Skip to content

Research on vestibulo-cortical pathway for vestibular rehabilitation to improve spatial cognitive function in stroke

Research on vestibulo-cortical pathway for vestibular rehabilitation to improve spatial cognitive function in stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087857
Enrollment
Unknown
Registered
2024-08-06
Start date
2024-08-08
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

stroke

Interventions

Control group:None
Group with vestibular symptoms and cognitive impairment:Vestibular rehabilitation
Group with vestibular symptoms but no cognitive impairment:Vestibular rehabilitation

Sponsors

Tianjin Huanhu Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients meeting the diagnostic criteria for stroke, confirmed as cerebral infarction by head MRI, and experiencing their first stroke. 2.Patients meeting the diagnostic criteria for vestibular symptoms as defined by the International Classification of Vestibular Disorders 3.Patients aged between 18 and 80 years. 4.Disease duration of 1to 3 months. 5.A score of =3 on the Functional Ambulation Category (FAC) scale. Patients able to walk independently for 10 meters without assistance and maintain this for 15 minutes. 6.Approval from the hospital's medical ethics committee to conduct this study

Exclusion criteria

Exclusion criteria: 1.Patients with multiple lesion strokes confirmed by imaging (head MRA, CTA, or DSA), or those with stroke in the internal carotid artery system supply area, severe stenosis of large vessels, or arterial dissection 2,Patients with reduced peripheral vestibular function or hearing loss. 3,The patient has recurrent stroke, hearing loss, tumor, vascular malformation and severe white matter hyperintensity (periventricular and deep white matter hyperintensity Fazekas grade > 1), anxiety and depression. 4,Patients unable to complete the test due to cognitive impairments, unilateral neglect, or aphasia. Approval from the hospital's medical ethics committee to conduct this study

Design outcomes

Primary

MeasureTime frame
Cognitive function;Imaging indicators;

Secondary

MeasureTime frame
Vestibular function;

Countries

China

Contacts

Public ContactYin Miaomiao

No.6 Jizhao Road, Jinnan District, Tianjin

yinmiao198801@163.com+86 22 5906 5601

Outcome results

None listed

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