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NCT Number: NCT07059325

Accelerated TMS for Seizure-Type Functional Neurologic Disorders

The purpose of this project is to assess the feasibility, tolerability, and preliminary efficacy of using an accelerated, intermittent theta burst stimulation (a-iTBS-rTMS) protocol targeting the left dorsolateral prefrontal cortex (l-dlPFC) for Psychogenic Non-Epileptic Seizures (PNES) or Seizure-Type Functional Neurologic Disorder (FND-seiz) in an open-label fashion. Following screening, consent, and enrollment, participants will receive 6-to-10 iTBS-rTMS sessions per day (i.e., theta burst; 600 pulses per session; 6000 pulses per day) over a 3-to-5 treatment days with a target of 30 total sessions (18,000 total pulses). TMS will be targeted to Beam F3 for comparison to the bulk of the literature and to most mimic replicable and clinical use. This proposed iTBS-rTMS protocol was chosen given its previously shown safety, tolerability, and effectiveness in other conditions, but also as it has the potential to shorten treatment to only 3 days, which investigators theorize will be more feasible for patients with FND-seiz.

Feasibility will be measured as the percentage of participants who receive at least 20 treatment sessions within the 3-to-5-day window. Other than self-assessments used in the safety screening process or to monitor TMS benefits and risks, secondary subjective measures will assess previously investigated FND-seiz-specific outcomes, which will be obtained prior to intervention and 4-weeks post-intervention. In addition to monthly seizure frequency, this will include validated measures regarding stigma, health-related QOL, depression, PTSD, somatic symptoms, psychosocial functioning, psychological distress, and clinical and participant impression of improvement and satisfaction. Sub-analysis will further divide participants with mild to no depression and/or PTSD versus moderate to severe depression and/or PTSD to further assess how the TMS effects known to effect other highly comorbid disorders with FND-seiz, may indirectly affect FND-seiz outcomes.

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Key information

Conditions

Functional Neurological Symptom Disorder Behavior Conversion Disorder Functional Seizures Mental Disorders Nervous System Diseases Neurologic Manifestations Pathological Conditions, Signs and Symptoms Personal Satisfaction Psychogenic Nonepileptic Seizures Psychological Well-Being Seizures Signs and Symptoms Somatoform Disorders

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Institute of Psychiatry, Brain Stimulation Department

Charleston, South Carolina, 29425, United States

Location status: Recruiting

Location contact

Clayton Olash, MD

SUB_INVESTIGATOR

Daniel Alves Neiva Barbosa, MD

SUB_INVESTIGATOR

Joseph A Chasen, DO

CONTACT

[email protected]

8436371358

Joseph A Chasen, DO

PRINCIPAL_INVESTIGATOR

Mark George, MD

SUB_INVESTIGATOR

Mert Bircan, MD

SUB_INVESTIGATOR

Sarah Schmitt, MD

SUB_INVESTIGATOR

About this study

Seizure-Type Functional Neurologic Disorders (FND-seiz) are strikingly prevalent-accounting for 5-15% of epilepsy center referrals and up to 40% of epilepsy monitoring unit admissions-when considering the associated barriers to treatment and dismal outcomes. Due to resource-intensive requirements, diagnosis is often delayed by years. In the interim, patients frequently receive inappropriate antiseizure medications and have high utilization of emergency services. Years after diagnosis, many FND-seiz patients continue to experience non-epileptic seizures (NS) and have high rates of disability. Due to stigma and psychosocial barriers, engagement and responses to the standard of care, Cognitive Behavioral Therapy (CBT), are inconsistent. As many patients are told they may have epilepsy prior to receiving an accurate diagnosis, there is an obvious disconnect between the recommended psychological treatment and the physical nature of their symptoms, which can limit acceptance of the diagnosis and subsequently CBT engagement. Furthermore, the only powered RCT (the CODES trial) examining CBT in FND-seiz failed to show a significant seizure reduction at 12 months follow up and the overall effect size was lower than previously thought highlighting the limitations of a "one-size-fits-all" model for a highly comorbid disorder. Ultimately, patients with FND-seiz have been found to have a poorer overall quality of life compared to epilepsy and a standardized mortality rate 2.5 times greater the general population and comparable to that of drug-resistant epilepsy

