Skip to content

A Clinical Trail of Integrative Medicine Approaches for Post-Stroke Cognitive Impairment

A Clinical Trail of Integrative Medicine Approaches for Post-Stroke Cognitive Impairment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04596072
Enrollment
122
Registered
2020-10-22
Start date
2019-04-25
Completion date
2024-12-31
Last updated
2025-04-29

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

Conditions

Post-stroke Cognitive Impairment

Keywords

post-stroke cognitive impairment, rehabilitation, traditional Chinese medicine

Brief summary

The traditional Chinese medicine rehabilitation for the post-stroke cognitive impairment will be intervened, which can promote the recovery of post-stroke cognitive function patients, reduce the disability rate and improve the quality of life.

Detailed description

This study will collect inpatients from April 2019 to December 2024 who from the third affiliated hospital of Zhejiang university of traditional Chinese medicine, Jiaxing hospital of traditional Chinese medicine, Hangzhou hospital of traditional Chinese medicine.this study sets strict time window (stroke recovery, 30-180 days), use multi-center, large sample, randomized controlled study method and the objective recognition rehabilitation evaluation criteria and efficacy evaluation system to evaluate the clinical effect and analysis of health economics.

Interventions

COMBINATION_PRODUCTChinese traditional rehabilitation

Chinese traditional rehabilitation including acupuncture and herbs

Sponsors

The Third Affiliated hospital of Zhejiang Chinese Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Stroke as per the TCM definition, presenting symptoms include unilateral paresis or paralysis, sensory deficits, speech impairment, and hemianopsia. PSCI diagnosis involves clinically significant deficits in at least one cognitive domain and severe disruption of instrumental activity of daily livings. 2. age above 18 years; 3. disease duration of 30-180 days; 4. written informed consent by the patient's legal guardian; 5. MoCA (Montreal Cognitive Assessment) score of 17-26. If patient was educated for ≤ 12 years, one score will be deducted; 6. HAMD(Hamilton Depression Scale) score \< 20; 7. indications for acupuncture and moxibustion techniques.

Exclusion criteria

1. Cognitive impairment caused by subarachnoid hemorrhage, transient ischemic attack, or other intracranial lesions., such as tumors, aneurysms, vascular malformations, cysticercosis, schistosomiasis, encephalitis, meningitis, hydrocephalus, or head trauma; 2. non-atherosclerotic thrombotic cerebral infarction (such as cardiac embolism, procoagulant state, endovascular shedding, or arteritis); 3. pregnant or lactating women; 4. severe chronic diseases of the heart, liver, kidneys, other viscera, or endocrine system or hematopoietic system; 5. severe dementia, serious language understanding disorders, or mental illness; 6. bleeding tendency; 7. lack of inclusion criteria or not suitable for clinical observation.

Design outcomes

Primary

MeasureTime frameDescription
Change of Cognitive function0 week, 4 weeks, 8 weeks, 12 weeks, 16weeksMontreal Cognitive Assessment(MOCA) will be used, this method focus on the sensitivity and specificity of the scale for the recognition of cognitive impairment are high, and it is evaluated from visual spatial/executive function, language function, image ability orientation and so on. MoCA has a maximum score of 30 points. The normal scoring standard is a total score ≥ 26 points (for those with an education level ≤ 12 years, this standard is reduced by 1 point). Higher scores mean a better outcome.

Secondary

MeasureTime frameDescription
change in the scores of mini-Mental State Examination (MMSE)0 week, 8 weeks, 12 weeks, 16 weeksThe scale is used for rapid evaluation of orientation, memory, attention, calculation, language, and visuospatial structure. MMSE has a maximum score of 30 points. The normal cut-off values are: illiterate group ≥17 points, primary school group ≥20 points, middle school or higher group ≥24 points. Higher scores mean a better outcome.
Changes in Daily Living ability0 week, 8 weeks, 12 weeks, 16 weeksADL(Activity of Daily Living) will be used, which also known as the Barthel Index, consists of 10 items, including toileting, grooming, using the toilet, eating, dressing, transferring, activities, going up and down stairs, and bathing). The total score ranges from 0 to 100. Higher scores mean a better outcome.
Changes in depressive status0 week, 8 weeks, 12 weeks and 16 weeksuse Hamilton Depression Scale to evaluate depression, the score were 24 for severe, 17 for moderate and 7 for mild. Higher scores mean a worse outcome.
Changes in the patterns of activation of brain regions related to cognitive impairment0 weeks, 8 weeksALLF, fALFF, PerAF, ReHo and DC were used to analyze the resting state functional magnetic resonance imaging. The pattern changes of relevant brain regions related to cognitive impairment after stroke were revealed.

Countries

China

Outcome results

None listed

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