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Идёт набор NCT03836950

rTMS to Improve Cognition in Parkinson's

Фаза I / Фаза II С лечением Parkinson's Disease Mild Cognitive Impairment

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: MagVenture MagProX100 stimulator (MagVenture, Falun, Denmark), MagVenture MagProX100 stimulator (MagVenture, Falun, Denmark).
Кому может быть актуально
Состояния в реестре: Parkinson's Disease, Mild Cognitive Impairment. Базовые параметры: от 50 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

rTMS as a Cognitive Rehabilitation Approach in Veterans With Parkinson's Disease

Обзор

The purpose of this study is to examine safety, feasibility, and the behavioral and brain effects of a non-invasive treatment, repetitive transcranial magnetic stimulation (rTMS), for Veterans with Parkinson's disease or atypical parkinsonism and mild impairments in their thinking. The hypothesis is that rTMS can improve thinking for people with Parkinson's disease or atypical parkinsonism who are experiencing mild problems with their thinking ability.

Подробное описание

Repetitive transcranial magnetic stimulation (rTMS) shows promise as an effective cognitive neurorehabilitation treatment. To date, no rTMS studies have assessed the effect of rTMS on cognitive function in PD-MCI. Nor has there been PD neurophysiological studies using rTMS to examine neural plasticity in cognitive neural networks. This study seeks to fill this gap by conducting a small scaled pilot randomized controlled trial (RCT) designed to assess the safety and therapeutic effects of rTMS on cognitive outcomes as well as on brain connectivity in Veterans with PD-MCI. PD-MCI participants will be randomized to either active rTMS or sham rTMS. Participants will complete a standardized neurocognitive battery assessment at baseline, endpoint and at a one month follow-up. The primary outcome is change in executive function. Secondary outcomes include performance on other cognitive domain tasks and a proximal measure of real-life function that captures relevant functional changes related to cognitive impairment in PD. Multi-modal neuroimaging, in a subsample of participants, will be used to study neural connectivity changes induced by rTMS. Changes in resting state functional connectivity, grey matter volume via voxel-based morphometry and white matter integrity via diffusion tensor imaging will be assessed at baseline and endpoint. To inform how to optimize rTMS treatment in PD-MCI, these changes will be correlated with changes in cognitive performance.

Вмешательства

  • Устройство MagVenture MagProX100 stimulator (MagVenture, Falun, Denmark)
    The coil will be held tangentially to the skull at approximately 45º from the midline. One rTMS session will consist of 40 trains of 5sec each at 110% of resting motor threshold and 15Hz will be provided at the left DLPFC.
  • Устройство MagVenture MagProX100 stimulator (MagVenture, Falun, Denmark)
    The coil will be held tangentially to the skull at approximately 45º from the midline. The sham coil will not release any stimulation, but it will look, feel and sound like the real rTMS

Первичные конечные точки

  • change in NIH sponsored Executive Abilities: Measures and Instruments for neurobehavioral evaluation and re-search (NIH-EXAMINER) executive composite score [Срок оценки: baseline, 8 weeks, 12 weeks]

Критерии участия

Критерии включения

  • Veterans who seek services at Hines VA Hospital or Jesse Brown VA Medical Center
  • Diagnosis of PD or atypical parkinsonism as determined by a neurologist
  • Meet criteria for having mild cognitive impairment
  • Receiving stable (i.e., no changes in medication and medication dose) medication and who are expected to remain on stable medication for the duration of the RCT
  • Speak and read English
  • 50 years or older

Критерии исключения

  • Dementia
  • Failure to demonstrate decision making capacity
  • History of deep brain stimulation surgery
  • Severe depression
  • Resting head tremor
  • Dyskinesia that will interfere with collecting imaging data
  • Has congestive heart failure
  • Implanted cardiac pacemaker or defibrillator
  • Cochlear implant, nerve stimulator, or intracranial metal clips
  • Implanted medical pump
  • Increased intracranial pressure
  • History of claustrophobia
  • Metal in eyes/face, shrapnel/bullet remnants in brain
  • Participants at potential increased risk of seizure including those who have the following:
  • history (or family history) of seizure or epilepsy
  • history of stroke, head injury, or unexplained seizures
  • presence of other neurological disease that may be associated with an altered seizure threshold
  • such as CVA, cerebral aneurysm, dementia, increased intracranial pressure
  • Concurrent medication use such as tricyclic antidepressants, neuroleptic medications, any other drug known to lower seizure threshold
  • Secondary conditions that may significantly alter electrolyte balance or lower seizure threshold
  • No quantifiable motor threshold such that rTMS dosage cannot be accurately deter-mined

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Четверное слепое
Основная цель
Лечение

Центры проведения

США · 2 центра
  • Jesse Brown VA Medical Center, Chicago, IL — Chicago
  • Edward Hines Jr. VA Hospital, Hines, IL — Hines

Публикации

  • Kletzel S, Alsakaji R, Umbarger A, Walker S, Aaronson A, Herrold A, Colletta K, Bhaumik D, Weaver F, Bender Pape T. Repetitive Transcranial Magnetic Stimulation as a Cognitive Rehabilitation Approach for Veterans With Parkinson Disease and Mild Cognitive Impairment: Protocol for a Randomized Sham-Controlled Trial. JMIR Res Protoc. 2026 Jun 29;15:e77241. doi: 10.2196/77241. PMID 42372258

Идентификаторы

NCT: NCT03836950 · N2938-W · IK2RX002938 · 2023CWR-NDS-831171250

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