered
2025-12-30
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Swallowing disorders in the recovery period of stroke

Interventions

Routine Rehabilitation Group:Routine rehabilitation therapy
Conventional rehabilitation + Electroacupuncture group:Routine rehabilitation + electroacupuncture therapy

Sponsors

Zhejiang University of Traditional Chinese Medicine Affiliated Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Patients diagnosed with stroke via CT or MRI; (2) Aged between 35 and 80 years old; (3) Disease onset within 2 weeks to 6 months, with stable vital signs in the past week; (4) Confirmed to have dysphagia via Flexible Endoscopic Evaluation of Swallowing (FEES) or Video Fluoroscopic Swallowing Study (VFSS); (5) Able to cooperate with the assessment and willing to sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Pregnant or breastfeeding women; (2) Individuals with complete motor aphasia or sensory aphasia, or local lesions in the throat such as thyroid diseases, local infections, or ulcers; (3) Individuals with excessively high blood pressure (>180/120 mmHg) or blood glucose (>11.1 mmol/L) that remains uncontrolled; (4) Individuals with bleeding tendencies or other conditions that affect the safety of acupuncture; (5) Individuals with severe diseases of the kidneys, liver, heart, blood, or endocrine system; (6) Individuals with intellectual disabilities or psychiatric symptoms that prevent cooperation with treatment; (7) Individuals with a tracheostomy.

Design outcomes

Primary

MeasureTime frame
Flexible Laryngoscope Swallowing Function Assessment;Swallowing radiographic examination;Leakage Aspiration Grading;

Secondary

MeasureTime frame
Standardized Swallowing Function Assessment;Functional Near-Infrared Spectroscopy Imaging;

Countries

China

Contacts

Public ContactKang Liang

Zhejiang University of Traditional Chinese Medicine Affiliated Third Hospital

392436797@qq.com18868850120

Outcome results

None listed

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