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Multimodal 30-Day Functional Outcome Prediction Model for Subacute Ischemic Stroke Based on VR Motor-Cognitive Data, Clinical Indicators, and DTI

Multimodal 30-Day Functional Outcome Prediction Model for Subacute Ischemic Stroke Based on VR Motor-Cognitive Data, Clinical Indicators, and DTI

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500111551
Enrollment
Unknown
Registered
2025-11-03
Start date
2025-11-03
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Lschemic stroke

Interventions

Gold Standard:Confirmed by cranial MRI/MRA as infarction in the middle cerebral artery territory
Index test:VR Exercise - Cognitive Function Data?Head MRI Diffusion Tensor Imaging

Sponsors

Zhejiang Provincial Tongde Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with subacute ischemic stroke (meeting the diagnostic criteria of the 2025 version of the "Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke", confirmed by cranial MRI/MRA to have infarction in the middle cerebral artery blood supply area, and the lesion involves the brain regions related to upper limb movement); 2. 7 to 30 days after the onset of the disease, it is within the intervention window period of the subacute stage. 3. Baseline NIHSS score: 3-20 points, FMA-UE score: 32-57 points (with assessable unilateral upper limb motor dysfunction and capable of cooperating with VR motion-cognitive tasks); 4. Clear consciousness (GCS score >=15 points), able to understand and cooperate to complete a 20-minute VR task (MMSE score >=20 points, excluding the interference of cognitive impairment on task execution); 5. No serious musculoskeletal diseases (such as periarthritis of the shoulder, fractures) or history of VR dizziness (no discomfort such as nausea or blurred vision was found in the pre-test); 6. At the 30-day follow-up, the reexamination of FMA-UE (recovery of motor function) and mRS Score (overall functional prognosis) can be completed. 7. Patients and their families who agree to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Hemorrhagic stroke, transient ischemic attack (TIA), or other neurological disorders (such as multiple sclerosis); 2. Unable to cooperate with DTI examination; 3. The quality of DTI data does not meet the standards (such as motion artifacts leading to the failure of corticospinal tract reconstruction); 4. Severe dizziness (such as nausea and vomiting) occurs during VR tasks, making it impossible to complete data collection. 5. Severe heart, liver or kidney diseases or malignant tumors (affecting data stability and follow-up).

Design outcomes

Primary

MeasureTime frame
Head MRI DTI Data;VR Trajectory Quantification Metrics;

Countries

China

Contacts

Public ContactWang Yaqun

Zhejiang Provincial Tongde Hospital

1586997042@qq.com+86 571 8997 5991

Outcome results

None listed

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