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Effects and related products development of Synchronized VR Action Observation and FES on Motor Function of Patients with Stroke base on Mirror Neruon System

Effects and related products development of Synchronized VR Action Observation and FES on Motor Function of Patients with Stroke base on Mirror Neruon System

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063552
Enrollment
Unknown
Registered
2022-09-10
Start date
2022-09-10
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

stroke

Interventions

experiment group:During the treatment of FES, the VR movements related to the stimulated muscles were observed synchronously.
control group:Watch irrelevant videos (such as scenery, etc.) while receiving FES treatment.

Sponsors

China Rehabilitation Research Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: 1. Stroke patients, including cerebral infarction and cerebral hemorrhage, meet the stroke diagnostic criteria established by the fourth National Conference on Cerebrovascular Diseases in 1995; 2. Confirmed as stroke by CT or MRI; 3. Unilateral limb hemiplegia; 4. Brunnstrom grade II~IV; 5. Right-handed, determined by the Edinburgh dominant hand Survey (Edinburgh Handedness Inventory, EHI); 6. Adults, aged 30-70 years old. 7. Subacute stage, the course of the disease is 3 to 6 months; 8. First onset; 9. Mini-Mental State scale (Mini-Mental State Examination, MMSE) score >= 27, able to carry out treatment instructions, without severe cognitive and speech impairment, able to understand passwords and communicate with therapists; 10. Without visual impairment, the international standard visual acuity chart checks binocular vision or corrected vision >= 1.0; 11. The vital signs are stable, the disease is no longer progressing, and can tolerate 30 minutes of treatment per day; 12. Junior high school education or above.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1. Subarachnoid hemorrhage, venous sinus thrombosis, transient ischemic attack, progressive stroke, or reversible cerebral ischemia; 2. Lesions located in bilateral cerebral hemispheres, cerebellum, or brainstem; 3. There are contraindications for FES treatment: skin injuries or skin diseases (such as eczema), acute infections (such as osteomyelitis), vascular diseases (such as thrombosis or phlebitis), metal implants and pacemakers, etc.; 4. Complicated with other major diseases, such as heart, lung, liver, kidney, and other organ diseases or failure; 5. Age < 29 years; 6. Non-first onset; 7. Surgery and other invasive treatment; 8. Other clinical problems that affect the evaluation results, such as poor vision, recent or unhealed fractures, vestibular diseases; 9. Other neurological diseases, such as multiple sclerosis, Parkinson's disease, etc.; 10. There are serious mental and psychological problems.

Design outcomes

Primary

MeasureTime frame
Functional Near-Infrared Spectroscopy, fNIRS;

Secondary

MeasureTime frame
Surface electromyography, sEMG;rehabilitation assessment scales;

Countries

China

Contacts

Public ContactCui Yao
xyysfwdm@163.com+86 10 87569178

Outcome results

None listed

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