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Virtual reality technology improves the upper limbs of stroke patients Dysfunction efficacy study: randomized controlled trials

Virtual reality technology improves the upper limbs of stroke patients Dysfunction efficacy study: randomized controlled trials

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300079269
Enrollment
Unknown
Registered
2023-12-28
Start date
2023-12-30
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

CVA

Interventions

control group:Routine rehabilitation treatment (manipulation, intermediate frequency, acupuncture and moxibustion, etc.).
Experimental group:Routine rehabilitation treatment (manipulation, intermediate frequency, acupuncture and moxibustion, etc.) + virtual reality training

Sponsors

Northern Jiangsu People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Conforming to the diagnostic criteria for stroke in the 2018 Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke or the 2019 Chinese Guidelines for the Diagnosis and Treatment of Cerebral Hemorrhage, confirmed by CT or MRI; (2) Age range from 30 to 65 years old; (3) The first occurrence of unilateral ischemic or hemorrhagic stroke, with a course of>2 weeks and<3 months; (4) Stable vital signs; (5) Good cognitive function, MMSE assessment shows no cognitive impairment, and can cooperate with treatment; (6) Being able to maintain a sitting position independently for at least 30 minutes; (7) No auditory or visual impairment; (8) The affected upper limb can engage in passive movement, with an improved Ashworth score of<3 levels; (9) Can provide written informed consent.

Exclusion criteria

Exclusion criteria: (1) Not the first occurrence of unilateral ischemic or hemorrhagic stroke; (2) Unstable vital signs, such as unstable blood pressure, angina, etc; (3) Upper limb musculoskeletal injuries such as shoulder periarthritis, rotator cuff injury, or upper limb fractures; (4) Other neurological disorders: Parkinson's disease, cervical spondylotic radiculopathy, or nerve compression disorders such as carpal tunnel syndrome; (5) Having a history of epilepsy, brain injury outside of stroke, and skull defects; (6) Have a history of mental illness.

Design outcomes

Primary

MeasureTime frame
Upper limb Fugl Meyer motor function assessment;

Secondary

MeasureTime frame
modified Barthel index;manual muscle test;Improved Ashworth muscle tone assessment;visual analogue scale;

Countries

China

Contacts

Public ContactZhaoxiang Meng

Northern Jiangsu People's Hospital

yzmzx001@163.com+86 189 5257 8698

Outcome results

None listed

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