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Hyperbaric Oxygen Therapy for Prodromal Alzheimer´s Disease With Cerebrovascular Disease

Hyperbaric Oxygen Therapy for Prodromal Alzheimer´s Disease With Cerebrovascular Disease: A Prospective, Randomized, Double Blind Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05349318
Enrollment
100
Registered
2022-04-27
Start date
2022-03-31
Completion date
2025-03-31
Last updated
2024-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Vascular Disorder, Mild Cognitive Impairment, Prodromal Alzheimer's Disease, Vascular Cognitive Impairment

Brief summary

Alzheimer´s disease is a devastating illness that effects the patients as well as their family members. Its prevalence increases exponentially and the burden on the healthcare system is enormous. AD neuropathology begins 15-20 years before the occurrence of cognitive symptoms, which ranges from preclinical stage to mild cognitive impairment (MCI) to dementia. Prodromal AD is an early stage of the disease which is characterized by positive biomarkers and MCI. To this day, there is no medication that can cure or halt the progression of the disease and most studies focus on finding reversible risk factors and changing their influence. Several aetiologies have been proposed, like the deposition of amyloid and tau proteins, neuroinflammation and cerebral ischemia due to cerebrovascular factors. The Amyloid deposition, which serves as the biological marker of AD, was originally thought to be the main cause of the disease, however, recent data suggests that it is not the cause and that it might actually has a protective role. On the other hand, it is known today that vascular changes with related tissue ischemia and neuroinflammation have a crucial role in the development of AD in many patients. These pathologies, ischemia & neuroinflammation, can be improved by the use of hyperbaric oxygen therapy (HBOT). The goal of this study is to explore the potential beneficial effect of HBOT on prodromal AD.

Detailed description

Alzheimer disease is characterised by cognitive, mental and functional disability that is expected to progress until the patient is fully dependent on others for activities of daily living. The pathology begins many years until the cognitive symptoms appear. Prodromal Alzheimer's disease is a state where a person has mild cognitive impairment and Amyloid deposition, which is seen on brain Amyloid PET or in lumbar puncture. To date, there has been neither a cure nor a therapy that can significantly halt or relieve symptoms for most patients. This study offers a new biological therapeutic approach aimed to induce neuroplasticity and improve neurological and cognitive functions. Pre -clinical as well as clinical data indicate that HBOT can be beneficial for those patients who suffer from MCI due to Alzheimer's disease and also to patients with cerebral vascular disease. HBOT is a well-known treatment used in clinical practice for other indications and is considered to be safe with relative rare mild and reversible side effect .The study is designed as a prospective, randomized, sham controlled double blinded study. Subjects will be enrolled up to a total of 100 subjects, age 60-85, diagnosed with MCI and positive Amyloid PET and vascular changes on brain MRI. Eligible patients will be randomized to the two study groups at a ratio of 6:6 (in clusters of 6 patients). The HBOT/sham treatment includes 60 daily sessions of 90 minutes each, five days per week. After the treatment period, there will be a maintenance period of HBOT/sham sessions twice a week for 6 months. All assessments with be done on baseline, after the treatment period and after the maintenance period. The primary endpoint includes improvement in cognitive scores in neurocognitive evaluations (Neurotrax). Secondary and tertiary endpoints include changes in cognitive, physiological, physical, imaging, lab tests and self report questionaires.

Interventions

DEVICEHyperbaric oxygen therapy

Each session will include exposure of 90 minutes to 100% at 2 ATA, with 5 minutes air breaks every 20 minutes

DEVICESham

Each session will include exposure of 90 minutes to 21% at 1.2 ATA during the first five minutes of the session with the noise of circulating air, and then decrease slowly during the next five minutes to 1.03 ATA

Sponsors

Assaf-Harofeh Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Eligible candidates will be randomized with equal probability to the HBOT and sham interventions. Randomization will be performed using a computer software based on patients' code. Since the HBOT chamber can hold six subjects, the randomization will be done in clusters of six patients. After randomization, when a cluster of six subjects from one of the arms will be filled, the intervention for that cluster will begin. Three study technicians will be the only unblinded staff who have the key for the group assignment of each subject. They will exclusively activate the HBOT/sham protocol during session times. All subjects and other clinic staff will remain blinded to the group assignments.

