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 diagnosed with Alzheimer's disease dementia
- People whose memory and thinking test score (called an MMSE score) falls between 18 and 24 out of 30
- People who are currently taking dementia medication and have been on a steady, unchanged dose
- People who have normal ability to feel temperature changes on their skin
- People whose legal representative is willing and able to sign a consent form before the trial begins, or people who are able to sign it themselves
Who may not be able to join:
- People whose dementia is caused by something other than Alzheimer's disease, such as vascular dementia, Lewy body dementia, or frontotemporal dementia
- People who are known to be sensitive or allergic to heat or light, or who are currently taking medications that increase sensitivity to light
- People whose ability to feel heat or temperature is reduced, for example due to taking painkillers, sedatives, or regularly drinking alcohol
- People with a current acute injury, active inflammation, infection, or open wounds
- People with certain active or acute circulatory or joint conditions, including blood clots in a vein, varicose veins, severe blockage of arteries in the limbs, lymphatic disease, active rheumatoid arthritis, active gout, or a current fever
- People with patchy redness or other unusual skin conditions on the scalp or neck
- People with skin lesions, skin damage, or open wounds where the trial device would make contact with the body
- People who are currently taking part in another clinical trial
- People with any other health condition that a doctor determines would make participation unsafe (confirm with trial site)
- People who are unwilling or unable to sign the required consent form
- People who are unable or unwilling to follow the trial schedule, procedures, or required check-up appointments
- People who have a history of, or currently have, a bleeding or blood clotting disorder
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: Jiunn-Tay Lee, Ｍ.D., Trial-Service General Hospital, National Defense Medical University
Phone: 886-2-87923100
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
Number of Participants With Yin Fu Rui De Far-Infrared Therapy Device-Related Adverse Events (AEs); Number of Participants With Yin Fu Rui De Far-Infrared Therapy Device-Related Serious Adverse Events (SAEs)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.