Non-invasive Brain Stimulation for Gamma-induction and Cognitive Enhancement in FTD (Gamma-Induction in FrontoTemporal Dementia, GIFTeD)
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 70
- 试验地点
- 3
- 主要终点
- Change in Gamma activity
研究概览
简要总结
This is an interventional, sham controlled, double-blind study designed to investigate the safety, tolerability and efficacy of 40 Hz transcranial alternating current stimulation (tACS), a form of noninvasive brain stimulation, delivered for 6 weeks once daily in frontotemporal dementia (FTD) patients. Cognition, gamma EEG activity and brain metabolism via FDG-PET will be measured before and after the tACS intervention.
详细描述
This is an interventional, multi-site, randomized, double-blind, placebo-controlled study of tACS in patients with FTD. The main aim of this study is to investigate the safety, tolerability and efficacy of gamma-tACS in patients with behavioral variant (bv)-FTD and semantic variant Primary Progressive Aphasia (svPPA), demonstrating tACS potential mechanisms of action, target engagement, and thus informing the design of larger clinical trials.
Participants will be screened at trial sites for determination of eligibility to enter the study on the basis of diagnostic evaluations, according to current diagnostic criteria for probable bv-FTD and safety assessments.
Baseline assessments will consist of behavioral/cognitive evaluations, blood biomarkers, actigraphy, voice biomarkers, EEG and TMS-EEG and tACS with EEG measures, MRI, FDG-PET imaging (5-8 visits). Once participants have met all inclusion and exclusion criteria, they will be randomly assigned to either 6 weeks of daily tACS sessions or 6 weeks of daily Sham tACS sessions.
Post-intervention visits will include FDG-PET scans, MRI, cognitive testing, tACS with EEG, blood biomarkers and TMS-EEG (5-8 visits). A follow-up visit will occur 3 months after the post-invention visit. This visit will include an EEG registration, cognitive testing and behavioral markers.
- tACS is a way of stimulating the brain externally using weak electric currents.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 40 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Diagnosis of probable Frontotemporal dementia (bvFTD or svPPA)
- •Mini Mental State Examination (MMSE) > 18
- •FTLD-specific Clinical Dementia Rating (FTLD-CDR) total score of ≤1
- •On stable medications related to cognition or behavior for >30 days such as acetylcholinesterase inhibitors, memantine, anti-depressants, antipsychotic agents, other mood stabilizers, benzodiazepines;
- •Age from 40 to 85 years;
- •Minimum of completed 8th grade education
- •No history of intellectual disability
排除标准
- •Current or past history of any significant neurodegenerative disorder of the central nervous system other than FTD e.g. Alzheimer's disease, Lewy body dementia, Parkinson's disease, multiple sclerosis, progressive supranuclear palsy, normal pressure hydrocephalus, Huntington's disease, any condition directly or indirectly caused by Transmissible Spongiform Encephalopathy (TSE), Creutzfeldt-Jakob Disease (CJD), variant Creutzfeldt-Jakob Disease (vCJD), or new variant Creutzfeldt-Jakob Disease (nvCJD);
- •Current or past history of stroke (cortical stroke), intracranial brain lesions, previous neurosurgery or head trauma that resulted in residual neurologic impairment.
- •Non-cortical disease such as confluence white matter changes (including lacunar infarcts < 1cm) and asymptomatic, subacute, cerebellar infarcts may be included upon review of a medically responsible neurologist.
- •Past or current history of major depression, bipolar disorder, psychotic disorders, or any other major psychiatric condition will be evaluated by the study MD.
- •Current history of poorly controlled migraines including chronic medication for migraine prevention
- •History of seizures with the exception of a single seizure of benign etiology (e.g. febrile seizure) in the judgment of the investigator;
- •History of fainting spells of unknown or undetermined etiology that might constitute seizures.
- •Chronic (particularly) uncontrolled medical conditions that may cause a medical emergency in case of a provoked seizure (cardiac malformation, cardiac dysrhythmia, asthma, etc.).
- •Metal implants in the head (except dental), pacemaker, medication pump, nerve stimulator, TENS unit, ventriculo-peritoneal shunt, cochlear implant, unless cleared by the study MD.
