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:
- You have been diagnosed with probable Alzheimer's disease (AD) with mild cognitive impairment, based on 2024 guidelines, OR you have been diagnosed with a type of frontotemporal dementia (a condition affecting behaviour or language).
- Test results (from a brain scan or spinal fluid test) show abnormal amyloid protein buildup in the brain — this is a marker linked to Alzheimer's disease (confirm with trial site).
- Test results (from a brain scan or spinal fluid test) show abnormal tau protein in the brain — another marker linked to Alzheimer's disease (confirm with trial site).
- If you have Alzheimer's disease, you have been taking standard Alzheimer's medications at the same dose for at least 12 weeks before the study starts.
- If available, genetic test results confirming a frontotemporal dementia-related gene mutation may be included (this appears to be optional — confirm with trial site).
- You are between 45 and 85 years old; there is no restriction on gender.
- You are right-handed.
- You have had at least 3 years of formal education.
- You scored 11 or higher on a standard memory and thinking test called the MMSE (confirm with trial site).
- You have a CDR score of 1 or 2, meaning your dementia is in the mild to moderate range (confirm with trial site).
- You have a reliable caregiver who can support your participation.
- You are able to take part in thinking and memory tests and training activities.
- You fully understand the study, are willing to take part voluntarily, and can sign a consent form approved by an ethics committee.
Who may not be able to join:
- You have been diagnosed with another type of dementia or a major brain or nervous system condition, such as stroke, epilepsy, Lewy body dementia, vascular dementia, Parkinson's disease dementia, or Huntington's disease.
- You have a significant mental health condition, such as severe depression or severe anxiety.
- You have serious problems with your heart, liver, or kidneys (for example, advanced heart failure, liver cirrhosis, or kidney failure).
- You take medications that are known to significantly affect memory or thinking (such as certain sedatives or specific bladder medications), unless your doctor has approved them.
- You have metal implants in your body that are not safe for MRI scans or a specific type of brain stimulation used in this trial, such as a pacemaker or deep brain stimulator.
- You have defects or abnormalities in your skull.
- You are unable to tolerate wearing an EEG cap (brain activity recording device) or keeping your head still during procedures.
- You have severe vision or hearing problems that would prevent you from completing the study tasks.
- You have a history of alcohol or drug misuse.
- You have taken part in another clinical trial within the past 3 months.
- You are currently receiving or have recently received treatment with certain newer Alzheimer's drugs called anti-amyloid antibodies (for example, lecanemab or donanemab).
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
Phone: +86 18959257015
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
Changes from Baseline in Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog) Score
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.