Effects of Far Infrared Radiation Air Conditioning on Sleep

Not Applicable

• Conditions: Healthy adults

• Registration Number: JPRN-UMIN000050083
• Lead Sponsor: MIYA JAPAN.CO.,LTD

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-01-19
• Study Completion: 2023-09-30
• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Not provided

Exclusion Criteria

-Subjects who are currently receiving treatment (including medication) for any disease. -Subjects who have been diagnosed with sleep disorders such as insomnia or sleep apnea syndrome and are taking drugs such as sleep inducers or insomnia medications (including OTC drugs as well as prescription drugs) or are receiving treatment with CPAP or mouthpieces, etc. -Those who regularly use foods for specified health use, functional foods, supplements, or health foods (GABA-containing foods, lactic acid bacteria drinks, theanine-containing foods, crocetin-containing foods, polyphenol-containing foods, etc. that claim to improve sleep) that may affect the research at least 3 times a week. Subjects who regularly consume GABA-containing foods, lactic acid bacteria beverages, theanine-containing foods, crocetin-containing foods, polyphenol-containing foods, etc.) three or more times a week, and who are unable to limit their intake during the study period -Subjects suspected of having a chronic or acute serious infectious disease -Subjects who are scheduled to be vaccinated during the study period -Subjects who work late at night or in shift work -Subjects who habitually drink alcohol more than 3 times a week and more than 1 sake equivalent (beer: 1 medium bottle, whiskey: 1 double, shochu: 0.6 sake) -Subjects with extremely irregular eating habits -Subjects with a BMI of 30 or higher -Subjects who are currently participating in a clinical study of other drugs or health foods, and who are scheduled to participate in another clinical study within one month after the completion of the study or after consent to participate in the study. -Subjects who are unable to stay at the designated research site for a certain period of time -Subjects who are otherwise deemed by the Principal Investigator to be inappropriate for participation in this study.

Study & Design

• Study Type: Interventional
• Study Design: Not specified