Together these factors underscore the need for alternate treatments capable of addressing psychosocial challenges unique to FND-seiz or further investigating the underlying neurobiology. Investigators theorize that offering a brain-network based approach may reduce stigma associated with confusion over the "psychological" rather than "neurological" etiologic conception of FND-seiz, which if effective, may be a more feasible for some patients. Brain-imaging research and prior reports of benefit with neurostimulation suggests TMS to the left dorsolateral prefrontal cortex (l-dlPFC) has the potential to improve cortico-limbic or cortico-sensorimotor governance, which Investigators theorize in FND-seiz may decrease NS frequency or improve quality of life. Thus, Investigators aim to investigate the feasibility and tolerability of an accelerated, intermittent theta-burst TMS protocol in FND-seiz to best mimic current clinical trends and optimize TMS feasibility, which may have several applications for the FND-seiz population.

In clinical practice, the known, but rare risk of inducing an epileptic seizure with TMS and the difficulty differentiating epileptic from non-epileptic seizures, may decrease the comfort of TMS providers to use TMS in FND-seiz patients when indicated for other disabling disorders. In tandem with exploring the feasibility and tolerability of this intervention, Investigators hope to employ and investigate an informed safety protocol, with input from experts in the fields of epilepsy and brain stimulation. Helping providers safely screen patients, more decisively exclude patients with an inaccurate diagnosis or concomitant epilepsy and having a protocol to follow when treating FND-seiz patients who experience a NS during TMS stimulation may increase TMS access for FND-seiz patients with other TMS indications. Finally, as preliminary evidence here at MUSC also suggests combining TMS with CBT for other indications may have a synergistic effect and improve attrition with CBT, if TMS is preliminarily efficacious alone in FND-seiz specific outcomes in a small, open-label sample, this investigation may also help optimize future methodologies examining the use of TMS in FND-seiz.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • >18 years old and <65 years old
  • English Speaking, can read and write, and able to provide informed consent
  • Diagnosis of "documented" Functional Seizures as made by an MUSC epileptologist or neurologist using the ILAE recommendations: "by clinician experienced in diagnosis of seizure disorders (on video or in person), showing semiology of typical of FND-seiz, while on EEG plus no epileptiform activity on routine or ambulatory ictal EEG during a typical ictus/event in which the semiology would make ictal epileptiform EEG activity expected during equivalent epileptic seizures"2
  • In addition to meeting ILAE minimum requirements for FND-seiz diagnosis, must have previously undergone and documented in the electronic medical record a minimum of 24-hours of otherwise normal video EEG without interictal epileptiform findings
  • Duration of symptoms >3 months and continuing to experience NES at least monthly
  • Not currently undergoing any psychotherapeutic intervention, agree to forgo any psychotherapeutic intervention during the study, and if previously completed any psychotherapeutic intervention continue to experience monthly non-epileptic seizures
  • If on psychotropic medications may choose to continue during the duration of the study at current doses, but consent to not modifying medication doses or switching to alternative psychotropic regimens during the trial
  • In good general health, as ascertained by medical history
  • Females of reproductive age (ages 18 to 50) must have a negative urine pregnancy test, performed onsite, and documented in the study record within 72 hours prior to the first TMS session

Exclusion criteria

  • History of clinical concern for concomitant epileptic seizures or epilepsy
  • History of ongoing psychosis, mania, active alcohol or substance use disorder as screened by the PSQ, YMRS, AUDIT, and DAST-10
  • History of positive screening urine test for drugs of abuse within the last year: cocaine, amphetamines, barbiturates, opiates
  • Active suicidal intent or a score >2 on question 3 of the HAM-D
  • Use of medications known to lower the seizure threshold at doses that may increase this risk in the setting of rTMS-iTBS (i.e. buproprion at >300 mg, combinations of tricyclic antidepressants, antipsychotics… as determined by investigators)
  • History of central nervous system surgeries or clinically relevant structural brain lesions
  • Significant or unstable cardiac, metabolic, oncologic, psychiatric, developmental, or neurologic condition(s) or treatments that may impact safe participation in the study as determined by the study investigators (e.g. poorly-controlled heart failure, current or past cardiac arrhythmia, sustained systolic blood pressure >180, labile diabetes, significant electrolyte abnormality, brain cancer, cognitive impairment, neurodevelopmental disorders, autism spectrum disorder, mania, schizophrenia spectrum or other psychotic disorder, movement disorders, multiple sclerosis, moderate to severe brain injury)
  • Participation in any clinical trial with an investigational drug or device within the past month or concurrent to study participation
  • History of TMS exposure
  • TMS contraindications (e.g., ferromagnetic implants, cochlear implants, conditions or treat-ments that lower seizure threshold - as determined by study investigators).
  • Current pregnancy or desire to become pregnant during study duration without contraceptive plan
  • Are a prisoner or in police custody at the time of eligibility screening

