An Empirical Study of the Effects of Memory-Enhancing Eyewear on Sleep and Learning

UMIN ID: UMIN000054604

Registered date:07/06/2024

Basic Information

• Recruitment status: Pending
• Health condition(s) or Problem(s) studied: healthy person
• Date of first enrollment: 2024/06/11
• Target sample size: 26
• Countries of recruitment: Japan
• Study type: Interventional

Intervention(s)

Three types of eyewear are to be worn in order of their assigned type.
Three types of eyewear are to be worn in order of their assigned type.
Three types of eyewear are to be worn in order of their assigned type.

Outcome(s)

• Primary Outcome: 1. To examine the effects of wearing eyewear on sleep by calculating each sleep parameter (total sleep time, sleep efficiency, sleep latency, mid-wake time, total time and percentage of deep sleep time, etc.) when wearing the three types of eyewear, respectively. In addition, parameters related to subjective sleep quality as scored by subjective sleep assessment (OSA-MA) will be calculated and examined respectively. 2. to examine the effects of wearing eyewear on daily changes in concentration and cognitive function.
• Secondary Outcome: 1. To examine changes over time in activity meters and the effects of wearing eyewear. 2. 2. To examine changes in mental health and the effects of wearing eyewear. 3. To examine the subjective evaluation of eyewear use and light intensity.

Key inclusion & exclusion criteria

• Age minimum: 9years-old
• Age maximum: 16years-old
• Gender: Male and Female
• Exclude criteria: 1. Those who regularly consume food for specified health use, functional foods, supplements, or health foods that may affect the study at least 3 times a week, and those who are unable to limit their intake during the study period. 2. Those with a history or current history of serious diseases of the heart, liver, kidney, digestive organs, etc. 3. Persons suspected of having a chronic or acute serious infectious disease. 4. Those who are scheduled to be vaccinated during the study period. 5. Those who have an extremely irregular diet. 6. Those who plan to change their lifestyle drastically during the study period. 7. Who are currently participating in a clinical study of another drug or health food, and who plan to participate in another clinical study within one month after the completion of the study, or after consent to participate in the study. 8.Any other person who is deemed by the principal investigator to be inappropriate to participate in this study.

Related Information

• Primary Sponsor: Mitsui Chemicals, Inc.
• Source(s) of Monetary Support: Mitsui Chemicals, Inc.