Vascular Dementia Clinical Trials

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Development of a Genomics-based Multimodal Prediction Model for Post-stroke Vascular Dementia: An Ambidirectional Patient-Control Cohort Study

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

To collect large-scale multimodal data, including genomic information, neuroimaging, neurophysiological measures, cognitive assessments, and clinical characteristics from stroke survivors and healthy controls. This study aims to develop and validate an integrated prediction model for identifying individuals at high risk of post-stroke vascular dementia and to establish a foundation for precision medicine approaches in stroke-related cognitive impairment.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Healthy Volunteers: t
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• Healthy Control Group:

‣ Adults aged 19 years or older.

⁃ Able to be age- and sex-matched to the stroke cohort.

⁃ No history of stroke, transient ischemic attack (TIA), or other central nervous system disorders.

⁃ Cognitive function within the normal range for age and education level based on screening assessments (K-MMSE and K-MoCA).

⁃ Able to understand the study procedures and provide written informed consent.

• Stroke Patient Group:

‣ Adults aged 19 years or older.

⁃ First-ever ischemic or hemorrhagic stroke confirmed by CT or MRI.

⁃ Enrolled in one of the following strata according to time since stroke onset:

∙ Stratum A: 7 days to 3 months after stroke onset. Stratum B: \>3 months to 12 months after stroke onset. Stratum C: \>12 months to 36 months after stroke onset.

∙ \- Able to understand the study procedures and provide written informed consent, or consent provided by a legally authorized representative when applicable.

Locations
Other Locations
Republic of Korea
Bundang CHA Medical Center
RECRUITING
Gyeonggi-do
Contact Information
Primary
Seyoung Shin, MD
seyoung0706@chamc.co.kr
+82437505000
Time Frame
Start Date: 2026-07-24
Estimated Completion Date: 2030-12-31
Participants
Target number of participants: 300
Treatments
Stroke patients
Adults aged 19 years or older with first-ever ischemic or hemorrhagic stroke. Participants may be enrolled during the subacute or chronic stage after stroke and will undergo genomic, neuroimaging, neurophysiological, cognitive, and functional assessments with longitudinal follow-up for up to 36 months.
Healthy controls
Cognitively normal adults aged 19 years or older without a history of stroke, transient ischemic attack, or other major central nervous system disorders. Participants will undergo genomic, neuroimaging, neurophysiological, cognitive, and functional assessments and follow-up evaluations.
Sponsors
Leads: Seyoung Shin

This content was sourced from clinicaltrials.gov