Fact CheckerSign in

NCT06715995Recruiting

Effects of Endogenous Gamma Light Stimulation on Brain Oscillations in Cognitively-normal Older Adults

Effects of Endogenous Gamma Light Stimulation on Brain Oscillations in Cognitively-normal Older Adults: a Randomized, Placebo-controlled, Double-blind Study

Source: ClinicalTrials.gov · Last updated 4 Dec 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
52 (estimated)
First submitted
28 Nov 2024
Start date
9 Dec 2024
Primary completion date
30 Sept 2025
Lead sponsor
Chang Gung Memorial Hospital
NCT number
NCT06715995

What you commit to

  • Study type: Interventional
  • Planned participants: 52
  • From 9 Dec 2024 to the primary completion date, 30 Sept 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 2\. Participants with a history of disease that could affect cognitive function (e.g., cancer, autoimmune diseases, etc.).

Other

  • 1\. Participants enrolled in any cognitive enhancement study within the past two months.
  • 3\. Pregnant, or planning to become pregnant.

Who the study is looking for

  • 1\. Age over 55 years old.
  • 2\. The Cognitive Abilities Screening Instrument (CASI) score is within normal ranges adjusted for age and education.
  • 3\. Participants have no history of severe neurological or psychiatric disorders (such as stroke, epilepsy, depression, migraine, etc.) that could affect cognitive function.
  • 4\. Participants have not used drugs that may affect cognitive function (e.g., benzodiazepines, anticholinergic medications, etc.).
  • 5\. Participants with normal or corrected vision (e.g., glasses or contact lenses) to normal levels.
  • 6\. Voluntary to sign the Informed Consent Form.

Age in the registry: 55 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chang Gung University
Coordinator of this site? Confirm its status
TaoyuanTaiwanRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.