Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Tuesday, January 6, 2026

Wireless EEG tracks neuroplasticity in trials

 So, we now can exactly identify the signals between neurons that tell one neuron to drop their use and take on a neighboring neuron's use! That could then make neuroplasticity repeatable on demand. If your doctor and hospital aren't pushing for further research on this; THEY ARE COMPLETELY FUCKING INCOMPENT!

Do you prefer your doctor, hospital and board of director's incompetence NOT KNOWING? OR NOT DOING?

Wireless EEG tracks neuroplasticity in trials

Researchers validated a wireless EEG method to measure neuroplasticity, offering a non-invasive way to track how the brain responds to new treatments.

The approach could provide an objective readout of brain response to therapies for psychiatric and neurodegenerative conditions.

Neuroplasticity is the brain’s ability to reorganise its connections after experience, injury or disease, for example by forming new pathways to aid recovery.

The research, conducted by Cumulus Neuroscience, used visual evoked potential (VEP) modulation to mark neuroplasticity.

VEPs are brain signals produced in response to visual patterns.

The method was tested in two US-based clinical trials involving 50 healthy participants.

Brian Murphy, co-founder and chief scientific officer at Cumulus Neuroscience, said: “This study demonstrates that it is possible to measure neuroplasticity reliably in real-world clinical environments using a non-invasive, low-burden, scalable approach.

“Our findings open the door to incorporating objective plasticity measures into early-phase CNS drug development, which could accelerate progress in treating neuropsychiatric and neurodegenerative disorders.”

Conventional EEG assessments are time-consuming and burdensome, which has limited their use in trials.

The new approach uses a quick set-up dry EEG headset with frequency-domain analyses to extract precise measures.

Dr David Walling, chief clinical officer for CenExel-CNS and principal investigator for the study, said: “The ability to capture valid VEPs in clinical studies with easy-to-deploy technology and short sessions has the potential to transform how we assess the efficacy of new therapies in this space.

“Historically, we have not had a way to directly measure neuroplasticity outside of animal models which require invasive techniques.

“We can now integrate non-invasive VEP measures into clinical study workflows, providing sponsors with objective biomarkers of target engagement and treatment effects early in development.”

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