Actively Recruiting
Effects of Endogenous Gamma Light Stimulation on Brain Oscillations in Cognitively-normal Older Adults
Led by Chang Gung Memorial Hospital · Updated on 2024-12-04
52
Participants Needed
1
Research Sites
42 weeks
Total Duration
On this page
Sponsors
C
Chang Gung Memorial Hospital
Lead Sponsor
A
Aleddra, Inc.
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study aims to evaluate the effects of endogenous gamma non-flickering light stimulation on resting-state EEG rhythms and cognitive function in cognitively healthy older adults. Specifically, it will assess the immediate and long-term effects of this stimulation on brainwave activity and cognitive performance. The study will explore the potential of gamma light stimulation as a non-pharmacological intervention for cognitive decline in aging populations.
CONDITIONS
Official Title
Effects of Endogenous Gamma Light Stimulation on Brain Oscillations in Cognitively-normal Older Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 55 years old
- Cognitive Abilities Screening Instrument (CASI) score within normal ranges adjusted for age and education
- No history of severe neurological or psychiatric disorders such as stroke, epilepsy, depression, or migraine that could affect cognitive function
- No use of drugs that may affect cognitive function, including benzodiazepines and anticholinergic medications
- Normal or corrected vision using glasses or contact lenses
- Willingness to sign the Informed Consent Form
You will not qualify if you...
- Enrollment in any cognitive enhancement study within the past two months
- History of diseases that could affect cognitive function, such as cancer or autoimmune diseases
- Pregnant or planning to become pregnant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Chang Gung University
Taoyuan, Guishan, Taiwan, 33302
Actively Recruiting
Research Team
C
Chia-Hsiung Cheng, Ph.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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