RECRUITING

Impact of a Biophoton Therapy on Patients With Brain Disorders

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Impact of a Biophoton Therapy on Patients With Brain Disorders

Quick Facts

Study Start:2023-11-08
Study Completion:2024-11-22
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06147999

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Must meet conditions for approval.
  2. * Must be 18-years or older and stay in a hotel.
  3. * Must have a caregiver willing to support the participant's full involvement in the study. • The caregiver can assist in completing all study surveys.
  4. * Can provide informed consent or can be assisted by caregiver.
  5. * Can provide a clinical diagnosis of a brain disorder.
  6. * Can complete all study procedures during the study.
  7. * Must be fluent in English (or the Caregiver can fully translate).
  8. * Women of childbearing age must provide results of a pregnancy test in order to participate.
  1. * Any untreated mental illnesses, that would affect study participation. This will be judged by the caregiver, or by the clinical study medical expert.
  2. * Someone that relies on a ventilator.
  3. * Someone who has a deep brain stimulator, pacemaker, or any implanted electronic devices.
  4. * Co-morbid conditions that would interfere with study activities or response to treatment, which may include severe chronic pulmonary disease, history of uncontrolled seizures, acute or chronic infectious illness, severe diabetes, kidney failure, or any end-of-life prognosis.
  5. * Is participating in another investigational drug or device trial.
  6. * Has an active infectious disease, such as COVID-19.
  7. * Pregnant women.

Contacts and Locations

Study Locations (Sites)

Tesla MedBed Center, 139 Pittsburgh Road, Butler, PA 16001
Butler, Pennsylvania, 16001
United States

Collaborators and Investigators

Sponsor: First Institute of All Medicines

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-11-08
Study Completion Date2024-11-22

Study Record Updates

Study Start Date2023-11-08
Study Completion Date2024-11-22

Terms related to this study

Keywords Provided by Researchers

  • Alzheimer's Disease, and/or
  • dementia, and/or
  • Parkinson's Disease, and/or
  • Traumatic Brain Injury, and/or

Additional Relevant MeSH Terms

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