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Effects of electroacupuncture on post-stroke dysphagia: a randomized controlled trial

Effects of electroacupuncture on post-stroke dysphagia: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000216
Enrollment
Unknown
Registered
2024-08-12
Start date
2024-08-15
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Post-stroke dysphagia

Interventions

Electroacupuncture group:Electroacupuncture+Swallowing training
Sham Electroacupuncture group:Sham Electroacupuncture+Swallowing training

Sponsors

The Second Affiliated Hospital of Heilongjiang University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with stroke according to the 2019 guidelines of the National Institute for Health and Care Excellence (NICE) and confirmed by cranial CT or MRI; 2. Aged between 20 and 80 years, regardless of gender; 3. Stroke onset between 7 days and 3 months with newly developed dysphagia; 4. PAS score of 3 or higher in VFS/FEES screening protocol; 5. NIHSS-1a score of 0 or 1; 6. Cooperate with various examinations and rehabilitation training; 7. Voluntary participation in the trial and signed written informed content.

Exclusion criteria

Exclusion criteria: 1. History of dysphagia; 2. Severe cognitive or psychiatric disorders; 3. Pregnant or breastfeeding women; 4. Dysphagia caused by other diseases, such as nasopharyngeal cancer, esophageal cancer, or brain injury; 5. Diagnosed with progressive neurological diseases (e.g., Parkinson's disease, multiple sclerosis); 6. Chronic diseases affecting heart or respiratory conditions (e.g., severe emphysema or heart failure, making neck needling unsafe); 7. Receiving continuous oxygen therapy or equipped with oxygen supply equipment; 8. Participants who have participated in similar clinical studies within the past 3 months.

Design outcomes

Primary

MeasureTime frame
Dysphagia Severity Rating Scale, DSRS;

Secondary

MeasureTime frame
Penetration-Aspiration Score, PAS;Nutritional Risk Screening 2002, NRS-2002;Swallowing Quality of Life, SWAL-QOL;Incidence of Aspiration Pneumonia;Clinical Global Impression Scale, CGI;

Countries

China

Contacts

Public ContactZhu Luwen

The Second Affiliated Hospital of Heilongjiang University of Chinese Medicine

zhuluwen1983@126.com18646026439

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 7, 2026