Exercise and Transcranial Magnetic Stimulation: Increasing Brain Plasticity in Parkinson's Disease
Launched by NYU LANGONE HEALTH · Apr 13, 2016
Trial Information
Current as of June 29, 2025
Completed
Keywords
ClinConnect Summary
Twenty-four PD patients (n=24) will be randomly assigned to receive one of two interventions for a duration of two weeks. In Group 1, subjects will participate in daily sessions of sham-rTMS followed by supervised aerobic exercise (Sham rTMS+Aerobic); in Group 2, subjects will participate in a combination of rTMS and supervised aerobic exercise (Real rTMS+Aerobic). Serum BDNF-TrkB signaling in lymphocytes and TMS-based electrophysiological measures of LTP-like plasticity will be measured. A comparison of such measures in a group of patients with PD and in a group of age-matched controls (n=...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Diagnosis of PD according to the UK Brain Bank Criteria, confirmed by a neurologist with expertise in movement disorders;
- • Hoehn and Yahr stage II to III;
- • On a stable medication regimen since at least 2 weeks prior the enrolment in the study and, in the view of the treating neurologist, unlikely to require medication adjustments in the following 3-6 months.
- • Inclusion Criteria (Healthy Controls)
- • Male or Female; aged 35-85
- • Exclusion Criteria (Healthy Controls)
- • History of seizure disorder, including febrile seizures;
- • Neurological disorder including PD, stroke, traumatic brain injury, fainting spells or syncope of unknown cause(s);
- • Major or unstable medical illness;
- • Pacemakers, neurostimulators, tattoos or metal foreign bodies in the head area (dental fillings are allowed);
- • Untreated depression, or score of \>20 on Beck Depression Inventory II;
- • Taking any of the following medications within the six weeks prior to the start of the study: imipramine, amitriptyline, doxepin, nortriptyline, maprotiline, chlorpromazine, clozapine, foscarnet, ganciclovir, ritonavir, theophylline, calcium channel blockers, beta blockers, tadalafil, vardenafil, avanafil, and sildenafil;
- • Diagnosis of dementia, or Montreal Cognitive Assessment (MoCA) \<20;
- • Any clinically significant abnormality on vital signs
- • Cardiopulmonary limitations: untreated high blood pressure, history of heart insufficiency (class II-III), coronary vascular disease, angina, arrhythmia, dyspnea on exertion and asthma
About Nyu Langone Health
NYU Langone Health is a premier academic medical center located in New York City, renowned for its commitment to advancing healthcare through innovative research and clinical excellence. As a leading sponsor of clinical trials, NYU Langone Health integrates cutting-edge scientific inquiry with patient-centered care, striving to develop new therapies and improve health outcomes across a wide range of medical conditions. The institution is dedicated to fostering collaboration among researchers, clinicians, and patients, ensuring rigorous adherence to ethical standards and regulatory guidelines in all clinical research initiatives. By leveraging its extensive resources and expertise, NYU Langone Health aims to contribute significantly to the advancement of medical knowledge and the enhancement of patient care.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
New York, New York, United States
Patients applied
Trial Officials
Milton Biagioni, MD
Principal Investigator
New York University Medical School
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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