Healthy subjects
Conditions
Interventions
Group A (Lead-in Intervention Group): Intervention (wearing the test product) will be conducted for 6 months immediately following the pre-study survey, followed by a 6-month optional wearing period (
Sponsors
Macromill, Inc.
Saitama Prefectural University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1)Persons engaged in work at medical institutions 2)Persons who have received a sufficient explanation of the purpose and content of the study and have consented to participate of their own free will
Exclusion criteria
Exclusion criteria: 1)Persons at risk of showing allergic symptoms due to the materials of the research products 2)Persons who cannot follow the instructions of the principal investigator, or those whom the principal investigator deems inappropriate 3)Others whom the principal investigator deems ineligible as study subjects
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Labor productivity (Amount of loss) | — |
Secondary
| Measure | Time frame |
|---|---|
| Somatic Symptom Scale, Sleep quality, Depression risk, Work engagement | — |
Countries
Japan
Contacts
Public ContactKenta Ochiai
Macromill, Inc. Clinical Trial Department, Life Science Division
Outcome results
None listed