Actively Recruiting
Safety and Efficacy of Multisensory Stimulation Virtual Reality for Stroke Patients.
Led by First Affiliated Hospital of Chongqing Medical University · Updated on 2026-03-19
40
Participants Needed
1
Research Sites
123 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This was a single-blind randomized controlled trial of multisensory stimulation virtual reality to improve motor and cognitive dysfunction in stroke patients.
CONDITIONS
Official Title
Safety and Efficacy of Multisensory Stimulation Virtual Reality for Stroke Patients.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- The first onset of stroke is diagnosed and confirmed according to the requirements of stroke
- The Fugl-Meyer Assessment of Lower Extremity (FMA-LE) is less than 34.
- 18-85 years of age.
- Able to walk with minor assistance
- MMSE score of 20-30 and ability to understand and follow instructions during the trial
- Able to sign an informed consent form.
You will not qualify if you...
- Severe visual or hearing impairments.
- Pregnant or breastfeeding women.
- Patients with unrepaired cranial bone flaps or metallic implants following brain surgery.
- Presence of other conditions affecting lower limb motor function, such as osteoarthritis or recent lower limb fractures.
- History of severe psychiatric disorders, other neurological diseases, acute cardiopulmonary dysfunction, multiple organ failure, brain tumours, or epilepsy.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The First Affiliated Hospital of Chongqing Medical University, First Branch
Chongqing, Chongqing Municipality, China, 400016
Actively Recruiting
Research Team
D
Dingqun Bai
CONTACT
Z
Zheng Yang
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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