Gamma-Induction in FrontoTemporal Dementia Trial

NCT ID: NCT04425148

Last Updated: 2024-09-26

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 70 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-12-30
• Study Completion Date: 2025-12-31

Brief Summary

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.

Detailed Description

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.

• Electrodes are placed into a cap that you wear on your head.
• A weak electrical current travels back and forth through the electrodes to your head.
• FDG-PET is a way of taking pictures of your brain using a special dye that is absorbed into your body. In this study, the dye will help us to see the glucose uptake in your brain. The PET scans for this study will be done at Massachusetts General Hospital (MGH).
• TMS is a noninvasive way of stimulating the brain and will be used in this study to measure your brain's plasticity. Brain plasticity is the brain's ability to change and learn through experience. TMS uses a magnetic field to cause changes in the brain activity. The magnetic field is produced by a coil that is held next to your scalp. We will measure how your brain responds to the TMS before and after the tACS treatment.
• EEG is used in routine clinical care to measure the brain's electrical activity. EEG involves placing a cap with electrodes onto your head.

The investigators will enroll a sample of 20 age-matched healthy controls, who will undergo evaluations similar to the bv-FTD baseline assessment except for PET imaging. Healthy subjects will not have the tACS intervention.

Conditions

Frontotemporal Dementia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

tACS

40 Hz transcranial alternating current stimulation (tACS), 30 daily (Monday-Friday) 1-hour sessions

Group Type: EXPERIMENTAL

Transcranial Alternating Current Stimulation (tACS)

Intervention Type: DEVICE

tACS is a noninvasive way of stimulating the brain externally using weak electric currents. Electrodes are placed into a cap that you wear on your head. A weak electrical current travels back and forth through the electrodes to your head.

Sham tACS

Sham transcranial alternating current stimulation (tACS), 30 daily (Monday-Friday) 1-hour sessions

Group Type: SHAM_COMPARATOR

Sham Transcranial Alternating Current Stimulation (sham tACS)

Intervention Type: DEVICE

Sham (placebo) simulation of transcranial alternating current stimulation without receiving any real stimulation.

Interventions

Transcranial Alternating Current Stimulation (tACS)

tACS is a noninvasive way of stimulating the brain externally using weak electric currents. Electrodes are placed into a cap that you wear on your head. A weak electrical current travels back and forth through the electrodes to your head.

Intervention Type: DEVICE

Sham Transcranial Alternating Current Stimulation (sham tACS)

Sham (placebo) simulation of transcranial alternating current stimulation without receiving any real stimulation.

Intervention Type: DEVICE

Other Intervention Names

Non-invasive Brain Stimulation; Neuroelectrics Starstim

Eligibility Criteria

Inclusion Criteria

• 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

• 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

• 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

• 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)

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Alzheimer's Drug Discovery Foundation

OTHER

Sponsor Role: collaborator

Massachusetts General Hospital

OTHER

Sponsor Role: lead

Responsible Party

Emiliano Santarnecchi

Associate Professor of Radiology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Emiliano Santarnecchi, PhD

Role: PRINCIPAL_INVESTIGATOR

Massachusetts General Hospital

Locations

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States

Site Status: RECRUITING

Fondazione Santa Lucia

Roma, , Italy

Site Status: RECRUITING

Countries

United States; Italy

Central Contacts

Emiliano Santarnecchi

Role: CONTACT

esantarnecchi@mgh.harvard.edu

617-726-9353

Sara Romanella

Role: CONTACT

sromanella@mgh.harvard.edu

Facility Contacts

Lorella Battelli

Role: primary

lbattell@bidmc.harvard.edu

617-667-9088

Lorella Battelli

Role: backup

Caterina Motta

Role: primary

c.motta@hsantalucia.it

Giacomo Koch, MD

Role: backup

Other Identifiers

2021P003553

Identifier Type: -

Identifier Source: org_study_id