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Behavioural and Electrophysiological Effects of rTMS in Functional Neurological Disorders

Assessing the Behavioural and Electrophysiological Effects of Repetitive Transcranial Magnetic Stimulation on Intention vs Overt Action in Patients With Functional Neurological Disorders

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04942600
Enrollment
19
Registered
2021-06-28
Start date
2022-01-14
Completion date
2022-07-29
Last updated
2023-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Functional Neurological Disorder

Brief summary

The purpose of this study is to better understand Functional Neurological Disorders (FND) by measuring movement timing and brain activity in patients with FND during deliberate movements and when expressing an 'intention' to move. This investigation will use non-invasive brain stimulation to investigate the role of the temporal-occipital-parietal junction in FND.

Detailed description

This study seeks to improve our neurophysiological understanding of Functional Neurological Disorders (FND) by measuring movement timing and brain activity while individuals with FND perform a simple pointing task. Behavioural (timing of arm and finger movement) and electrophysiological (electroencephalography; EEG) measures will be collected both at rest and while participants perform a voluntary movement task designed to discriminate between brain events related to intention vs. overt action. Furthermore, this study will investigate the ability of a non-invasive brain stimulation technique called repetitive transcranial magnetic stimulation (rTMS) to alter brain activity in the temporal-occipital-parietal junction (TPJ), a region known to be hypo-active in individuals with FND. Tasks and cortical recordings will be repeated following rTMS to determine the effect of brain stimulation on behaviour and brain activity.

Interventions

A non-invasive method of brain stimulation

Sponsors

University of Winnipeg
CollaboratorUNKNOWN
University of Manitoba
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Confirmed diagnosis of Functional Neurological Disorder with motor symptoms.

Exclusion criteria

* Presence of another comorbid psychiatric disorder; * Any contraindication for rTMS (e.g., implanted metal devices; cardiac pacemaker or pacemaker wires; neurostimulators; implanted pumps, metal in the body \[rods, plates, screws, shrapnel, dentures, IUD\] or metallic particles in the body, surgical clips in the head, previous neurosurgery, cochlear implants, prosthetic heart valves); * Currently pregnant.

Design outcomes

Primary

MeasureTime frameDescription
Change in relative timing of intention-to-act vs action production1 hour: Immediately prior to and following one session of rTMSAssessment of change in the lag time between intended and actual action production during pointing and stimulus response tasks.
Change in resting state activity in temporal-parietal junction brain region1 hour: Immediately prior to and following one session of rTMSAssessment of changes in EEG brain activity readings when participants are at rest at various frequencies, primarily targeting delta/theta bands.

Secondary

MeasureTime frameDescription
Change in brain activity related to 'intention to act'1 hour: Immediately prior to and following one session of rTMSAssessment of changes in ERP waveform amplitude related to the 'intention to act' time-stamp during the movement task.
Change in brain activity related to motor production1 hour: Immediately prior to and following one session of rTMSAssessment of changes in ERP waveform amplitude related to the 'motor production' time-stamp during the movement task.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026