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Study on the efficacy and mechanism of acupuncture in early intervention of PSA based on structural brain network-brain age

Study on the efficacy and mechanism of acupuncture in early intervention of PSA based on structural brain network-brain age

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000113
Enrollment
Unknown
Registered
2025-01-15
Start date
2025-02-05
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

post-stroke aphasia

Interventions

Experimental group:"Yisui Xingshen" acupuncture+Basic medical therapy+Language rehabilitation training
Control group:Non-channel non-point fake acupuncture+Basic medical therapy+Language rehabilitation training

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 80 Years

Inclusion criteria

Inclusion criteria: A The diagnosis meets the ischemic stroke disease criteria in the Chinese guidelines for diagnosis and treatment of acute ischemic stroke 2018 and the onset time of the patient is within 14-30 days (including 14 and 30 days); B Motor Aphasia was diagnosed by the Western Aphasia Battery (WAB); C The severity of the patient's Aphasia was assessed by the Boston Diagnostic Aphasia Examination (BDAE) at 2-4 grades which could be assessed with the linguistic scale; D Right-handed (left-brain advantage) native speaker of Chinese patients regardless of gender between 35 and 80 years old (including 35 and 80 years old) with primary school education or above; E The condition was stable with unconsciousness disorder and no other non-vascular cognitive dysfunction; F There is no metal in the body and no contraindications for MRI and the patient can cooperate to complete the 20-minute MRI.

Exclusion criteria

Exclusion criteria: A Patients with severe non-verbal cognitive auditory visual or phonological dysfunction resulting in inability to cooperate with the scale evaluation; B Language dysfunction due to congenital or childhood disease; C Being pregnant or lactating; D With bleeding tendencies; E Patients with serious abnormalities of heart liver kidney and other important organs are deemed unfit to participate in this study after evaluation; F Patients with implanted pacemakers or those with severe arrhythmias or local skin infections.

Design outcomes

Primary

MeasureTime frame
Changes in Aphasia Quotient after 4 weeks of intervention ;

Secondary

MeasureTime frame
Changes in MMSE score after 4 weeks of intervention and 90 days after enrollment;Changes in Aphasia Quotient after 90 days of enrollment;Changes in daily living ability score after 4 weeks of intervention and 90 days after enrollment;Changes in NIHSS score after 4 weeks of intervention and 90 days after enrollment;Changes of structural brain network and brain age difference after 4 weeks of intervention;Changes in MoCA score after 4 weeks of intervention and 90 days after enrollment;

Countries

China

Contacts

Public ContactJiaqin Huang

Beijing Hospital

15652609751@163.com15652609751

Outcome results

None listed

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