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Electroacupuncture Treatment for Post-stroke Cognitive Impairment

Study on the Key Technology of Acupoint Modulation-based Brain Electric Field Therapy for the Treatment of Post-stroke Cognitive Impairment

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07208019
Enrollment
340
Registered
2025-10-06
Start date
2025-10-05
Completion date
2027-03-30
Last updated
2025-12-17

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

Conditions

Post-Stroke Cognitive Impairment (PSCI)

Keywords

Stroke, PSCI, Post-stroke cognitive impairment

Brief summary

Stroke is a global public health issue, and it has become a leading cause of death and disability in China. With the rapid aging of the Chinese population, its incidence rate is continuously rising. According to the China Stroke Prevention and Treatment Report (2023), on average, one person experiences a new or recurrent stroke every 10 seconds in China, and one person dies from stroke every 28 seconds. Currently, there are 4 million new stroke cases in China each year, with 12.42 million individuals aged 40 and above currently suffering from stroke, and the affected population is showing a trend of younger onset. Among survivors, approximately 75% suffer from residual disabilities, and 40% have severe disabilities. Consequently, patient families will experience significant economic losses and physical and psychological pain. Post-Stroke Cognitive Impairment (PSCI) is a common complication of stroke, where patients develop cognitive impairment within six months after the stroke event that meets the diagnostic criteria for cognitive impairment. PSCI is defined as a clinical phenomenon secondary to stroke events, with cognitive decline as its core characteristic. Such impairments encompass cognitive dysfunction caused by various stroke types and are one of the main determinants of functional dependency in post-stroke survivors. The prevalence of PSCI within six months is approximately 30% to 50%, with 10% progressing to dementia. Additionally, PSCI patients face a high risk of death, with up to 61% dying within five years. Countries worldwide have launched targeted guidelines, calling for increased attention and investment in this major complication. However, current treatments for PSCI are still limited to secondary prevention measures for stroke and drugs for treating Alzheimer's disease-like conditions, all lacking high-level clinical evidence. Therefore, effective treatments are urgently needed to improve patient outcomes. PSCI is a dynamically evolving process, with individual differences in its occurrence time, influencing factors, clinical manifestations, and recovery prognosis. The unique diagnostic system of traditional Chinese medicine may assist in analyzing the disease progression of PSCI. The study of the patterns of syndrome evolution can help explain and provide reference for treatment. Currently, there are no specific drugs for treating PSCI, and relevant drug treatments lack high-level evidence. In recent years, with the development of imaging, artificial intelligence, and electromagnetic physics, non-pharmacological therapies have gradually become one of the research hotspots in the field of PSCI. It is worth noting that non-invasive brain stimulation, represented by transcranial electrical stimulation, is a therapy that directly acts on the brain lesions of PSCI and is often used in combination with acupoint stimulation to achieve better therapeutic effects. Meanwhile, acupuncture and moxibustion therapy has demonstrated good efficacy and safety in the prevention and treatment of PSCI. Multiple clinical studies suggest that electroacupuncture therapy can improve cognitive impairment in patients with PSCI and enhance their quality of life. Furthermore, electroacupuncture therapy can also provide targeted treatment for patients through syndrome differentiation and treatment, compensating for the limitations of Western medicine drug therapy. This study aims to investigate the evolution patterns of syndromes in post-stroke cognitive impairment (PSCI). Simultaneously, through the standardization of multidimensional and multimodal data related to PSCI patients, we will conduct a multicenter, large-sample clinical randomized controlled trial of electroacupuncture intervention for PSCI using a multimodal artificial intelligence big data model. The goal is to establish a characteristic technology for the diagnosis and treatment of PSCI in traditional Chinese medicine (TCM) that is suitable for promotion, and to establish clinical diagnosis and treatment pathways and standard specifications for diseases where TCM has advantages. This will facilitate the establishment of an efficacy evaluation system for PSCI based on TCM syndrome diagnosis and evolution patterns, realize a precise diagnosis and treatment model combining traditional Chinese and Western medicine for PSCI, and improve patients' overall efficacy and quality of life.

Interventions

OTHERAcupuncture

Electroacupuncture group: After local routine disinfection.Select the main acupoints of bilateral frontoparietal line (MS2), Tianzhu (BL10), Fengchi (GB20), blood supply, parietal midline (MS5), and parietal midline (MS8). Connect the wires of the electroacupuncture instrument to the same side of the bilateral frontoparietal line(MS2) and Tianzhu acupoint (BL10), and perform head electroacupuncture treatment on both sides with a pair on each side.There are two groups of electroacupuncture, with a continuous frequency of 100Hz, and each electroacupuncture stimulation lasts for 30 minutes. After enrollment, treatment will be conducted 5 times a week for 8 weeks.

