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.

Saturday, August 22, 2026

A specific transcranial near-infrared stimulation parameter combination targeting the motor cortex improves cortical excitability and hemodynamics

 Ask your competent? doctor; DOES THIS IMPROVE STROKE RECOVERY?  Not nebulous excitability which means nothing to survivors! Oh NO, your doctor doesn't know about this and doesn't care to find out! Get that doctor fired for incompetence, not following research!

A specific transcranial near-infrared stimulation parameter combination targeting the motor cortex improves cortical excitability and hemodynamics

    We’re sharing this article early to provide faster access to peer-reviewed, accepted research. It is citable and carries a permanent DOI. This version is subject to further edits and will be replaced automatically by the final Version of Record. All legal disclaimers apply.

    Abstract

    Background

    Transcranial near-infrared stimulation (tNIRS) is an emerging, light-based, non-invasive neuromodulation technique with great potential to improve functions like cognition and motor performance. Cortical excitability and hemodynamic changes represent key neurophysiological mechanisms of tNIRS effects. The selection of tNIRS parameters is closely associated with their functional effects, and the neurophysiological alterations induced in the human cerebral cortex by different parameter combinations warrant further exploration.

    Methods

    Twenty-two healthy participants received four types of active tNIRS and a Sham condition of tNIRS over the left motor cortex in a randomized order, which included five stimulus conditions: Sham, 810-nm continuous wave (CW), 810-nm 40-Hz pulsed wave (PW), 1064-nm CW, and 1064-nm 40-Hz PW. Each session was divided into three phases, namely pre-stimulation, stimulation, and post-stimulation. Changes in cortical excitability were assessed by recording motor evoked potentials (MEPs) before and for up to 30 min after stimulation. Concurrently, behavioral performance and cortical hemodynamic changes induced by tNIRS were evaluated using functional near-infrared spectroscopy (fNIRS) during a finger-opposition task.

    Results

    Compared to the Sham condition, all active tNIRS protocols induced an increase in MEPs recorded from the right abductor pollicis brevis muscle. At 30 min post-stimulation, the 1064-nm 40-Hz PW condition elicited significantly larger MEP amplitudes than both the 810-nm CW and 1064-nm CW conditions. For behavior, the number of completed cycles during the right-hand finger-opposition task was significantly higher in the 1064-nm 40-Hz PW condition compared to the Sham condition. Regarding cortical hemodynamics, the 1064-nm 40-Hz PW condition showed decreased activation in broad regions of the frontal and motor cortices during the left-hand finger-opposition task compared to baseline. Conversely, the 810-nm 40-Hz PW condition exhibited decreased hemodynamic activation only in the motor cortex during the right-hand finger-opposition task.

    Conclusion

    The 40 Hz pulsed tNIRS protocol with a wavelength of 1064 nm, irradiance of 120 mW/cm2, duration of 20 min, and stimulation area of 0.24 cm2 induced more pronounced changes in cortical excitability and hemodynamics. This enhanced effect may be attributed to the more significant neurophysiological cumulative response elicited by this specific parameter combination. This specific parameter set represents a promising candidate for future clinical applications of tNIRS.

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