Early Alzheimer's Disease
Conditions
Interventions
Perform 3 sets every other day, 3 times a day for 20 minutes each time (at intervals of 5 minutes or more between each session). Considering this as one course, one course (weeks 0, 12, 24, 36, 48, an
Sponsors
Shimokawa Hiroaki
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Provide written informed consent to participate in the clinical trial from the patient and their legal representative. 2) Mild AD or MCI due to AD patient aged greater than or equal to (>=) 50 and less than (=20 at screening. 7) No organic diseases such as symptomatic cerebral hemorrhage, symptomatic cerebral infarction, acute cerebral infarction, brain tumor, etc. within 48 weeks before obtaining informed consent or in head MRI images at screening, and in head MRA images, Patients evaluated by the imaging evaluation committee as not having severe stenosis/occlusion from the internal carotid artery to the middle cerebral artery. 8)Patients who are receiving existing drug therapy for Mild AD or MCI due to AD and are not scheduled to change their medication within the past 4 weeks from obtaining consent and after obtaining consent.
Exclusion criteria
Exclusion criteria: 1) Patients judged by the investigator that it is difficult to continue the study treatment for 20 minutes. 2) Patients judged by the investigator to be difficult to perform an MRI examination. 3)Patients with impaired consciousness with a GCS score of 12 or less at the time of enrollment. 4) Patients who have had symptomatic cerebral infarction or cerebral hemorrhage within 12 weeks prior to enrollment. 5) Patients with a modified Hachinski Ischemic Scale score of 5 or more at enrollment. 6) Patients with Lewy body dementia and frontotemporal dementia. 7) Patients judged by the investigator to be difficult to participate in the clinical trial due to severe mental illness. 8) Poorly controlled serious systemic disease (heart failure, liver failure, renal failure, vitamin B12 deficiency, hypothyroidism, etc.) that makes it difficult for the investigator to participate in the study judged patient. 9)Patients with uncontrolled diabetic retinopathy (with active fundus hemorrhage). 10)Patients who have malignant tumor as a complication or who have been treated for malignant tumor within 5 years from the time of enrollment (excluding cured resected carcinoma in situ). 11) Patients who are or have a history of drug addiction or alcohol addiction. 12) Patients with or with a history of epilepsy. 13)Patients with implants such as coils, electrodes and stents in the skull. 14) Patients within 5 years after brain surgery (including endovascular treatment). 15) Patients who are pregnant or wish to become pregnant. 16) Patients participating in other clinical studies (excluding non-interventional observational studies) or clinical trials. 17) Patients who are otherwise judged to be ineligible by the investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in ADAS-J-cog-14 scores from baseline to 72 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| '- Changes in ADAS-J-cog-14 scores from baseline to 24 and 48 weeks. - Changes in CDR-SB from baseline to 48 and 72 weeks. - Changes in MMSE-J, FAQ, NPIQ-J, J-ZBI, WMS-R, EQ-5D-5L and ABC from baseline to 24, 48 and 72 weeks. - Prevalence of responders at 24, 48, and 72 weeks defined as those with no deterioration or even improvement in ADAS-J-cog-14 scores. - Transition rate from MCI due to AD to AD at 72 weeks. - The safety endpoints include adverse symptoms until 72 weeks and any abnormal MRI findings at 72 weeks. - Termination due to aggravation of dementia symptoms. | — |
Contacts
Public ContactClinical trials information
Sound Wave Innovation CO., LTD.
Outcome results
None listed