Function-based Accelerated Stimulation Therapy (FAST-therapy) for Freezing of Gait (FOG) After Parkinson's Disease (PD)

• The proposed research will characterize how inter-individual brain and behavior differences (i.e., gait function behavior and fMRI functional connectivity) at baseline relate to the treatment response.
• This knowledge will provide important information about how interventions can be personalized and optimized.
• The work may increase understanding of the underlying neurobiological mechanisms of neuromodulation for rehabilitation in patients with gait disturbances due to PD.
• Impact: Results will provide insights into the effects of the neuromodulatory treatment on gait and motor dysfunction and could dramatically improve quality of life for patients with PD. The results also will (1) provide a mechanistic foundation for studies of therapeutic iTBS for PD patients, (2) evaluate novel stimulation targets, and (3) markedly condense the duration of treatment into a more manageable timeframe for patients.

Our overall objectives in the current study are to:

• To establish safety, feasibility, and tolerability of a high-dose, resting-state functional connectivity-guided iTBS
• To elucidate the neural mechanism by which such a highly efficient and personalized stimulation approach leads to improvements in freezing of gait in PD.
• To promote rehabilitation neuroscience research that expands current neuromodulatory methods
• To increase understanding of the neurobiological mechanisms underlying such neuromodulatory treatment

The specific aims / hypotheses in the current study are:

• Aim 1: Demonstrate the safety, feasibility and tolerability of high-dose, accelerated, network targeted rTMS in the basal ganglia-cerebellar-motor network.

Working hypothesis: The approach will be safe, feasible and well tolerated by the patients.

• Aim 2: Demonstrate preliminary efficacy of high-dose, accelerated, network-targeted rTMS on freezing of gait.

Working hypothesis: The approach facilitates recovery in motor network dysconnectivity, and thereby will improve FOG after treatment compared to pre-treatment.

• Aim 3: Demonstrate modulation of functional connectivity aftereffects of high-dose, accelerated, network-targeted rTMS.

Working hypothesis: Functional connectivity as assessed with fMRI will change after the high-dose, accelerated, functionally-guided stimulation treatment compared to pre-treatment.

Inclusion criteria

• Parkinson disease (PD) with PD diagnosis based on the recent Movement Disorder Society criteria
• PD subjects >45 years and <90 will be studied
• H&Y2-3 (early PD) subjects will be recruited
• English speaker
• Able to provide written consent prior to admission

Exclusion criteria

• The presence of other neurologic disease or neurologic findings on examination
• Depression: Geriatric Depression Scale (GDS) score >11
• Evidence of a stroke or mass lesion on prior structural brain imaging (CT or MRI)
• Are younger than 45 or older than 90 years old
• Non-English speaker
• Are pregnant, suspect pregnancy or are attempting to become pregnant
• Have a pacemaker, intracardiac lines or any other medically implanted device or medicine pump
• Have cochlear hearing implants
• Are taking GABAergic, NDMA-receptor antagonist, or other drug known to influence neural receptors that facilitate neuroplasticity
• Have non removable body piercings or have foreign objects in body
• Have metal anywhere in the head that could increase a subjects risk of serious injury (not including braces, dental fillings, etc.):

• deep brain or vagus nerve stimulator
• aneurysm clips or coils
• stents in neck or brain
• implanted stimulators
• electrodes to monitor brain activity
• metallic implants in eyes or ears
• shrapnel or bullet fragments in or near the head
• facial tattoos with metallic or magnetic-sensitive ink
• other metal devices or objects implanted in or near the head,
• Have any of the below conditions that would put a subject at increased risk of having a seizure:

• a personal or family history of seizure/epilepsy
• taking prescription drugs that lower the threshold for seizures
• recent history of excessive alcohol consumption
• history of alcohol addiction/dependence
• recent history of recreational drug use
• history of drug addiction/dependence
• Have been diagnosed with any of the following:

• A stroke, brain hemorrhage, brain tumor, encephalitis, or multiple sclerosis
• Alzheimer's disease
• attention deficit disorder, schizophrenia, or manic depressive (bipolar) disorder
• normal pressure hydrocephalus or increased intra-cranial pressure
• diabetes requiring insulin treatment
• any serious heart disorder or liver disease

• Metallic medical implants (i.e. pacemaker), foreign objects in body, non-removable body-piercings 7. Pregnancy 8. Additional exclusion criteria related to TMS: g. Metal in the cranium (mouth excluded) h. Cardiac pacemaker i. Implanted medication pump j. Implanted deep brain stimulator or vagus nerve stimulator k. Intracardiac lines l. Serious heart disease m. Increased intracranial pressure n. History of seizures o. Epileptogenic medication p. Cochlear implants q. Recent extended air travel resulting in jetlag or other sleep deprived state