Efficacy test of daytime rest habits
Not Applicable
- Conditions
- Healthy subjects
- Registration Number
- JPRN-UMIN000045619
- Lead Sponsor
- Kao Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 400
Inclusion Criteria
Not provided
Exclusion Criteria
-Subjects with diseases, inflammation, wounds, swelling, eczema, etc. around eyes -Subjects who are conscious of being sensitive to warmth -Subjects who are aware of the decrease in warm sensation -Subjects who are not good at menthol stimulation -Subjects have difficulty to treat hot fomentation on eyes in the daytime -Pregnancies and lactations -Subjects deemed inappropriate to participate in this study by the principle investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluation of the changes of ophthalmologic complaint, labor productivity, QOL, and working time after repeated treatment for 1week or 1week and 1month with hot fomentation on eyes.
- Secondary Outcome Measures
Name Time Method -Analysis of the degree of eye complaint or improvement, personality, community site participation status, and the habitation of daytime rest -Changes in stress level and presentism in 2021 and 2022