Intervention model description

Upon consent and evaluation, eligible participants will be randomized with equal probability into one of two arms: HBOT or SHAM. The evaluation procedure will be performed at baseline, after the treatment and after a maintenance period.

Eligibility

Sex/Gender
ALL
Age
60 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

1. Diagnosis of Mild cognitive impairment (MCI) due to AD or mixed AD and vascular dementia pathology 2. MMSE score of 20 and above 3. Stable psychological and pharmacological treatment for more than three months prior to inclusion. 4. Caregiver that is seeing the patient at least twice per week and is willing to participate and accompany the patient and fill questionnaires 5. Subject willing and able to read, understand and sign an informed consent

Exclusion criteria

1. Inability to attend scheduled clinic visits and/or comply with the study protocol 2. History of traumatic brain injury, brain tumors, brain surgery, chronic subdural haemorrhages, Epilepsy 3. Active malignancy 4. Substance use at baseline, except for prescribed cannabis if vaporized or taken PO as tincture 5. History of other neurodegenerative diseases including Parkinson's disease (PD), Lewy body dementia (LBD), Frontotemporal dementia (FTD), Multiple sclerosis (MS), Amyotrophic lateral sclerosis (ALS), Creutzfeld Jacob disease (CJD), Multisystem atrophy (MSA), Pseudobulbar palsy (PSP), Corticobasal degeneration (CBD), Wernicke Korsakoff syndrome 6. Chronic use of medications that may compromise cognitive function and cannot be stopped: Anticonvulsants, Anticholinergics, antiparkinsonian, corticosteroids, Benzodiazepines 7. Moderate to severe sleep apnea with no use of CPAP 8. Diagnosis of a psychiatric disorder including: major depression, schizophrenia, bipolar disorder 9. Serious suicidal ideation 10. Renal or liver insufficiency, electrolyte imbalances 11. Chronic heart failure with ejection fraction of 35 or less 12. HBOT for any reason prior to study enrolment 13. Chest pathology incompatible with pressure changes (including active asthma or COPD) 14. Ear or Sinus pathology incompatible with pressure changes (above 3 otolaryngologist visits a year) 15. An inability to perform an awake brain MRI or Amyloid PET 16. An inability to perform computerized cognitive tests (Neurotrax) 17. MMSE score below 20 18. No evidence of amyloid in the brain PET 19. No evidence of vascular related lesions in the brain MRI 20. Active smoking 21. Participation in another study

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline of neurocognitive functions evaluation by Mindstreams cognitive battery test (Neurotrax)At baseline, 3 monthsMemory, attention and information process will be evaluated using the NeuroTrax computerized cognitive evaluation battery.

Secondary

MeasureTime frameDescription
Brain functional connectivity imagingAt baseline ,3 months, 9 monthsResting state functional MRI
Brain amyloid PET using Flumetamol (Vizamyl) tracerAt baseline, 3 months, 9 monthsBrain amyloid assessment using PET scan with Flumetamol (Vizamyl) tracer will be used to assess change in amyloid burden
Whole-brain quantitative perfusion imagingAt baseline, 3 months, 9 monthsWhole-brain quantitative perfusion imaging will be performed using Dynamic susceptibility contrast (DSC)-MRI technique
Brain microstructure MRI evaluationAt baseline, 3 months, 9 monthsFractional anisotropy (FA) and Mean diffusivity (MD) will be evaluated using diffusion tensor imaging (DTI) MRI protocol
Brain volume MRI evaluationAt baseline, 3 months, 9 monthsGray matter and hippocampal volumetric measurement using high-resolution MP-RAGE 3D MRI

