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Research on the Effect of Multimodal VR Intelligent Rehabilitation Technology on the Comprehensive Function of Stroke Limbs and Brain Function

Research on the Effect of Multimodal VR Intelligent Rehabilitation Technology on the Comprehensive Function of Stroke Limbs and Brain Function

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082284
Enrollment
Unknown
Registered
2024-03-26
Start date
2022-11-30
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

stroke

Interventions

VR group:VR treatment, based on conventional physical therapy
Conventional physical therapy group:Routine physical therapy, wearing VR glasses to watch training videos of the same duration

Sponsors

Ningbo Rehabilitation Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: The clinical symptoms and imaging diagnosis are consistent, and the initial intervention is unilateral limb comprehensive dysfunction within 12 months after the first onset; No other neurological complications, no history of critical illness, and no history of blood transfusion during prevention; 35 to 70 years old, with a primary school education or above; Good follow-up compliance and assistance in examination cooperation; Complete hearing, vision, and speech functions.

Exclusion criteria

Exclusion criteria: 1. Previous history of stroke, or accompanied by a history of epilepsy or mental disorders 2. Patients with severe visual impairment or visual perception impairment, including otolith, Meniere's syndrome, long-term migraine, and other unsuitable VR devices 3. Difficulty in changing body position and severe impairment of cardiopulmonary function 4. Hand muscle spasms or wrist or finger deformities (Ashworth>Level 2) 5. Complicated regional pain syndrome or severe pain (VAS>7 points), recent fractures, severe lower limb venous thrombosis 6. History of neuropathy caused by confirmed diabetes or other types (relevant peripheral neuropathy is excluded by EMG) 7. Failure to obtain sufficient understanding and informed consent Any one of the exclusion criteria mentioned above cannot be included in this study

Design outcomes

Primary

MeasureTime frame
Brunnstrom score;

Secondary

MeasureTime frame
Berg balance scale;Holden walking function score; MMSE score;modified Barthel index score; NIHSS score;HAMD-17 item score;Wada drinking water test;MAS score;VAS score;

Countries

China

Contacts

Public ContactMin Tang

Ningbo Rehabilitation Hospital

2398493251@qq.com+86 138 5822 1085

Outcome results

None listed

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