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Application evaluation of virtual reality training combined with near-infrared brain functional imaging in functional recovery of stroke patients

Application evaluation of virtual reality training combined with near-infrared brain functional imaging in functional recovery of stroke patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088351
Enrollment
Unknown
Registered
2024-08-16
Start date
2024-08-25
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

stroke

Interventions

Test group:Virtual reality training and traditional rehabilitation training

Sponsors

The affiliated hospital of jining medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 69 Years

Inclusion criteria

Inclusion criteria: (1) A newly diagnosed cerebral infarction in the brainstem, basal ganglia, and corona radiation-induced region that meets the diagnostic criteria for ischemic stroke in the 2018 Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke, diagnosed by cranial MRI examination, with a course of = 3 months, (2) First-time onset, stable vital signs, good cognitive function, MOCA score = 20; (3) The Brunstrom staging of hemiplegic upper and lower limbs is = stage II, and the modified Ashworth scoring scale is = level 2, which can achieve a sitting balance of level 2; (4) Can cooperate with rehabilitation assessment and treatment intervention, and can cooperate with magnetic resonance scanning and near-infrared assessment; (5) This study has been approved by the Hospital Ethics Committee (Approval Number: 2021-08-C005); And all participants signed informed consent forms before the study.

Exclusion criteria

Exclusion criteria: (1) History of severe heart, lung, liver, kidney, and other organ dysfunction, malignant tumors, and mental illness; (2) Conditions that are not suitable for sports training and rehabilitation assessment, such as unhealed fractures, joint dislocations, joint contractures, pain, stiffness, and limited mobility; (3) Wearing a pacemaker, steel plate implantation, intracranial metal implantation, moderate or above cervical instability; (4) Patients who suffer from claustrophobia, auditory hypersensitivity, severe physical weakness, etc., are unable to cooperate with evaluation and treatment, and cannot obtain satisfactory images through magnetic resonance imaging and near-infrared assessment.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment Upper Extremity ;

Secondary

MeasureTime frame
Brain functional connectivity strength;beta;Manual Muscle Testing;Modified Barthel Index;

Countries

China

Contacts

Public ContactXiang Li

The affiliated hospital of jining medical university

791084963@qq.com+86 152 6379 7588

Outcome results

None listed

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