Treatment and study plan

Transcranial Magnetic Stimulation

Device

Participants will receive 6 to 10 sessions per day (i.e., theta burst; 600 pulses per session; 6000 pulses per day) over 3 to 5 treatment days using a MagVenture MagPro TMS System. Treatment will consist of a total of 30 sessions (18,000 total pulses). A single session is defined as 600 pulses at 50 Hz for 2s (i.e., 5 Hz triplets) and repeated every 10s for a total of 190s per session to l-dlPFC at 120% rMT with 15-minute intersession intervals. TMS will be targeted to Beam F3 for comparison to the bulk of the literature and to most mimic replicable clinical use.

Other names: Accelerated TMS, Theta-burst TMS

Primary outcomes

  1. Percentage of Participants Completing TMS Sessions

    Time frame: Assessed daily from Day 1 to Day 5 of the TMS treatment period and summarized at the 4-week follow-up visit.

    Description: Feasibility will be measured as the percentage of participants who complete at least 20 rTMS-iTBS treatment sessions within the 3-to-5-day treatment period.

    Unit of Measure: Percentage (%) Time Frame: Assessed daily from Day 1 to Day 5 of the TMS treatment period and summarized at the 4-week follow-up visit.

    Rationale: This measure focuses on the proportion of participants able to adhere to the intensive TMS protocol, a key indicator of feasibility. The time frame is now specific, covering the treatment days (Day 1 to Day 5) and the 4-week follow-up for final reporting.

  2. Session Delivery Patterns

    Time frame: Recorded daily from Day 1 to Day 5 of the TMS treatment period and summarized at the 4-week follow-up visit.

    Description: The number of total rTMS-iTBS sessions delivered will be recorded and analyzed to characterize protocol adherence and delivery patterns. rTMS-iTBS sessions within the protocol are aimed to be delivered over the 3-5 treatment days, during which participants may choose between 6-10 day treatment sessions per day if tolerable and feasible (total of 30 sessions to complete the rTMS-iTBS protocol) Unit of Measure: The number of sessions delivered, represented as a continuous, numerical value.

    Rationale: This measure provides additional detail on how the protocol is implemented, addressing potential variability in session delivery to assess overall tolerability, feasibility, and analyze any potential adverse events. It further helps inform measures of efficacy if participants do not complete the total session target or complete the course of different time periods (ie, over 4-5 days or over 3 days).

  3. Adverse Event Rate

    Time frame: Assessed daily from Day 1 to Day 5 of the TMS treatment period, at the initial screening visit (baseline), and at the 4-week follow-up visit.

    Description: Tolerability will be assessed by calculating the percentage of participants experiencing at least one adverse event (AE) related to the rTMS-iTBS protocol, such as headache, scalp discomfort, or dizziness. Adverse events will be recorded and classified using a standardized checklist based on common TMS-related side effects.

    Unit of Measure: Percentage (%) of participants with at least one AE. Rationale: This measure quantifies the proportion of participants experiencing AEs, providing a clear indicator of the protocol's tolerability. Daily assessments during treatment capture immediate side effects, while the 4-week follow-up evaluates any delayed or persistent effects.

  4. Serious Adverse Event Rate

    Time frame: Assessed daily from Day 1 to Day 5 of the TMS treatment period, at the initial screening visit (baseline), and at the 4-week follow-up visit.

    Description: Serious adverse events (SAEs), defined as any event resulting in hospitalization, life-threatening conditions, or significant disability (e.g., seizure), will be tracked and reported as the percentage of participants experiencing at least one SAE related to the rTMS-iTBS protocol.

