Assessing the Behavioural and Electrophysiological Effects of Repetitive Transcranial Magnetic Stimulation on "Intention" vs "Overt Action" in Patients With Functional Neurological Disorders
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Functional Neurological Disorder
- Sponsor
- University of Manitoba
- Enrollment
- 19
- Locations
- 1
- Primary Endpoint
- Change in relative timing of intention-to-act vs action production
- Status
- Completed
- Last Updated
- 3 years ago
Overview
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.
Investigators
Eligibility Criteria
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.
Outcomes
Primary Outcomes
Change in relative timing of intention-to-act vs action production
Time Frame: 1 hour: Immediately prior to and following one session of rTMS
Assessment 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 region
Time Frame: 1 hour: Immediately prior to and following one session of rTMS
Assessment of changes in EEG brain activity readings when participants are at rest at various frequencies, primarily targeting delta/theta bands.
Secondary Outcomes
- Change in brain activity related to 'intention to act'(1 hour: Immediately prior to and following one session of rTMS)
- Change in brain activity related to motor production(1 hour: Immediately prior to and following one session of rTMS)