Transcranial Magnetic Stimulation in Misophonia
- Conditions
- Misophonia
- Registration Number
- NCT06960083
- Lead Sponsor
- Icahn School of Medicine at Mount Sinai
- Brief Summary
The purpose of the project is to assess the efficacy of parietal transcranial magnetic stimulation in misophonia. N=60 participants will undergo two transcranial magnetic stimulation sessions: one inhibitory and another excitatory. During both sessions, the parietal region will be stimulated. Participants will perform computerized tasks immediately before and after the stimulation, while EEG, heart rate, and skin temperature will be recorded. These recordings will be used to assess if TMS can be used to improve tolerance to misophonia triggers.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 60
- Hypersensitive to presence of a specific sound, which may be accompanied by irritation, anger/outbursts, or fear.
- Must be between the ages of 18 - 55.
- Must be fluent in English since the study's instructions, surveys, and tasks will be in English.
- Axis I Psychiatric condition, past or present, as defined in DSM-V.
- Disability or medical condition that prohibits completion of study. Participants must be able to complete all study procedures to ensure optimal conditions for data analysis.
- Central Nervous System (CNS) disease, such as history of brain abnormalities (e.g., neoplasms, subarachnoid cysts), cerebrovascular disease, infectious disease (e.g., abscess), or other neurological diseases, history of head trauma (defined as loss of consciousness>3 min), or history of seizures without a resolved etiology. CNS disease and drugs that act in the peripheral or central nervous system are likely to have effects on patterns of neural activity.
- Recent or regular use of psychotropic medication (e.g., amitriptyline for migraines).
- Recent use of drugs of abuse.
- Presence of any mental implants in the head.
- Pregnant or lactating.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Primary Outcome Measures
Name Time Method Unpleasantness Rating Scale after each session, 72 hours apart (each session is 2 hours) Participants will be presented with a slider with extremes labelled as extremely unpleasant and extremely pleasant. Ratings will be provided for audio clips and visual cues. Full scale from 0-100, higher score indicates more unpleasantness
- Secondary Outcome Measures
Name Time Method Heart Rate after each session, 72 hours apart (each session is 2 hours) The heart rate (number of beats per minute) will be measured using a wristwatch worn by the participant.
Skin Conductance Response after each session, 72 hours apart (each session is 2 hours) Skin conductance, a measure capturing the amount of sweat, will be measured using a wristwatch worn by the participant.
EEG P1-N1-P2 Complex Peak Amplitude after each session, 72 hours apart (each session is 2 hours) Amplitude (microvolts) of P1, N1, and P2 peaks measured in the parietal region
EEG P1-N1-P2 Complex Peak Latency after each session, 72 hours apart (each session is 2 hours) Latency (milliseconds) of P1, N1, and P2 peaks measured in the parietal region
EEG Frequency Band Amplitude after each session, 72 hours apart (each session is 2 hours) Amplitude (decibel) in theta (4-8 Hz), alpha (8-13 Hz), and beta (13-30 Hz) frequency bands in the parietal region
EEG Frequency Band Inter-Trial Coherence after each session, 72 hours apart (each session is 2 hours) Coherence (unitless) across trials in theta (4-8 Hz), alpha (8-13 Hz), and beta (13-30 Hz) frequency bands in the parietal region
Trial Locations
- Locations (1)
Mount Sinai West
🇺🇸New York, New York, United States
Mount Sinai West🇺🇸New York, New York, United StatesDaniela Schiller, PhDContactdaniela.schiller@mssm.eduMartijn Figee, MD, PhDContactmartijn.figee@mssm.eduParul JainPrincipal Investigator