Alzheimer’s Vielight 810 and Neuro Red Light Doses

Weeks 1-2, 14.2 mW/cm^2 per nostril (2); Weeks 2-12, 41 mW/cm^2 per transcranial target (4); 23 mW/cm^2 per nostrial (2)

Weeks 1-2

  • “810” Intranasal Vielight Device
    • intranasal targets  (2)
    • 810 nm pulsed at 10 Hz
    • 14.2 mW/cm^2 per nostril
    • 25 min.
    • 10.65 J/cm^2 per nostril

Weeks 3-12

  • “Neuro” Transcranial and Intranasal Vielight Device
    • transcranial targets (4)
      • 810 nm pulsed at 10 Hz
      • 41 mW/cm^2 per target
      • 25 min.
      • 24.6 J/cm^2 per target
    • intransal targets (2)
      • 810 nm pulsed at 10 Hz
      • 23 mW/cm^2 per target
      • 25 min.
      • 13.8 J/cm^2 per target

 

 

 

810 nm 10 Hz pulsed, transcranial and intranasal treating cortical nodes of

bilateral mesial prefrontal cortex, precuneus/posterior cingulate cortex, angular gyrus, and hippocampus

12 weeks

MMSE and Alzheimer’s Disease Assessment Scale

intranasal 1x/day/12 week  (84); transcranial 1x/week/12 weeks (12)

Materials and methods: The study used 810 nm, 10 Hz pulsed, light-emitting diode devices combining transcranial plus intranasal PBM to treat the cortical nodes of the DMN (bilateral mesial prefrontal cortex, precuneus/posterior cingulate cortex, angular gyrus, and hippocampus). Five patients with mild to moderately severe cognitive impairment were entered into 12 weeks of active treatment as well as a follow-up no-treatment, 4-week period. Patients were assessed with the MMSE and Alzheimer’s Disease Assessment Scale (ADAS-cog) tests. The protocol involved weekly, in-clinic use of a transcranial-intranasal PBM device; and daily at-home use of an intranasal-only device.

Vielight improves Alzheimer patients sleep, emotion, and wandering.

Results: There was significant improvement after 12 weeks of PBM (MMSE, p < 0.003; ADAS-cog, p < 0.023). Increased function, better sleep, fewer angry outbursts, less anxiety, and wandering were reported post-PBM. There were no negative side effects. Precipitous declines were observed during the follow-up no-treatment, 4-week period. This is the first completed PBM case series to report significant, cognitive improvement in mild to moderately severe dementia and possible AD cases.

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