Impact of a Biophoton Therapy on Patients With Brain Disorders

Part of paid clinical trials in Butler, Pennsylvania.

Sponsor
First Institute of All Medicines
Study ID
NCT06147999
Status
Recruiting

Conditions

  • Brain Disorders - Alzheimer's Disease, Dementia, Parkinson's Disease, Traumatic Brain Injury

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Biophotonizer - a Biophoton Generator — DEVICE
    A biophotonizer is a device producing strong biophoton field. These biophotons help the human body to gain self-healing capacity to heal many disorders, including brain disorders.

Study Details

Previous clinical studies revealed that the newly developed biophoton therapy has been safe and effective in treating patients with Alzheimer's disease, dementia, stroke, traumatic brain injury, or Parkinson's disease. The current study is to confirm the previous clinical observation by conducting as a randomized, triple-blinded, placebo-controlled prospective intervention clinical research. About 80 patients with brain disorder (Alzheimer's disease, dementia, stroke, traumatic brain injury, Parkinson's disease) will participate in the intervention clinical study at the Tesla MedBed Center located in Butler, PA.

Key Dates

Start date
Nov 8, 2023
Status verified
Aug 2025
Primary completion
Nov 8, 2026
Completion
Nov 8, 2026

Study Design

Enrollment
80 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Treatment Group
    The 14 active Biophoton Generators packed with the same 32-Oz metal can will be labeled with a code and placed under a hotel bed. Each participant will rest on the bed during the entire study period for 4 weeks. Participants will receive biophotons inside of the biophoton field generated by 14 active Biophoton Generators
  • Placebo Comparator: Control Group
    The 14 inactive Biophoton Generators packed with the same 32-Oz metal can will be labeled with a code and placed under a hotel bed. Each participant will rest on the bed during the entire study period for the first 2 weeks. Then will be switched to the active treatment group for being treated for 4 weeks. Participants will receive placebo effect from the 14 inactive comparators.

Primary Outcome Measure

Overall Life Quality impacted by Biophoton Therapy [ Time Frame: 0-2 weeks, 0-4 weeks after starting the study treatment. ]

Locations (1)

FacilityCityStateZIPSite coordinators
Tesla MedBed Center, 139 Pittsburgh Road, Butler, PA 16001ButlerPennsylvania16001
Jessica Jackson, PhD Candidate
3029222486
Audrey Ager
7248101020
Mariola Smotrys, MD, MS, MBA (PRINCIPAL_INVESTIGATOR)
Larry Alpert, MD (SUB_INVESTIGATOR)

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