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Efficacy of Combined Intradermal Acupuncture and Acupressure in Treating Post-Stroke Dysphagia: A Randomized Controlled Trial

Efficacy of Combined Intradermal Acupuncture and Acupressure in Treating Post-Stroke Dysphagia: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001689
Enrollment
Unknown
Registered
2025-09-09
Start date
2025-08-20
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Post-stroke dysphagia

Interventions

Acupressure Group:Acupressure intervention
Intradermal Needle Group:Intradermal acupuncture intervention
Combined Group:Acupressure combined with intradermal acupuncture intervention

Sponsors

Tongxiang First people's hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosis of stroke and post-stroke dysphagia as defined above; 2.Age between 40 and 80 years; 3.First-ever, unilateral stroke confirmed by history and neuroimaging, with a disease duration between 3 months and 1 year (subacute to chronic phase); 4.KWST score of Grade II or higher, indicating objective swallowing impairment, as assessed by a trained and experienced rehabilitation therapist; 5. No swallowing problems before stroke; 6.Ability to understand study procedures and provide informed consent.

Exclusion criteria

Exclusion criteria: 1. Having had multiple strokes; 2. Presence of acute pharyngeal infection, ulceration, or other local structural abnormalities in the pharynx or esophagus; 3.Significant cognitive impairment, severe aphasia, or psychiatric disorders that would interfere with participation or assessment; 4.History of any formal swallowing rehabilitation therapy (including other forms of acupuncture or physical therapy specifically targeting dysphagia) prior to the current stroke or during the current post-stroke period before enrollment; 5.Dysphagia caused by conditions other than stroke (e.g., neurodegenerative diseases, head and neck tumors, surgery, myasthenia gravis); 6. Having major medical issues that may affect participation in the program; 7. Having had a previous surgical operation or radiotherapy to the head or neck are.

Design outcomes

Primary

MeasureTime frame
Standardized Swallowing Assessment;Experiment of drinking water in depression score;Swallowing Quality of Life;

Secondary

MeasureTime frame
The range of motion of the suprahyoid muscle;The movement time of the suprahyoid muscle;The movement speed of the suprahyoid muscle;

Countries

China

Contacts

Public ContactSu Tingting

Tongxiang First people's hospital

380024681@qq.com18267859581

Outcome results

None listed

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