Key Technical Research on the Treatment of Post-stroke Cognitive Impairment With Brain Electric Field Therapy Based on Acupoint Regulation

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age35-80
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

About this trial

This clinical study investigates whether electroacupuncture can improve thinking and memory in people with cognitive problems after a stroke (Post-Stroke Cognitive Impairment, or PSCI).

Participants will be randomly assigned to one of two groups: one group will receive real electroacupuncture, while the other will receive a sham treatment . Both groups will also receive standard medical care.The main goal is to see if the real electroacupuncture leads to greater improvement in cognitive function tests over 6 months compared to the sham treatment. The study will also use brain scans (MRI) and other assessments to understand how the treatment might work.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Meets diagnostic criteria for Vascular Cognitive Impairment (VCI) per the 2024 Chinese VCI guidelines.

Meets TCM diagnostic criteria per the 2024 Vascular Mild Cognitive Impairment guidelines.

Cognitive scores: MMSE 12-24 and MoCA <24; NIHSS ≤8; AD-8 <2.

Age 35-80 years.

Disqualifiers

Severe chronic systemic diseases (e.g., cardiac, hepatic, renal, hematologic) or unstable cardiovascular/cerebrovascular disease.

Local skin conditions (e.g., herpes, ulceration, keloid) contraindicating acupuncture.

Contraindications for repeated MRI (e.g., claustrophobia, post-aneurysm embolization).

Pre-existing cognitive impairment or other major uncontrolled neurological/psychiatric disorders.

Trial design

Design model

Parallel

Treatments tested in this trial

  • True Electroacupuncture

    Procedure/Surgery

    The true electroacupuncture group will receive electroacupuncture treatment for 7 days, once a day, each session lasting approximately 30 minutes. Acupoints include main points (e.g., bilateral forehead lines, Tianzhu BL10, Fengchi GB20) and syndrome-based points. After needle insertion and manual stimulation for deqi, true EA (100 Hz dense wave, tolerable intensity) is applied the SDZ-IIB device, connecting MS2 and BL10 on each side.

  • Sham Electroacupuncture

    Procedure/Surgery

    The sham electroacupuncture group will receive electroacupuncture treatment for 7 days, once a day, each session lasting approximately 30 minutes.The same acupoints and needle insertion/manual stimulation are used. However, a modified SDZ-IIB device with severed leads (incapable of current output) is connected, simulating the appearance of true electroacupuncture without electrical stimulation. The treatment frequency and duration are identical to the electroacupuncture group.

Treatment groups

110 Participants
are divided into 2 treatment groups
Group A: True ElectroacupunctureExperimental treatment 1 intervention
Group B: Sham ElectroacupunctureSham comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change in Mini-Mental State Examination (MMSE) Score

The Mini-Mental State Examination (MMSE) is a standardized 30-point questionnaire used to screen for cognitive impairment. Total scores range from 0 to 30, with higher scores indicating better cognitive function.

Time frame
baseline, 3 months and 6 months post-treatment.
2

Change in MoCA (Montreal Cognitive Assessment) Scale Score

The Montreal Cognitive Assessment (MoCA) is a 30-point screening tool designed to detect mild cognitive impairment. Total scores range from 0 to 30, with higher scores indicating better cognitive function.

Time frame
baseline, 3 months and 6 months post-treatment.
3

Change in Clinical Dementia Rating (CDR) scale Score

The Clinical Dementia Rating (CDR) is a clinician-rated scale that assesses the severity of dementia across six domains. The global CDR score ranges from 0 (no impairment) to 3 (severe dementia), with higher scores indicating greater severity of dementia.

Time frame
baseline, 3 months and 6 months post-treatment.
4

Change in NTB (Neuropsychological Test Battery) Score

The Neuropsychological Test Battery (NTB) is a composite measure designed to assess cognitive function across multiple domains. It evaluates key areas including memory (e.g., verbal/visual recall), attention, executive function, and processing speed. A composite Z-score is derived by averaging the standardized scores of the individual cognitive tests. The composite score is interpreted such that higher scores indicate better overall cognitive performance.

Time frame
baseline, 3 months and 6 months post-treatment.

Secondary outcomes

1

Multimodal functional Near-Infrared Spectroscopy - Electroencephalogram (fNIRS-EEG) Assessment

Functional Near-Infrared Spectroscopy (fNIRS) and Electroencephalogram (EEG) are used to non-invasively record cerebral hemodynamic changes (blood oxygen levels and blood flow) and electrophysiological brain activity, respectively, to explore neural correlates of treatment response.

Time frame
baseline, 3 months, and 6 month
2

Quality of Life as assessed by the Stroke-Specific Quality of Life Scale (SS-QOL)

The Stroke-Specific Quality of Life Scale (SS-QOL) is a patient-reported outcome measure designed to evaluate health-related quality of life specifically for stroke survivors. It assesses multiple domains relevant to life after stroke. Scores are calculated for each domain and a total score can be derived, with higher scores indicating better perceived quality of life.

Time frame
baseline, 3 months, and 6 months.
3

Depressive Symptoms as assessed by the Hamilton Depression Rating Scale (HRSD-24)

The Hamilton Depression Rating Scale (HRSD-24) is a clinician-administered scale used to rate the severity of depressive symptoms. Higher total scores indicate greater severity of depression.

Time frame
baseline, 3 months, and 6 months
4

Traditional Chinese Medicine (TCM) Syndrome Score

A diagnostic scale based on the TCM Diagnostic and Treatment Guidelines for Vascular Mild Cognitive Impairment (2024). It evaluates TCM symptoms, tongue, and pulse features to diagnose syndrome patterns (e.g., Kidney Deficiency with Blood Stasis). A total score ≥12 confirms the diagnosis of a specific syndrome pattern.

Time frame
baseline, 3 months, and 6 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Second Affiliated Hospital, School of Medicine, Zhejiang University

Lead sponsor

The Third Affiliated hospital of Zhejiang Chinese Medical University

Collaborator

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