Alzheimer's Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been taking an acetylcholinesterase inhibitor (a common Alzheimer's medication) for at least 2 months before joining, and whose dose can stay the same throughout the trial.
- People aged 60 to 85 years, either male or female.
- People who have been diagnosed with mild-stage Alzheimer's Disease using recognised diagnostic guidelines (NIA-AA 2011).
- People whose Alzheimer's disease has been confirmed by a type of brain scan called an amyloid PET-CT.
- People whose score on a standard memory and thinking test (called the MMSE) falls between 21 and 26.
- People whose score on either the CDR (a dementia rating scale) is 1, or whose score on the GDS (another rating scale) is 3.
- People who are found to be physically suitable to take part, based on their medical records and a physical check-up.
- People who are not able to give consent on their own due to difficulties with decision-making, but whose legally authorised representative can give consent on their behalf, and who can attend appointments with a caregiver present.
- People who agree to take part in all visits and activities over the full 24-week trial period.
- People with normal ability to see and read text, and to hear.
- People whose first language (mother tongue) is Korean.
Who may not be able to join:
- People who have other brain or nervous system conditions that could explain their memory and thinking difficulties — such as vascular dementia, brain tumours, brain infections, Parkinson's disease, Huntington's disease, head injury, or similar conditions.
- People who have lost consciousness due to brain surgery or a concussion, or who show signs of increased pressure in the skull on neurological examination.
- People with a history of epilepsy or epileptic seizures.
- People who have had a history of drug or alcohol misuse at any point in the 5 years before screening.
- People with certain mental health conditions, including schizophrenia, schizoaffective disorder, bipolar disorder, a current major depressive episode, psychosis, panic disorder, post-traumatic stress disorder, severe anxiety, intellectual disability, or other conditions classified under DSM-V (confirm with trial site).
- People with abnormal vitamin B12, folic acid, or thyroid hormone test results that the investigating doctor believes are affecting, or are caused by, the severity of their dementia.
- People who have certain metal implants in the head, such as cochlear implants, brain stimulators, or aneurysm clips (confirm with trial site regarding exceptions).
- People who have a cardiac pacemaker.
- People who have an implanted medication pump.
- People who have intracardiac lines (tubes or devices placed inside the heart).
- People who are currently taking medications that lower the threshold for seizures (make seizures more likely).
- People with significant heart disease.
- People with severe kidney or liver disease that meaningfully affects daily life — for example, stage 4 chronic kidney disease — as judged by the investigating doctor.
- People for whom having an MRI scan would not be safe or suitable.
- People for whom having an amyloid PET-CT scan would not be safe or suitable.
- People who do not agree to receive TMS (a type of brain stimulation) treatment or to take part in the trial.
- People who have taken part in another clinical trial within the 3 months before joining this one (note: non-interventional studies such as observational studies may be acceptable — confirm with trial site).
- People who have received TMS treatment at any point in the 2 years before joining this trial.
- People with a history of a malignant tumour (cancer) within the last 5 years — though participation may be considered if more than 5 years have passed since the cancer was declared fully treated and there has been no recurrence.
- People who need to take any medications that are listed as prohibited alongside this trial's treatment (confirm specific medications with trial site).
- People who the investigating doctor considers unsuitable for any other reason.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Ae Young MD LEE, PhD, Chungnam National University Hospital
Phone: +82314450566
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Alzheimer's Disease Assessment Scale-Cognition Score (Efficacy)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.