Actively Recruiting
Brain-Computer Interface With Virtual Reality in Upper Limb Rehabilitation After Stroke A Randomized Crossover Trial
Led by Technical University of Lisbon · Updated on 2026-02-03
12
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
T
Technical University of Lisbon
Lead Sponsor
C
Centro de Medicina de Reabilitação de Alcoitão
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to evaluate whether motor imagery training combined with brain-computer interface BCI and virtual reality VR can improve arm and hand recovery after stroke. The trial focuses on understanding if adding immersive VR to BCI training enhances upper limb movement, daily activity performance, and brain activity related to movement. Researchers will compare this combined approach to standard motor imagery with BCI to assess any added benefits for stroke survivors. Participants will undergo two separate intervention periods in random order one involving motor imagery-based BCI training with immersive VR and multimodal feedback, and the other using motor imagery-based BCI with a cue-based visual protocol. Each intervention consists of three weekly sessions over six weeks, with a three-week gap between periods. Both training types use EEG-based BCI control, while the VR sessions involve an immersive headset and haptic controllers providing visual, auditory, and touch feedback. During the study, participants will complete four assessment sessionsbefore and after each intervention periodto measure changes in upper limb motor function and activity using clinical tests. Brain activity will be monitored through EEG during all intervention sessions to assess neural changes. The total study duration for each participant is up to 15 weeks, including both interventions and the washout period. Researchers will also explore participant experiences and individual factors influencing outcomes.
CONDITIONS
Brief Title
BCI With Virtual Reality for Stroke Rehabilitation: A Crossover Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Clinical diagnosis of stroke confirmed by neuroimaging with resulting upper limb hemiparesis
- Time since stroke between 6 and 24 months at selection
- Sufficient cognitive ability to understand and follow intervention procedures
- Spasticity score less than 3 on the Modified Ashworth Scale in upper limb muscles
- Adults aged 18 to 80 years
- Ability to remain seated for about 2 hours
- Motivation to participate and capacity to provide informed consent
- Undergoing conventional rehabilitation therapy during the study period
You will not qualify if you...
- Severe communication difficulties preventing comprehension or execution of instructions
- Skin lesions, allergies, metal implants in the head area, or history of craniectomy that hinder electrode placement or EEG signal acquisition
- Other neurological or musculoskeletal conditions affecting upper limb motor function
- Other neurological, musculoskeletal, or psychiatric conditions that may affect participation or study outcomes (e.g., major depression, severe visual impairment, photosensitive epilepsy, frequent vertigo)
- Upper limb impairment caused by a previous stroke separate from the current one
Research Team
A
Athanasios Vourvopoulos, PhD
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