    Unit of Measure: Percentage (%) of participants with at least one SAE. Rationale: This measure ensures monitoring of severe outcomes, which is critical for assessing the safety of the TMS protocol. The specific time points align with the study's schedule, ensuring comprehensive tracking of rare but serious events.

  5. Pulses per Session Delivery Patterns

    Time frame: Recorded daily from Day 1 to Day 5 of the TMS treatment period and summarized at the 4-week follow-up visit.

    Description: The number and frequency of rTMS-iTBS pulses delivered over the 3-5 treatment days during which participants may choose between 6-10 day treatment sessions per day. This will be recorded and analyzed to characterize protocol adherence and delivery patterns. A pulse is defined as a burst of three magnetic pulses delivered in quick succession. One treatment session entails 190s encompassing 600 pulses per session. An intermittent theta-burst pulse is defined as a burst of three magnetic pulses delivered in quick succession. The end point of 30 treatment sessions is 18,000 total pulses delivered, which over the 3 to 5 day window can be achieved with 3,600 daily pulses for 5 days or up to 6,000 daily pulses over 3 days.

    Unit of Measure: The number of sessions delivered, represented as a continuous, numerical value.

    Rationale: This measure provides additional detail on how the protocol is implemented, addressing potential variability in session delivery to assess overall tole

Secondary outcomes

  1. Non-epileptic Seizure Frequency (NES)

    Time frame: Assessed prior to intervention at visit 1, 2-4 weeks prior to starting the 3-5 day TMS treatment protocol, and at the final follow up visit 4 weeks after completing the TMS treatment protocol.

    Participants will receive in-person and written documentation on how to document NES frequency (the number NES events over a 4 week period) following events ideally in tandem with a family or support persons who may live with them. The subject and their support person will be asked to document NES semiology, duration, and symptom severity to ensure the events in question are consistent with their known events that have been previously confirmed to represent NES with video EEG. Final analysis will represent a continuous variable comparing the numerical value (number of NES events over a 4 week period).

  2. Chronic Illness Anticipated Stigma Scale (CIASS)

    Time frame: Assessed at initial visit (time point 0 at visit 1, 2-4 weeks pre-TMS) and at post-intervention follow-up (4 weeks post-TMS).

    Purpose: Measures anticipated stigma related to chronic illness in participants with functional seizures.

    Unit of Measure: Total score on a scale. Score Range: 12-60 (12 items, each scored 1-5). Type of Variable: Continuous (sum of item scores). Interpretation: Higher scores indicate greater anticipated stigma (worse outcome).

  3. Montgomery-Asberg Depression Rating Scale (MADRS)

    Time frame: Assessed at initial visit (2-4 weeks pre-TMS) and follow-up (4 weeks post-TMS).

    Purpose: Assesses depression severity in participants with functional seizures. Unit of Measure: Total score on a scale. Score Range: 0-60 (10 items, each scored 0-6). Type of Variable: Continuous (sum of item scores). Interpretation: Higher scores indicate greater depression severity (worse outcome).

    Sub-analysis: Participants divided into mild/no depression (MADRS ≤ 20) vs. moderate/severe depression (MADRS > 20) to compare with FND-seizure-specific outcomes (e.g., NHS3, NES remission).

  4. Post-Traumatic Stress Disorder Checklist for DSM-5 (PCL-5)

    Time frame: Assessed at initial visit (2-4 weeks pre-TMS) and follow-up (4 weeks post-TMS).

    Purpose: Evaluates PTSD symptom severity in participants with functional seizures.

    Unit of Measure: Total score on a scale. Score Range: 0-80 (20 items, each scored 0-4). Type of Variable: Continuous (sum of item scores). Interpretation: Higher scores indicate greater PTSD symptom severity (worse outcome).

    Sub-analysis: Participants divided into mild/no depression (MADRS ≤ 20) vs. moderate/severe depression (MADRS > 20) and absent/mild PTSD (PCL-5 < 33) vs. moderate/extreme PTSD (PCL-5 ≥ 33) to compare with FND-seizure-specific outcomes.

  5. PROMIS®-29+2 Profile v2.1 (PROPr)

    Time frame: Assessed at initial visit (2-4 weeks pre-TMS) and follow-up (4 weeks post-TMS).

    Purpose: Measures health-related quality of life across multiple domains (physical function, anxiety, depression, fatigue, sleep disturbance, social function, pain intensity, pain interference).