Sponsors

Second Affiliated Hospital, School of Medicine, Zhejiang University
CollaboratorOTHER
The Third Affiliated hospital of Zhejiang Chinese Medical University
CollaboratorOTHER
The First Affiliated Hospital of Zhejiang Chinese Medical University
CollaboratorOTHER
Hangzhou Hospital of Traditional Chinese Medicine
CollaboratorOTHER
Zhejiang Provincial People's Hospital
CollaboratorOTHER
Ruijie Ma
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

In the whole research process the principle of three separations was implemented: the three parties of operators efficacy evaluators and statistical analysts were separated and the three parties could not exchange research data implementation and other related contents during the whole process of the study. That is to say the third-party professional statisticians who did not know the grouping situation carried out the efficacy evaluation and statistical analysis of the result data in order to try to avoid the bias of the data results caused by single blinding.

Eligibility

Sex/Gender
ALL
Age
35 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* According to the Western diagnostic criteria for vascular cognitive impairment outlined in the Chinese Guidelines for the Diagnosis and Treatment of Vascular Cognitive Impairment (2024 Edition) developed by the Vascular Cognitive Impairment Branch of the Chinese Stroke Society. * Meets the traditional Chinese medicine diagnostic criteria for vascular cognitive impairment in the Guidelines for Traditional Chinese Medicine Diagnosis and Treatment of Vascular Mild Cognitive Impairment (2024); * The Mini Mental State Examination (MMSE) score ranges from 12-24, while the Montreal Cognitive Assessment (MoCA) score is below 24; Having cognitive impairment but not reaching the level of severe dementia; The National Institutes of Health Stroke Scale (NIHSS) score is ≤ 8 points; The Early Dementia Screening Scale (Ascertain Dementia 8, AD-8) score is less than 2 points; * Age between 35-80 years old; * Have basic communication skills, with Mandarin as the main language (communication language is sufficient), and have at least one stable caregiver; * Sign the informed consent form.

Exclusion criteria

* Merge serious primary chronic diseases such as heart, liver, kidney, endocrine system, and hematopoietic system, as well as severe cardiovascular and cerebrovascular diseases; * Skin diseases or scar constitution such as herpes and ulceration are easy to appear on the body surface, which is not suitable for acupuncture and moxibustion treatment; * Not suitable for repetitive MRI examinations, such as claustrophobia, arterial aneurysm embolization, etc; * Patients with cognitive impairment or other severe neurological or mental disorders prior to the onset of this illness, and unstable control; * Patients identified by other clinical trial personnel as unsuitable for this study; * Participated in clinical research on related diseases in the past 3 months;

Design outcomes

Primary

MeasureTime frame
Neuropsychological Test Battery(NTB)Week 0 before treatment, Week 12 after treatment, Week 24 after treatment
Montreal Cognitive AssessmentWeek 0 before treatment, Week 12 after treatment, Week 24 after treatment
Mini-Mental State ExaminationWeek 0 before treatment, Week 12 after treatment, Week 24 after treatment

Secondary

MeasureTime frameDescription
Electroencephalogram(EEG)Pre-treatment, 8th week post-treatmentEvaluate the quantitative electroencephalogram parameters alpha wave, beta wave, delta wave, and theta wave absolute power, as well as the (delta+theta)/(alpha+beta) ratio (DTABR) and delta/alpha power ratio (DAR), and analyze the correlation between various parameters and cognitive function.
Near-infrared spectroscopyPre-treatment, 8th week post-treatment
Magnetic Resonance ImagingPre-treatment, 8th week post-treatment
Pittsburgh sleep quality index(PSQI)Week 0 before treatment, Week 12 after treatment, Week 24 after treatmentIt consists of seven dimensions: subjective sleep quality, falling asleep time, sleep duration, sleep disturbances, use of hypnotic drugs, daytime functional disorders, and sleep efficiency. Each dimension scores 0-3 points, with a minimum score of 0 and a maximum score of 21 points. The higher the score, the more severe the sleep problem. The total score of the seven dimensions is the PSQI score.
Short Form 12 Health Survey(SF-12)Week 8 after treatmentThis scale covers eight aspects: physical function, physical role, pain, general health, mental health, social function, emotional role, and psychological health. The overall score range is 0-100 points, with higher scores indicating better health conditions.
Modified Rankin Scale(mRS)Week 0 before treatment, Week 12 after treatment, Week 24 after treatmentThe scoring criteria are 0-5 points, with 0 being completely asymptomatic and 5 being severely disabled.
Modified Barthel IndexWeek 0 before treatment, Week 12 after treatment, Week 24 after treatment
Hamilton Depression Scale(HAMD)Week 0 before treatment, Week 12 after treatment, Week 24 after treatment\<7 indicates no, 7-17 indicates possible, 17-24 indicates certain,\>24 indicates severe depression. The lowest score is 0, and the highest score is 46. The higher the score, the more severe the patient's depression.

Countries

China

Contacts

Primary ContactBowen Chen
cbwwjj@163.com+86 13967988987
Backup ContactLuyao Fu
1710591584@qq.com+86 18457100195

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026