Other

MeasureTime frameDescription
Advanced Activities of Daily Function (a-ADL)At baseline, 3 months, 9 monthsQuestionnaire of activities of daily living for the patient and the informant
Clinical Dementia Rating (CDR) scale - sum of boxesAt baseline, 3 months, 9 monthsCognitive assessment of 6 cognitive and functional domains, based on an interview of the patient and a reliable informant
Montreal Cognitive Assessment (MOCA)At baseline, 3 months, 9 monthsNeurocognitive assessment
Mini Mental State Exam (MMSE)At baseline, 3 months, 9 monthsNeurocognitive assessment
Serum inflammatory markersAt baseline, 3 months, 9 monthsSerum inflammatory markers include: IL-1, IL-6, tumor necrosis factor-alpha, hsCRP
Alzheimer's disease (AD) biomarkers: Abeta 42/40At baseline, 3 months, 9 monthsPlasma will be tested for Abeta 42/40
Alzheimer's disease (AD) biomarkers: P-tau181At baseline, 3 months, 9 monthsPlasma will be tested for P-tau181
Alzheimer's disease (AD) biomarkers: P-tau231At baseline, 3 months, 9 monthsPlasma will be tested for P-tau 231
Alzheimer's disease (AD) biomarkers: neurofilament light (NfL)At baseline, 3 months, 9 monthsPlasma will be tested for neurofilament light (NfL)
Alzheimer's disease (AD) biomarkers: plasma glial fibrillary acidic protein (GFAP)At baseline, 3 months, 9 monthsPlasma will be tested for plasma glial fibrillary acidic protein (GFAP)
Vascular biomarker- Vascular endothelial growth factor (VEGF)At baseline, 3 months, 9 monthsSerum will be tested for VEGF
Passive behavioral monitoring using BHQ smartphone applicationThrough study completion, up to one yearAn application will be installed on the participants' smartphones for continuous passive monitoring of human behavior
Cardiopulmonary exercise test (CPET)At baseline, 3 months, 9 monthsCPET determines the anaerobic threshold that is expected to change through the intervention
Neuro-physical evaluation - Static balanceAt baseline, 3 months, 9 monthsStatic balance will be assessed by the Balance Error Scoring System (BESS)
Neuro-physical evaluation- Timed Up and Go testAt baseline, 3 months, 9 monthsDynamic balance and risk of falling will be assessed by the Timed Up and Go test (TUG)
Neuro-physical evaluation - 10 meter walkAt baseline, 3 months, 9 monthsDynamic balance and risk of falling will be assessed by 10-meter walk (10MW).
Neuro-physical evaluation - Sit to Stand testAt baseline, 3 months, 9 monthsMuscle function will be assessed by the sit to stand (STS) test for the leg strength and endurance
Neuro-physical evaluation - Hand held dynamometeryAt baseline, 3 months, 9 monthsMuscle function will be assessed by the hand-held dynamometry (HHD) for the isometric grip strength.
Neuro-physical evaluation - 6 minute walkAt baseline, 3 months, 9 monthsThe sub-maximal aerobic capacity and endurance will be assessed by the 6-minute walk test (6MWT).
Event-related synchronization (ERS) change - EEGAt baseline, 3 months, 9 monthsThe EEG will include a three-level visual N-back task, and go-no-go task
Event-related desynchronization (ERD) change - EEGAt baseline, 3 months, 9 monthsThe EEG will include a three-level visual N-back task, and go-no-go task
Grand average P300 ERP change - EEGAt baseline, 3 months, 9 monthsThe EEG will include a three-level visual N-back task, and go-no-go task
Alpha band power change - EEGAt baseline, 3 months, 9 monthsThe EEG will include a three-level visual N-back task, and go-no-go task
Delta band power change - EEGAt baseline, 3 months, 9 monthsThe EEG will include a three-level visual N-back task, and go-no-go task
Theta to alpha bands power ratio change - EEGAt baseline, 3 months, 9 monthsThe EEG will include a three-level visual N-back task, and go-no-go task
N-back match/no match percentage change - EEGAt baseline, 3 months, 9 monthsThe EEG will include a three-level visual N-back task, and go-no-go task
Gamma band power change - EEGAt baseline, 3 months, 9 monthsThe EEG will include a three-level visual N-back task, and go-no-go task
Beta band power change - EEGAt baseline, 3 months, 9 monthsThe EEG will include a three-level visual N-back task, and go-no-go task
Quality of life SF-36 questionnaireAt baseline, 3 months, 9 monthsSelf reported SF-36 quality of life questionnaire
The Pittsburgh Sleep Quality Index (PSQI) questionnaireAt baseline, 3 months, 9 monthsSelf reported quality of sleep questionnaire
The Depression, Anxiety and Stress Scale-21 (DASS-21)At baseline, 3 months, 9 monthsSelf reported questionnaire of depression, anxiety and stress

Countries

Israel

Contacts

Primary ContactKarin Elman Shina, MD
karine@shamir.gov.il0097289778061

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026