Brain activity during a virtual reality pathfinding task in stroke patients
Measures brain activity during a virtual reality navigation task in adults with stroke.
Plain-language title generated from the registry record
Registry title: Brain Activation Pattern Caused by Immersive Virtual Reality Pathfinding Task in Stroke Patients: an FNIRS Study
Key facts
- Where
- Chongqing, ChinaSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 80 years old?
Source: NCT06703320, who can take part
Where in China
- Department of Rehabilitation Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing,, Chongqing, Chongqing 400010Chongqing, ChinaTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Dingqun Bai
- Trial code
- NCT06703320
- Record updated
- 26 November 2024
- Original description
This is an fNIRS study performed to investigate Brain Activation Pattern Caused by Immersive Virtual Reality Pathfinding Task in Stroke Patients.Read full original descriptionShow less
Brain Activation Pattern Caused by Immersive Virtual Reality Pathfinding Task in Stroke Patients: a Functional Near-infrared Spectroscopy Study
This is an fNIRS study performed to investigate Brain Activation Pattern Caused by Immersive Virtual Reality Pathfinding Task in Stroke Patients.
Inclusion: Stroke patients:; Diagnosis of stroke confirmed by neuroimaging (CT or MRI); 18-80 years old; Able to complete the cognitive task; Able to follow instructions to complete the trial; Patients who signed an informed consent form; Healthy Subjects:; No abnormalities on cranial; 18-80 years old; Able to complete cognitive task; Able to follow instructions to complete the trial; not taking medications; Subjects who signed an informed consent form.
Exclusion: Stroke patients:; Inability to tolerate the test due to organic diseases; Serious mental illness that prevents them from cooperating with or tolerating the trial; Had metal implants, a history of other neurological disorders, acute cardiopulmonary dysfunction; Healthy Subjects:; Inability to tolerate the test due to organic diseases; Serious mental illness that prevents them from cooperating with or tolerating the trial; Had metal implants, a history of other neurological disorders, acute cardiopulmonary dysfunction; Pregnant or lactating women; Pregnant or lactating women.