rTMS for Post-COVID Syndrome
Trial Summary
Will I have to stop taking my current medications?
The trial does not specify if you need to stop taking your current medications. However, you must have been stable on psychotropic medications for at least 4 months, and as-needed use of benzodiazepines and beta-blockers is allowed but discouraged during assessment days.
What data supports the effectiveness of the treatment rTMS for Post-COVID Syndrome?
Is repetitive transcranial magnetic stimulation (rTMS) safe for humans?
Repetitive transcranial magnetic stimulation (rTMS) is generally considered safe for humans, with safety guidelines established since 1996 and updated in 2021. While some side effects like headaches and rare cases of seizures have been reported, serious adverse events are uncommon. However, there is a theoretical risk of unintended long-term changes in brain function.678910
How does the treatment rTMS differ from other treatments for Post-COVID Syndrome?
rTMS (Repetitive Transcranial Magnetic Stimulation) is unique because it uses magnetic fields to noninvasively stimulate specific areas of the brain, which can help improve symptoms like depression and anxiety in Long-COVID patients. Unlike other treatments, it directly modulates brain activity and neuroplasticity (the brain's ability to adapt and change), offering a novel approach for managing neuropsychiatric symptoms associated with Post-COVID Syndrome.1231112
What is the purpose of this trial?
This is a pilot randomized trial of rTMS for symptoms of fatigue and brain fog, and other neuropsychiatric symptoms of Long-COVID (Post-COVID, post-acute sequelae of COVID-19 infection, PASC). Twenty participants diagnosed with Long-COVID and recruited from the UCLA Long-COVID clinic will be randomized to receive active rTMS versus sham stimulation for 15 treatments followed by another 15 open-label rTMS treatments. Investigators will compare the safety and tolerability of rTMS vs Sham and examine within-group changes in symptoms of fatigue, sleep, pain, mood, and subjective and objective cognitive impairment. This project will provide information and pilot data for future larger clinical trials.
Research Team
Helen Lavretsky, MD
Principal Investigator
University of California, Los Angeles
Eligibility Criteria
This trial is for individuals with Long-COVID experiencing fatigue, brain fog, and other neuropsychiatric symptoms. Participants will be selected from the UCLA Long-COVID clinic. Specific eligibility criteria are not provided but typically include a confirmed diagnosis of Long-COVID and meeting certain health standards.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive 15 treatments of either active rTMS or sham stimulation, followed by another 15 open-label rTMS treatments
Follow-up
Participants are monitored for safety and effectiveness after treatment
Open-label extension
Participants receive an additional 15 open-label rTMS treatments
Treatment Details
Interventions
- rTMS
rTMS is already approved in United States, European Union for the following indications:
- Obsessive-Compulsive Disorder (OCD)
- Major Depressive Disorder
- Migraines
- Smoking cessation
- Obsessive-Compulsive Disorder (OCD)
- Major Depressive Disorder
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of California, Los Angeles
Lead Sponsor