Fact CheckerSign in

NCT06703320Recruiting

Brain Activation Pattern Caused by Immersive Virtual Reality Pathfinding Task in Stroke Patients: an FNIRS Study

Brain Activation Pattern Caused by Immersive Virtual Reality Pathfinding Task in Stroke Patients: a Functional Near-infrared Spectroscopy Study

Source: ClinicalTrials.gov · Last updated 26 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is an fNIRS study performed to investigate Brain Activation Pattern Caused by Immersive Virtual Reality Pathfinding Task in Stroke Patients.

Status (registry)
Recruiting
Study type
Observational
Enrollment
60 (estimated)
First submitted
21 Nov 2024
Start date
1 Oct 2024
Primary completion date
1 Apr 2025
Lead sponsor
Dingqun Bai
Diseases
Stroke
NCT number
NCT06703320

What you commit to

  • Study type: Observational
  • Planned participants: 60
  • From 1 Oct 2024 to the primary completion date, 1 Apr 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 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

Other

  • Pregnant or lactating women
  • Pregnant or lactating women

Who the study is looking for

  • 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.

Age in the registry: 18 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Department of Rehabilitation Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing,, Chongqing, Chongqing 400010
Coordinator of this site? Confirm its status
ChongqingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.