    Unit of Measure: T-scores for each domain. Score Range: T-scores (mean = 50, SD = 10) for each domain; typically ranges from 20-80 depending on the domain.

    Type of Variable: Continuous (T-scores per domain).

    Interpretation:

    Physical function and social function: Higher scores indicate better outcomes. Anxiety, depression, fatigue, sleep disturbance, pain intensity, pain interference: Higher scores indicate worse outcomes.

  6. Patient Health Questionnaire-15 (PHQ-15)

    Time frame: Assessed at initial visit (2-4 weeks pre-TMS) and follow-up (4 weeks post-TMS).

    Purpose: Assesses somatic symptom severity in participants with functional seizures.

    Unit of Measure: Total score on a scale. Score Range: 0-30 (15 items, each scored 0-2). Type of Variable: Continuous (sum of item scores). Interpretation: Higher scores indicate greater somatic symptom severity (worse outcome).

  7. Clinical Outcomes in Routine Evaluation (CORE-10)

    Time frame: Assessed at initial visit (2-4 weeks pre-TMS) and follow-up (4 weeks post-TMS).

    Purpose: Measures general psychological distress in participants with functional seizures.

    Unit of Measure: Total score on a scale. Score Range: 0-40 (10 items, each scored 0-4). Type of Variable: Continuous (sum of item scores). Interpretation: Higher scores indicate greater psychological distress (worse outcome).

  8. Clinical Global Impression-Improvement and Severity (CGI-I and CGI-S)

    Time frame: Time Frame: CGI-S assessed at initial visit (2-4 weeks pre-TMS) and follow-up (4 weeks post-TMS); CGI-I assessed only at follow-up (4 weeks post-TMS).

    Purpose: Assesses clinical severity (CGI-S) and improvement (CGI-I) in participants' functional seizure condition.

    Unit of Measure: Rating on a scale.

    Score Range:

    CGI-S: 1-7 (1 = normal, not at all ill; 7 = extremely ill). CGI-I: 1-7 (1 = very much improved; 7 = very much worse). Type of Variable: Ordinal (discrete ratings).

    Interpretation:

    CGI-S: Higher scores indicate greater illness severity (worse outcome). CGI-I: Higher scores indicate less improvement or worsening (worse outcome).

  9. The National Hospital Seizure Severity Scale (NHS3)

    Time frame: Assessed at initial visit (2-4 weeks pre-TMS) and follow-up (4 weeks post-TMS).

    Purpose: Measures seizure severity in participants with functional seizures. Unit of Measure: Total score on a scale. Score Range: 0-27 (based on seizure characteristics, e.g., frequency, duration, injury).

    Type of Variable: Continuous (sum of weighted items). Interpretation: Higher scores indicate greater seizure severity (worse outcome).

  10. Participants with Complete NES Remission

    Time frame: Assessed at follow-up (4 weeks post-TMS).

    Purpose: Determines the proportion of participants achieving complete remission of non-epileptic seizures (NES).

    Unit of Measure: Percentage of participants with no NES events. Score Range: Binary (0% or 100% remission per participant). Type of Variable: Binary (remission achieved or not). Interpretation: Achieving remission (100%) is a better outcome.

  11. Participants with >50% Reduction in NES Frequency

    Time frame: Assessed at follow-up (4 weeks post-TMS).

    Purpose: Measures the proportion of participants with a significant reduction (>50%) in non-epileptic seizure frequency.

    Unit of Measure: Percentage of participants achieving >50% reduction in NES frequency.

    Score Range: Binary (≥50% reduction or <50% reduction per participant). Type of Variable: Binary (reduction achieved or not). Interpretation: Achieving >50% reduction is a better outcome.

Study contacts

Contact information is provided by the study sponsor or research team.

Recruitment Coordinator

CONTACT

[email protected]

(843) 637-1358

Sponsors and collaborators

Lead sponsor

Medical University of South Carolina

Other

Registry information

Official study title

Accelerated, Left Prefrontal Transcranial Magnetic Stimulation for Functional Seizures; An Open-Label Exploration of Feasibility, Tolerability, and Preliminary Efficacy

Acronym: FND-seiz

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Jul 10, 2025
Registry last updated
Sep 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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