Fareon Device for Cognitive Impairment
What You Need to Know Before You Apply
What is the purpose of this trial?
The purpose of this study is to assess the safety and feasibility of an at-home MMT treatment in patients with cognitive dysfunction related to acquired brain injury, Long COVID, traumatic brain injury, myalgic encephalomyelitis (ME/CFS), and other neurodegenerative diagnoses including but not limited to Alzheimer's disease and to collect data on safety and efficacy to inform the design of larger clinical studies.
Who Is on the Research Team?
David Putrino, PhD
Principal Investigator
Icahn School of Medicine at Mount Sinai
Are You a Good Fit for This Trial?
This trial is for people aged 16 or older who speak English and have mild memory or thinking problems linked to conditions like brain injury, Long COVID, chronic fatigue syndrome (ME/CFS), or Alzheimer's. Participants must be able to consent (or have a guardian do so) and attend study visits online or in person.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants undergo at-home MMT treatment for cognitive dysfunction
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Fareon device
Trial Overview
The study tests the safety and practicality of using the Fareon device—a home-based treatment—for people with cognitive issues from various brain-related conditions. Researchers will monitor how safe it is and gather early data on its effects.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Participants with cognitive dysfunction related to acquired brain injury, Long COVID, traumatic brain injury, myalgic encephalomyelitis (ME/CFS), and other neurodegenerative diagnoses including but not limited to Alzheimer's disease
Find a Clinic Near You
Who Is Running the Clinical Trial?
Icahn School of Medicine at Mount Sinai
Lead Sponsor
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