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Exploring the Molecular Mechanisms and Prevention Strategies of Post-Stroke Cognitive Impairment (PSCI) Based on Multi-Tissue Integrated Metabolomics

Exploring the Molecular Mechanisms and Prevention Strategies of Post-Stroke Cognitive Impairment (PSCI) Based on Multi-Tissue Integrated Metabolomics

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100295
Enrollment
Unknown
Registered
2025-04-07
Start date
2024-05-14
Completion date
Unknown
Last updated
2025-04-14

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

Conditions

PSCI

Interventions

PSCI Group:Medication treatment + conventional cognitive function training
Non-PSCI group:NA

Sponsors

Shanghai University of Medicine & HealthScienceAffiliated Zhoupu Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to 95 Years

Inclusion criteria

Inclusion criteria: 1. Age range: The inclusion criteria are set for ages 55 to 95 years. 2. Stroke diagnosis: The inclusion criteria include patients with a history of ischemic or hemorrhagic stroke for more than 6 months, confirmed by brain imaging (e.g., cranial CT or MRI). 3. Cognitive impairment diagnosis: The inclusion criteria require a clear clinical diagnostic standard for cognitive impairment, such as DSM-5 (Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition) or NINDS-AIREN (National Institute of Neurological Disorders and Stroke-Association Internationale pour la Recherche et l'Enseignement en Neurosciences criteria for vascular dementia). 4. Cognitive function assessment: Use standardized cognitive assessment tools (e.g., MMSE or MoCA) for evaluation, with inclusion criteria requiring patients’ scores to meet the diagnostic standards for cognitive impairment. 5. Non-targeted metabolomics data collection: Specify the type of biological samples to be collected (e.g., blood, feces) and the time points for collection to facilitate metabolomics analysis. 6. Consent to participate: The inclusion criteria require patients to understand the purpose and procedures of the study and to sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Other neurological diseases: Exclude patients diagnosed with other confirmed neurological disorders such as Alzheimer’s disease, Parkinson’s disease, or frontotemporal dementia to ensure that the primary cause of cognitive impairment in the study subjects is post-stroke cognitive impairment (PSCI). 2. Severe organic brain lesions: Exclude patients with severe organic brain lesions, such as intracranial space-occupying lesions or intracranial hemorrhage, to avoid interference from other lesions on cognitive impairment. 3. Cardiovascular diseases: Exclude patients with other severe cardiovascular diseases, such as myocardial infarction or heart failure, to reduce the impact of cardiovascular factors on cognitive function. 4. Severe psychiatric disorders: Exclude patients with significant mental illnesses, such as severe depression or severe anxiety, to ensure that cognitive impairment is caused by stroke. 5. Severe liver or kidney dysfunction: Exclude patients with significant liver or kidney dysfunction to avoid their influence on metabolomics analysis.

Design outcomes

Primary

MeasureTime frame
minimental status evaluation, MMSE;

Secondary

MeasureTime frame
Activities of Daily Living scale;fNIRS;Montreal cognitive assessment,MoCA;

Countries

China

Contacts

Public ContactZhou Yumin

Shanghai University of Medicine &HealthScienceAffiliated Zhoupu Hospital

z536553089@163.com+86 150 0294 3463

Outcome results

None listed

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