Far-Infrared Therapy for the Effect of Alzheimer Disease Dementia

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age61-92
SponsorJuin-Hong Cherng

About this trial

Alzheimer's disease (AD), the most common cause of dementia, is a progressive neurodegenerative disorder characterized by cognitive decline, including impaired learning ability, memory loss, and behavioral disturbances.

According to surveys conducted by the Ministry of Health and Welfare in Taiwan, the prevalence of dementia among individuals aged 65 years and older was estimated at 7.86% in 2018, affecting more than 280,000 individuals, and is projected to approach 900,000 by 2065, resulting in substantial medical, social, and economic burdens. Current pharmacological treatments provide only limited symptomatic benefits and may be associated with adverse effects. Therefore, safe and effective non-pharmacological interventions that may support cognitive function and reduce caregiver burden are urgently needed.

Experimental studies suggest that far-infrared (FIR) irradiation may enhance mitochondrial oxidative phosphorylation, increase ATP production, and promote microglial amyloid-β clearance, which may help delay the progression of Alzheimer's disease.

This trial aims to investigate the safety and effects of far-infrared (FIR) therapy on cognitive function in patients with Alzheimer's disease.

The findings may support the clinical application of FIR therapy as a non-pharmacological intervention to improve cognitive function and quality of life, reduce medication burden and treatment-related side effects, lessen caregiver burden, delay institutionalization, and reduce the social and economic burden associated with Alzheimer's disease.

Eligibility criteria

Qualifiers

Diagnosed with Alzheimer's disease dementia.

Mini-Mental State Examination (MMSE) score between 18 and 24 (inclusive).

Currently prescribed and maintained on a stable regimen of anti-dementia medication.

No sensory deficits or impairment regarding skin temperature perception.

Disqualifiers

Non-Alzheimer's disease dementia (e.g., vascular dementia, Lewy body dementia, frontotemporal dementia).

Known hypersensitivity to heat or light, including the current use of photosensitizing medications.

Diminished thermal or heat sensitivity, such as from the concurrent use of analgesics, sedatives, or consumption of alcoholic beverages.

Acute injury or acute localized inflammation, including active inflammation, infection, or ulcerated wounds.

Trial design

Treatments tested in this trial

  • Yin Fu Rui De Far-Infrared Radiator
  • Sham Far-Infrared Radiator

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Juin-Hong Cherng

Lead sponsor

National Defense Medical Center, Taiwan

Sponsor institution

Tri-Service General Hospital

Collaborator