Safety and Efficacy of Multisensory Stimulation Virtual Reality for Stroke Patients.
Recruiting now · Not applicable
Conditions studied: Stroke
In brief
This was a single-blind randomized controlled trial of multisensory stimulation virtual reality to improve motor and cognitive dysfunction in stroke patients.
Key facts
- Study ID
- NCT06275516
- Run by
- First Affiliated Hospital of Chongqing Medical University
- People needed
- 40
- Starts
- 2024-03-20
- Expected to finish
- 2026-07-30
- Last updated by the study team
- 2026-03-19
Who can join
Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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 may not qualify if…
- 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.
Where it is running
- The First Affiliated Hospital of Chongqing Medical University, First Branch — Chongqing, Chongqing Municipality, China (enrolling)
Full record on ClinicalTrials.gov
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