- •Contraindication for undergoing MRI or receiving TMS or tACS;
- •Any clinically significant hematological, endocrine, cardiovascular, renal, hepatic, gastrointestinal or neurological disease. If the condition has been stable for at least the past year and is judged by the investigator not to interfere with the patient's participation in the study, the patient may be included;
- •>50 mSv of radiation exposure for research within the past year (PET imaging exclusion);
- •Substance abuse or dependence within the past six months;
- •Medications will be reviewed by the responsible MD and a decision about inclusion will be made based on the following: The patient's past medical history, drug dose, history of recent medication changes or duration of treatment, and combination of CNS active drugs;
- •All female participants that are pre-menopausal will be required to have a pregnancy test; any participant who is pregnant or breastfeeding will not be enrolled in the study;
- •Subjects who, in the investigator's opinion, might not be suitable for the study;
- •A hair style or head dress that prevents electrode contact with the scalp or would interfere with the stimulation (for example: thick braids, hair weave, afro, wig).
- •Healthy Volunteers
- •Inclusion Criteria:
- •Age: 40-85 years
- •Normal healthy volunteer
- •Right-handed (assessed by means of the Edinburgh Handedness Questionnaire)
- •MMSE >27
- •Minimum of completed 8th grade education
- •No history of intellectual disability
- •Exclusion Criteria:
- •History of fainting spells of unknown or undetermined etiology that might constitute seizures
- •History of seizures, diagnosis of epilepsy, history of abnormal (epileptiform) EEG or family history of treatment resistant epilepsy, with the exception of a single seizure of benign etiology (e.g. febrile seizures) in the judgment of the investigator
- •History of head injury resulting in prolonged loss of consciousness
- •Any metal in the brain, skull or elsewhere unless approved by the responsible MD
- •Any medical devices (i.e. Cardiac pacemaker, deep brain stimulator, medication infusion pump, cochlear implant, vagal nerve stimulator) unless otherwise approved by the responsible MD
- •Past or current history of major depression, bipolar disorder or psychotic disorders, or any other major psychiatric condition.
- •Neurological disorder or intracranial lesion (including an incidental finding on MRI)
- •Current history of poorly controlled migraines including chronic medication for migraine prevention
- •Any unstable medical condition
- •Pregnancy
- •Medications will be reviewed by the responsible MD and a decision about inclusion will be made based on the following:
- •The participant's past medical history, drug dose, history of recent medication changes or duration of treatment, and combination with other CNS active drugs.
- •Substance abuse or dependence within the past six months
- •Subjects who, in the investigator's opinion, might not be suitable for the study
- •Diseased or damaged skin over the face or scalp
- •A hair style or head dress that prevents electrode contact with the scalp (for example: thick braids, hair weave, afro, wig)
研究组 & 干预措施
Sham tACS
Sham transcranial alternating current stimulation (tACS), 30 daily (Monday-Friday) 1-hour sessions
干预措施: Sham Transcranial Alternating Current Stimulation (sham tACS) (Device)
tACS
40 Hz transcranial alternating current stimulation (tACS), 30 daily (Monday-Friday) 1-hour sessions
干预措施: Transcranial Alternating Current Stimulation (tACS) (Device)
结局指标
主要结局
Change in Gamma activity
时间窗: up to 6 months
Changes in oscillatory activity in the EEG gamma band will be evaluated before and after the tACS sessions
Change in Brain Metabolism measured via FDG-PET
时间窗: up to 3 months
Change in brain glucose metabolism will be measured via FDG-PET after the daily tACS sessions
Attrition (withdrawal) rate
时间窗: up to 6 months
The rate of enrolled participants who withdraw from the study will be reported
Change in Cognition
时间窗: up to 6 months
Change in Alzheimer's Disease Assessment Scale - Cognitive (ADAS-Cog) score will be reported. The score ranges from 0-85 with the higher score meaning greater cognitive impairment.
次要结局
未报告次要终点
研究者
Emiliano Santarnecchi
Associate Professor of Radiology
Massachusetts General Hospital