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NOT YET RECRUITING
NCT07600320
NA

Fareon Open Label Device Clinical Trial

Sponsor: Icahn School of Medicine at Mount Sinai

View on ClinicalTrials.gov

Summary

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.

Official title: Microtesla Magnetic Therapy (MMT) Treatment of Cognitive Impairment: Open Label Pilot Study

Key Details

Gender

All

Age Range

16 Years - Any

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2026-05-01

Completion Date

2027-04-30

Last Updated

2026-05-20

Healthy Volunteers

No

Interventions

DEVICE

Fareon device

Participants will use the device 2 times per week for 15 minutes at home.

Locations (1)

The Cohen Center for Recovery from Complex Chronic Illnesses (CoRE)

New York, New York, United States