COMPLETED

Can Patients With Chronic Stroke Regain Living Independence by Daily Energizing With Biophoton Generators

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

Study objective The purpose of this clinical research is to verify if the patient with chronic stroke can regain the ability of living independently after daily using Testa BioHealing® Biophoton Generators to increase the energy of the brain and other parts of the body. Study design This study is a randomized, triple-blinded, placebo-controlled prospective intervention clinical research. At least 46 patients with chronic stroke will participate in the live-in observational study in a Tesla MedBed Center. Study patient population The adult patient with a chronic stroke which was defined as a stroke occurred at least 6 months ago with a significant disability unable to have an independent life, is to be considered as a qualified participant.

Official Title

Can Participants With Chronic Stroke Regain Living Independence by Daily Energizing With a Biophoton Generator

Quick Facts

Study Start:2023-10-31
Study Completion:2024-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06049849

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 to 80 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Must be 18-years or older and can live in a hotel
  2. * Must have a caregiver willing to support the participant's full involvement in the study and can assist to complete all study questionnaires
  3. * Can provide informed consent (maybe assisted by Caregiver)
  4. * Has evidence of a clinical diagnosis of stroke occurred at least 6 months ago.
  5. * Has a disability unable to be living independently per Caregiver
  6. * Can complete all study procedures during the study
  7. * Must be fluent in English (or the Caregiver can fully translate)
  1. * Untreated psychiatric disturbances that would affect trial participation as judged by the Caregiver or by the clinical study medical professional
  2. * Who relies on ventilators
  3. * 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, kidney failure, etc.
  4. * Is participating in another investigational drug or device trial

Contacts and Locations

Study Locations (Sites)

Tesla MedBed Center at Butler-PA
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 Date2023-10-31
Study Completion Date2024-12-31

Study Record Updates

Study Start Date2023-10-31
Study Completion Date2024-12-31

Terms related to this study

Keywords Provided by Researchers

  • stroke, paralysis

Additional Relevant MeSH Terms

  • Chronic Stroke